Impact of Medically Supervised Performance-Enhancing Substances (PES) on Elite Athletes (ASCEND001)
Impact of Medically Supervised Performance-Enhancing Substances (PES) on Elite Athletes: A Hybrid Design in a Real-World Setting
Objectives:
The primary objective is to assess the safety and tolerability of medical drugs with the potential to enhance performance (PES) in professional athletes over a 5.5 year period, encompassing a 25-week PES Exposure period and 5 year long term follow-up of period comprehensive health and safety monitoring. The secondary objective is to evaluate the impact of PES on athletic performance through validated sport specific and clinical assessments.
Methods:
This prospective hybrid design study will enrol 60 adult participants, divided into two groups. The first group will receive performance-enhancing substances (PES) directly through the study, administered as Investigational Medicinal Products (IMPs) under comprehensive medical supervision for up to 25 weeks. The second group will include natural athletes and those already using PES prescribed by their own doctors. All substances used in this study are medically approved by national regulatory agencies (e.g., FDA, MHRA, EMA, EDE, etc.), and market authorised.
Participants undergo enrollment and baseline health and performance assessments, prior to a 25 weeks of PES exposure. During the period of PES exposure, participants undergo periodic monitoring of comprehensive physiological biomarkers alongside subjective assessments. Following the PES exposure phase, participants will complete repeat baseline health and performance assessments, followed by a titration phase and, where indicated, post-cycle therapy (PCT) to support the restoration of physiological function toward baseline. The study will conclude with a five-year longitudinal follow-up period to monitor long-term health outcomes. During this phase, participants will undergo annual assessments, including cardiac electrocardiography (ECG), echocardiography, magnetic resonance imaging (MRI), blood and urine biomarkers, routine vital signs, and quality-of-life measures. Additional imaging will include brain functional MRI (fMRI) and vital organ ultrasound at years 1, 3, and 5, with cardiac CT performed as clinically indicated. Athlete safety biomarker assessments, clinical evaluations, and adverse event reporting, will be continuously evaluated by study doctors and with additional safety oversight from a Data Safety Monitoring Board, Independent Medical Commission (a multidisciplinary panel of medical experts), and a Medical Monitor.
研究概览
地位
干预/治疗
- 药品:Testosterone Enanthate
- 药品:Testosterone Cypionate
- 药品:Testosterone Propionate
- 药品:Sustanon (testosterone)
- 药品:Testosterone Gel
- 药品:Methenolone Enanthate (Primobolan)
- 药品:Nandrolone Decanoate (Deca-Durabolin)
- 药品:Estradiol Patch
- 药品:Estradiol Capsule
- 药品:Progesterone Cream
- 药品:Progesterone Capsule
- 药品:Human Growth Hormone (hGH)
- 药品:EPO Darbepoetin (Aranesp)
- 药品:Meldonium
- 药品:Modafinil
- 药品:Mixed amphetamine salts (Adderall)
- 药品:Clomiphene
- 药品:Anastrozole
- 药品:Levothyroxine
- 药品:Liothyronine
- 药品:hCG
- 药品:hMG
- 药品:Atorvastatin
- 药品:Rosuvastatin
- 药品:Bisoprolol
- 药品:Nebivolol
- 药品:Metoprolol
- 药品:Propranolol
- 药品:Lisinopril
- 药品:Enalapril
- 药品:Furosemide
- 药品:Chlorothiazide
- 药品:Cabergoline
- 药品:Metformin
- 药品:Basal Insulin Glargine (long-acting)
- 药品:Telmisartan
- 药品:Losartan
详细说明
研究类型
注册 (估计的)
阶段
- 不适用
联系人和位置
学习地点
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Abu Dhabi、阿拉伯联合酋长国
- Clinical Trial Site
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参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
Inclusion Criteria:
Participants are eligible to be included in the study only if all the following criteria apply:
- Participant must be 18 years of age or older at the time of signing the informed consent.
- Capable of giving signed informed consent, which includes compliance with the requirements and restrictions listed in the ICF and in this protocol.
- For a participant that intends to and uses PES as part of the study, the participant must be retired from professional sporting organizations that prohibit the performance enhancing substances and substances studied and must not be subject to active anti-doping regulations or testing pools at the time of enrollment.
- Participant must be under the care of a primary care provider (PCP).
- Participant passes medical profiling assessment (measuring overall state of health and quality of life)
Females must meet one of the following:
- Postmenopausal (>45 years of age with amenorrhea for at least 12 months, without using exogenous hormonal contraception and with FSH ≥ 40 IU/L).
- Surgically sterile (hysterectomy, bilateral salpingectomy; oophorectomy) for at least 6 months.
- Using a double contraception including a barrier method (condom, diaphragm, or occlusive cap) and a highly effective method of birth control, which includes the following:
i. Established use (i.e. at least 90 days prior to signing of ICF) of combined (estrogen and progestogen) oral, intravaginal, or transdermal hormonal contraceptive associated with inhibition of ovulation. ii. Established use (i.e. at least 90 days prior to signing of ICF) of progestogen- only oral, injectable, or implantable hormonal contraceptive associated with inhibition of ovulation.
iii. Established use (i.e. at least 90 days prior to signing of ICF) of an intrauterine device (IUD) or intrauterine hormone-releasing system (IUS).
iv. Bilateral tubal occlusion completed at least 90 days prior to signing of ICF.
d) Vasectomized partner with the appropriate post-vasectomy documentation of the absence of spermatozoa in the ejaculate. Participant must provide documentation before the first dose of PES.
e) Sexual abstinence, when this is in line with the preferred and usual lifestyle of the participant.
Exclusion Criteria:
Participants are excluded from the study if any of the following criteria apply:
A self-reported history of any significant psychological or psychiatric challenges that may affect their ability to safely engage in the study or comply with study procedures. This includes, but is not limited to:
- Ongoing or recently unstable conditions such as severe depression or other psychiatric disorders that have not been effectively managed, in the judgement of the clinical research team.
- A history of severe mental health conditions (e.g., schizophrenia, bipolar disorder) that have required intensive intervention or hospitalization within the past 5 years.
- Prior history of malignancy (including breast cancer, lymphoma, leukemia) within the past 5 years except for cervical or prostate carcinoma in situ that has been completely resected or cured basal or squamous cell skin carcinoma.
Has a history of CV disease that includes any of the following:
- Unstable CV disease, myocardial infarction, unstable angina, cardiac bypass or coronary arteries stenting, cerebrovascular accident (stroke), or transient ischemic attack.
Clinically significant cardiac arrhythmias, including congenital arrhythmia syndromes (e.g. Long QT syndrome, Brugada Syndrome) or acquired arrhythmias, including pacemaker or ICD.
Note. Cases will be considered on a case-by-case basis following an expert sports cardiology review using the newest internationally published recommendations.
- Congestive heart failure (New York Heart Association class II to IV symptoms) or inherited or acquired cardiomyopathies Note. Cases will be considered on a case-by-case basis following an expert sports cardiology review using the newest internationally published recommendations.
- Current or history of clinically significant (per Investigator's judgment) liver or biliary disease.
- Current acute or chronic self-reported HCV and/or HBV infection.
- Current or history of clinically significant renal disease (per Investigator's judgment) or GFR <60mL/min/1.73m2
- Has history or presence of any results from Screening Visit laboratory tests, ECG, physical examination, or vital signs that, in the opinion of the Investigator, Medical Monitor, or Sponsor, should be exclusionary for such a candidate.
The use of other investigational drugs at the time of screening or within 30 days or 5 half- lives prior to signing of the ICF, whichever is longer, or longer if required by local regulations.
Note. Upon entry into the long-term follow-up phase of the study, participation in another clinical trial may be permitted only if it does not interfere with the objectives of this study. This is at the discretion of the study Investigator.
- Pregnant or breastfeeding.
- Has a mental or legal incapacity.
- Is unwilling to provide written informed consent or is unable to follow the procedures outlined in the Protocol.
Prospective approval of protocol deviations to recruitment and eligibility criteria, also known as protocol waivers or exemptions, is not permitted.
学习计划
研究是如何设计的?
设计细节
- 主要用途:其他
- 分配:非随机化
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
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无干预:Group 1: Natural and independently enhanced athletes (Observation Group)
These study participants will either not use any PES (natural) or will use their own PES according to their own schedule (independently enhanced).
These participants will not receive any study-provided PES and will have fewer site visits.
They will be monitored via a virtual check-in every 4 weeks, primarily to collect safety data.
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实验性的:Group 2: Enhanced-PES (Intervention Group)
These study participants will follow one (or more) PES regimens developed by the Sponsor.
The study team will work closely with each participant and leverage all available medical and performance data to help plan the optimal PES strategy (or strategies) to ensure safety and tolerability and maximize athletic performance.
This study utilizes FDA-approved, market-authorized substances within a prospective, observational case series design and does not constitute a phase-based clinical trial investigation of these products.
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Intramuscular injection administered for up to 25 weeks
Intramuscular injection administered for up to 25 weeks
Intramuscular injection administered for up to 25 weeks
Intramuscular injection administered for up to 25 weeks
Topical gel administered for up to 25 weeks
Intramuscular injection administered for up to 25 weeks
Intramuscular injection administered for up to 25 weeks
Topical patch administered for up to 25 weeks
Oral capsule administered for up to 25 weeks
Topical cream administered for up to 25 weeks
Oral capsule administered for up to 25 weeks
Subcutaneous injection administered for up to 25 weeks
Subcutaneous injection administered for up to 25 weeks
Oral tablet administered for up to 25 weeks
Oral tablet administered for up to 25 weeks
Oral tablet administered for up to 25 weeks
Ancillary drug: Oral tablet administered as required
Ancillary drug: Oral tablet administered as required
Ancillary drug: Oral tablet administered as required
Ancillary drug: Oral tablet administered as required
Ancillary drug: Subcutaneous injection administered as required
Ancillary drug: Subcutaneous injection administered as required
Ancillary drug: Oral tablet administered as required
Ancillary drug: Oral tablet administered as required
Ancillary drug: Oral tablet administered as required
Ancillary drug: Oral tablet administered as required
Ancillary drug: Oral tablet administered as required
Ancillary drug: Oral tablet administered as required
Ancillary drug: Oral tablet administered as required
Ancillary drug: Oral tablet administered as required
Ancillary drug: Oral tablet administered as required
Ancillary drug: Oral tablet administered as required
Ancillary drug: Oral tablet administered as required
Ancillary drug: Oral tablet administered as required
Ancillary drug: Subcutaneous injection administered as required
Ancillary drug: Oral tablet administered as required
Ancillary drug: Oral tablet administered as required
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研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
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The incidence and severity of Treatment-related adverse events (TRAEs), including adverse events (AEs) and serious adverse events (SAEs), as assessed by the study physicians from baseline to 5.5 years after enrollment.
大体时间:Baseline to 5.5 years.
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Baseline to 5.5 years.
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The proportion of participants who discontinue PES due to TRAEs.
大体时间:Baseline to 5.5 years.
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Baseline to 5.5 years.
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Changes in sport-specific performance metrics, tailored to the athlete's discipline, in order to assess how individualized PES regimens translate into functional outcomes relevant to each sport (a)
大体时间:Baseline to week 27, followed by annual assessments until 5.5 years
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Delta in 100-meter track sprint time, 50-meter freestyle swim time, 100-meter freestyle swim time, 50-meter butterfly swim time, and 100-meter butterfly swim time, measured in seconds
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Baseline to week 27, followed by annual assessments until 5.5 years
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Changes in sport-specific performance metrics, tailored to the athlete's discipline, in order to assess how individualized PES regimens translate into functional outcomes relevant to each sport (b)
大体时间:Baseline to week 27, followed by annual assessments until 5.5 years
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Delta in snatch and clean & jerk (Olympic weightlifting total) measured in kilograms
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Baseline to week 27, followed by annual assessments until 5.5 years
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Impact of PES on respiratory function and aerobic capacity
大体时间:Baseline to week 27
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Change from baseline to week 27 in peak oxygen uptake (VO2 max) as measured by graded exercise test, reported in ml/kg/min.
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Baseline to week 27
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Impact of PES on blood and urine markers
大体时间:Baseline to 5.5 years.
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Number of participants with abnormal laboratory tests results. Measured from baseline through 5.5 years comprising up to 25 week PES exposure followed by a 5-year annual longitudinal follow-up. Markers include oxygen transport and immune system balance (CBC with 5-part differential); organ function and metabolic stress (comprehensive metabolic panel); iron status and oxygen-carrying capacity (serum iron, ferritin, transferrin saturation, TIBC); cardiovascular health and lipid metabolism (HDL, LDL, VLDL, triglycerides, Apo A1/B, lipoprotein(a)); hormonal balance and endocrine resilience (testosterone, estrogen, cortisol, DHEA, TSH, T3, T4, LH, FSH, prolactin); electrolyte and hydration balance (sodium, potassium, calcium, magnesium, chloride); systemic inflammation and immune activation (hs-CRP, ferritin, alpha-1 antitrypsin); and fatty acid profile and cellular membrane health (omega-3/omega-6 balance, EPA/DHA ratio, arachidonic acid). |
Baseline to 5.5 years.
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Impact of PES on cardiac structure and function (a)
大体时间:Baseline to week 27, followed by annual assessments until 5.5 years
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Change in left ventricular stroke volume (LV SV) assessed by echocardiogram.
Unit: mL/m²
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Baseline to week 27, followed by annual assessments until 5.5 years
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Impact of PES on cardiac structure and function (b)
大体时间:Baseline to week 27, followed by annual assessments until 5.5 years.
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Change in left ventricular ejection fraction (LVEF) and right ventricular fractional area change (RV FAC) assessed by echocardiagram. Unit: % |
Baseline to week 27, followed by annual assessments until 5.5 years.
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Impact of PES on cardiac structure and function (c)
大体时间:Baseline to week 27, followed by annual assessments until 5.5 years.
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Change in left ventricular stroke volume (LV SV) and right ventricular stroke volume (RV SV) assessed by CMR imaging. Unit: mL/m² |
Baseline to week 27, followed by annual assessments until 5.5 years.
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Impact of PES on cardiac structure and function (d)
大体时间:Baseline to week 27, followed by annual assessments until 5.5 years.
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Change in left ventricular ejection fraction (LVEF) and right ventricular ejection fraction (RVEF) assessed by CMR imaging. Unit: % |
Baseline to week 27, followed by annual assessments until 5.5 years.
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Impact of PES on cardiac structure and function (e)
大体时间:Baseline to week 27, followed by annual assessments until 5.5 years.
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Qualitative assessment of left and right ventricular myocardial fibrosis by location and extent using late gadolinium enhancement (LGE) on CMR imaging. Unit: Qualitative description (location and extent of fibrosis) |
Baseline to week 27, followed by annual assessments until 5.5 years.
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Impact of PES on cardiac structure and function (f)
大体时间:Baseline to week 27, followed by annual assessments until 5.5 years.
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Number of participants with abnormalities identified on resting 12-lead electrocardiography (ECG). Unit: Number of participants |
Baseline to week 27, followed by annual assessments until 5.5 years.
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Impact of PES on cardiac structure and function (g)
大体时间:Baseline to week 27, followed by annual assessments until 5.5 years.
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Number of participants with abnormalities identified during exercise stress ECG. Unit: Number of participants |
Baseline to week 27, followed by annual assessments until 5.5 years.
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Impact of PES on cardiac structure and function (h)
大体时间:Baseline to week 27, followed by annual assessments until 5.5 years.
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Number of participants with abnormalities identified during 24-hour ambulatory ECG monitoring. Unit: Number of participants |
Baseline to week 27, followed by annual assessments until 5.5 years.
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Impact of PES on cardiac structure and function (i)
大体时间:Baseline with repeat imaging over 5.5 years if clinically indicated.
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Coronary artery calcium score assessed by cardiac computed tomography (CT).
Unit: Agatston score (AU), categorised as 0, 1-10, 11-100, 101-400, >400
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Baseline with repeat imaging over 5.5 years if clinically indicated.
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Impact of PES on cardiac structure and function (j)
大体时间:Baseline with repeat imaging over 5.5 years if clinically indicated.
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Changes in participant qualitative description of coronary atherosclerosis assessed by cardiac computed tomography (CT). Unit: Delta in clinical abnormalities |
Baseline with repeat imaging over 5.5 years if clinically indicated.
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Impact of PES on neurological function (a)
大体时间:Baseline to week 27
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Change from baseline in cognitive memory performance (composite score of correct responses)
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Baseline to week 27
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Impact of PES on neurological function (b)
大体时间:Baseline to week 27
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Change from baseline in reaction time and processing speed.
Units: milliseconds
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Baseline to week 27
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Impact of PES on body composition (a)
大体时间:Baseline to week 27, followed by assessments at years 1, 3, and 5 years.
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Change from baseline in fat distribution.
Unit: % of total body weight
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Baseline to week 27, followed by assessments at years 1, 3, and 5 years.
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Impact of PES on body composition (b)
大体时间:Baseline to week 27, followed by assessments at years 1, 3, and 5 years.
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Change from baseline in bone mineral density at key sites (lumbar spine and hip).
Unit: Z-score
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Baseline to week 27, followed by assessments at years 1, 3, and 5 years.
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Impact of PES on body composition (c)
大体时间:Baseline to week 27, followed by assessments at years 1, 3, and 5 years.
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Change from baseline in landmark-based limb girth measurements (upper arm, thigh, calf) assessed by anthropometry. Unit: cm |
Baseline to week 27, followed by assessments at years 1, 3, and 5 years.
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Impact of PES on body composition (d)
大体时间:Baseline to week 27, followed by assessments at years 1, 3, and 5 years.
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Change from baseline in body water distribution, including extracellular water (ECW), intracellular water (ICW), and total body water (TBW). Unit: Litres (L) |
Baseline to week 27, followed by assessments at years 1, 3, and 5 years.
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Impact of PES on body composition (e)
大体时间:Baseline to week 27, followed by assessments at years 1, 3, and 5 years.
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Change from baseline in body mass index (BMI).
Unit: kg/m²
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Baseline to week 27, followed by assessments at years 1, 3, and 5 years.
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Impact of PES on musculoskeletal composition, function and strength (a)
大体时间:Baseline to week 27, followed by musculoskeletal composition imaging at years 1, 3, and 5 years.
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Change from baseline in cross-sectional area (CSA) of hip flexors and extensors assessed by MRI.
Unit: cm²
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Baseline to week 27, followed by musculoskeletal composition imaging at years 1, 3, and 5 years.
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Impact of PES on musculoskeletal composition, function and strength (b)
大体时间:Baseline to week 27, followed by musculoskeletal composition imaging at years 1, 3, and 5 years.
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Change from baseline in total muscle volume assessed by segmentation-based MRI analysis.
Unit: cm³
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Baseline to week 27, followed by musculoskeletal composition imaging at years 1, 3, and 5 years.
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Impact of PES on musculoskeletal composition, function and strength (c)
大体时间:Baseline to week 27, followed by musculoskeletal composition imaging at years 1, 3, and 5 years.
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Change from baseline in muscle thickness and shape assessed by MRI.
Unit: mm
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Baseline to week 27, followed by musculoskeletal composition imaging at years 1, 3, and 5 years.
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Impact of PES on musculoskeletal composition, function and strength (d)
大体时间:Baseline to week 27, followed by musculoskeletal composition imaging at years 1, 3, and 5 years.
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Change from baseline in grip strength.
Unit: Newtons
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Baseline to week 27, followed by musculoskeletal composition imaging at years 1, 3, and 5 years.
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Impact of PES on musculoskeletal composition, function and strength (e)
大体时间:Baseline to week 27, followed by musculoskeletal composition imaging at years 1, 3, and 5 years.
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Incidence of musculoskeletal injuries throughout study duration.
Unit: Number of events
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Baseline to week 27, followed by musculoskeletal composition imaging at years 1, 3, and 5 years.
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Abdominal, adrenal and thyroid health profiling
大体时间:Baseline to week 27, followed by ultrasound imaging at years 1, 3, and 5 years.
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Number of participants with abnormal clinical findings on abdominal, adrenal, and thyroid imaging (ultrasound), including abnormalities of organ size and structure (liver, kidneys, pancreas, spleen, gallbladder, bile ducts, adrenal glands, thyroid glands), tears, hernias, and pathological findings such as tumours, nodules, cysts, aneurysms, thrombosis, or inflammation. Unit: Number of participants |
Baseline to week 27, followed by ultrasound imaging at years 1, 3, and 5 years.
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其他结果措施
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Impact of PES on quality of life (QoL) (a)
大体时间:Baseline to week 27, followed by annual assessments up to 5.5 years.
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Change from baseline in score on the Generalized Anxiety Disorder 7-item scale (GAD-7), measuring severity of generalized anxiety. Scores range from 0 to 21, with higher scores indicating greater anxiety severity. Unit: Units on a scale |
Baseline to week 27, followed by annual assessments up to 5.5 years.
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Impact of PES on quality of life (QoL) (b)
大体时间:Baseline to week 27, followed by annual assessments up to 5.5 years.
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Change from baseline in score on the Patient Health Questionnaire 9-item scale (PHQ-9), measuring severity of depression. Scores range from 0 to 27, with higher scores indicating greater depression severity. Unit: Units on a scale |
Baseline to week 27, followed by annual assessments up to 5.5 years.
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Impact of PES on quality of life (QoL) (c)
大体时间:Baseline to week 27, followed by annual assessments up to 5.5 years.
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Change from baseline in score on the Athlete Burnout Questionnaire (ABQ). Scores range from 1 to 5, with higher scores indicating greater burnout. Unit: Units on a scale |
Baseline to week 27, followed by annual assessments up to 5.5 years.
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Impact of PES on quality of life (QoL) (d)
大体时间:Baseline to week 27, followed by annual assessments up to 5.5 years.
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Change from baseline in score on the PERMA Profiler, measuring well-being across five domains (positive emotion, engagement, relationships, meaning, and accomplishment). Scores range from 0 to 10, with higher scores indicating greater well-being. Unit: Units on a scale |
Baseline to week 27, followed by annual assessments up to 5.5 years.
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Impact of PES on quality of life (QoL) (e)
大体时间:Baseline to week 27, followed by annual assessments up to 5.5 years.
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Change from baseline in score on the Athlete Sleep Screening Questionnaire (ASSQ), measuring sleep habits and quality of sleep. Scores range from 0 to 17, with higher scores indicating greater sleep disturbance. Unit: Units on a scale |
Baseline to week 27, followed by annual assessments up to 5.5 years.
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Impact of PES on quality of life (QoL) (f)
大体时间:Baseline to week 27, followed by annual assessments up to 5.5 years.
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Change from baseline in score on the Hooper Questionnaire, measuring indicators of overtraining in athletes. Scores range from 4 to 28, with higher scores indicating greater overtraining burden. Unit: Units on a scale |
Baseline to week 27, followed by annual assessments up to 5.5 years.
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Impact of PES on quality of life (QoL) (g)
大体时间:Baseline to week 27, followed by annual assessments up to 5.5 years.
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Change from baseline in score on the Big Five TIPI measuring personality traits.
Scores range from 1 to 7 per domain, with higher scores indicating greater expression of each trait.
Unit: Units on a scale
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Baseline to week 27, followed by annual assessments up to 5.5 years.
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Impact of PES on quality of life (QoL) (h)
大体时间:Baseline to week 27, followed by annual assessments up to 5.5 years.
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Change from baseline in score on the HEXACO questionnaire, measuring personality traits.
Scores range from 1 to 5 per domain, with higher scores indicating greater expression of each trait.
Unit: Units on a scale
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Baseline to week 27, followed by annual assessments up to 5.5 years.
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Impact of PES on quality of life (QoL) (i)
大体时间:Baseline to week 27, followed by annual assessments up to 5.5 years.
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Change from baseline in score on the Sport Mental Health Assessment Tool 1 (SMHAT-1), an IOC mental health screening tool.
Scores range from 10 to 50, with higher scores indicating greater psychological distress.
Unit: Units on a scale
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Baseline to week 27, followed by annual assessments up to 5.5 years.
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Impact of PES on quality of life (QoL) (j)
大体时间:Baseline to week 27
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Change from baseline in score on the RT18 questionnaire, measuring risk-taking behaviour.
Scores range from 0 to 18, with higher scores indicating greater risk-taking propensity.
Unit: Units on a scale
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Baseline to week 27
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Impact of PES on quality of life (QoL) (k)
大体时间:Baseline to week 27
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Change from baseline in score on RISQ questionnaire, measuring risk-taking behaviours.
Scores range from 0 to 38, with higher scores indicating a greater number of endorsed risk behaviours.
Unit: Units on a scale
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Baseline to week 27
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Impact of PES on quality of life (QoL) (l)
大体时间:Baseline to week 27, followed by annual assessments up to 5.5 years.
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Change from baseline in score on the Total Quality of Recovery (TQR) scale, measuring perceived athlete recovery.
Scores range from 6 to 20, with higher scores indicating better perceived recovery.
Unit: Units on a scale
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Baseline to week 27, followed by annual assessments up to 5.5 years.
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Impact of PES on quality of life (QoL) (m)
大体时间:Week 27 to 6-month follow-up
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Change from week 27 in score on the Severity of Dependence Scale (SDS), measuring psychological dependence.
Scores range from 0 to 15, with higher scores indicating greater psychological dependence.
Unit: Units on a scale
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Week 27 to 6-month follow-up
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Impact of PES on physiological-lifestyle metrics (sleep, physical activity, stress levels and cardiovascular function) using continuous monitoring technologies (a)
大体时间:Baseline to week 27, followed by annual assessments up to 5.5 years.
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Change from baseline in sleep quality assessed by total sleep duration using Polar360 continuous monitoring technology.
Unit: Minutes per night
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Baseline to week 27, followed by annual assessments up to 5.5 years.
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Impact of PES on physiological-lifestyle metrics (sleep, physical activity, stress levels and cardiovascular function) using continuous monitoring technologies (b)
大体时间:Baseline to week 27, followed by annual assessments up to 5.5 years.
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Change from baseline in total daily energy expenditure using Polar360 continuous monitoring technology.
Unit: Kilocalories (kcal)
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Baseline to week 27, followed by annual assessments up to 5.5 years.
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Impact of PES on physiological-lifestyle metrics (sleep, physical activity, stress levels and cardiovascular function) using continuous monitoring technologies (c)
大体时间:Baseline to week 27, followed by annual assessments up to 5.5 years.
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Change from baseline in recovery score assessed by heart rate variability using Polar360 continuous monitoring technology.
Unit: Milliseconds (ms)
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Baseline to week 27, followed by annual assessments up to 5.5 years.
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Impact of PES on transcriptomic, proteomic and metabolomic biomarkers
大体时间:Baseline to week 27, followed by annual assessments up to 5.5 years.
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Number of participants with changes in the following laboratory tests results.
Markers measured include gene expression patterns (transcriptomics) associated with inflammation, metabolic regulation, and recovery status; circulating protein biomarkers (proteomics) linked to muscle remodeling, immune activation, hormonal signaling, known and novel biomarkers of exogenous PES use; change in metabolite profiles (metabolomics) involved in energy system utilization, oxidative stress, nutritional adaptation, and known and novel biomarkers of exogenous PES use
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Baseline to week 27, followed by annual assessments up to 5.5 years.
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Impact of PES on musculoskeletal function and tissue integrity (a)
大体时间:Baseline to week 27, followed by annual assessments up to 5.5 years.
|
Change from baseline in cardiorespiratory fitness assessed by maximal exercise test performance.
Unit: mL/kg/min (VO₂max)
|
Baseline to week 27, followed by annual assessments up to 5.5 years.
|
|
Impact of PES on musculoskeletal function and tissue integrity (b)
大体时间:Baseline to week 27, followed by annual assessments up to 5.5 years.
|
Change from baseline in force generation assessed by strength tests, including standing broad jump, standing overhead medicine ball throw, isometric mid-thigh pull, peak torque of quadriceps and hamstrings, hamstring-to-quadriceps strength ratio, and bilateral symmetry index.
Unit: Newtons (N)
|
Baseline to week 27, followed by annual assessments up to 5.5 years.
|
|
Impact of PES on musculoskeletal function and tissue integrity (c)
大体时间:Baseline to week 27, followed by annual assessments up to 5.5 years.
|
Number of participants with muscle-tendon architecture abnormal clinical values, assessed by ultrasound of Achilles and patellar tendons (morphology, tissue composition, structural integrity, elasticity, and mechanical properties) and skeletal muscle (muscle thickness, cross-sectional area, pennation angle, fascicle length, echo intensity, and Doppler vascularity).
Unit: Number of participants
|
Baseline to week 27, followed by annual assessments up to 5.5 years.
|
|
Effect of PES on hemoglobin mass
大体时间:Baseline to week 27, followed by annual assessments up to 5.5 years.
|
Change in total circulating hemoglobin mass based on carboxyhemoglobin (COHb) dilution and the CO inhaled from baseline to week 27.
|
Baseline to week 27, followed by annual assessments up to 5.5 years.
|
|
Impact of PES on lung function (a)
大体时间:Baseline to week 27, followed by annual assessments up to 5.5 years.
|
Change from baseline in pulmonary volumes assessed by spirometry, including forced vital capacity (FVC), forced expiratory volume in 1 second (FEV1), inspiratory vital capacity (IVC), slow vital capacity (SVC), expiratory reserve volume (ERV), and tidal volume (TV).
Unit: Litres (L)
|
Baseline to week 27, followed by annual assessments up to 5.5 years.
|
|
Impact of PES on lung function (b)
大体时间:Baseline to week 27, followed by annual assessments up to 5.5 years.
|
Change from baseline in FEV1/FVC ratio assessed by spirometry.
Unit: Ratio
|
Baseline to week 27, followed by annual assessments up to 5.5 years.
|
|
Impact of PES on lung function (c)
大体时间:Baseline to week 27, followed by annual assessments up to 5.5 years.
|
Change from baseline in airflow rates assessed by spirometry, including peak expiratory flow (PEF), forced expiratory flow at 25-75% of FVC (FEF25-75%), and maximal voluntary ventilation (MVV).
Unit: Litres per minute (L/min)
|
Baseline to week 27, followed by annual assessments up to 5.5 years.
|
合作者和调查者
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
- 荷尔蒙
- 激素、激素替代品和激素拮抗剂
- 肽激素
- 肽
- 氨基酸,肽和蛋白质
- 寡肽
- 蛋白质
- 硫化合物
- 有机化学品
- 杂环化合物,1形
- 杂环化合物
- 苯甲酰唑
- 杂环化合物,2环
- 杂环化合物,融合环
- 比尔
- 脂肪酸
- 脂质
- Azoles
- 碳氢化合物
- 碳氢化合物,循环
- 碳水化合物
- 生物碱
- 萘
- 多环芳烃
- 碳氢化合物,芳香族
- 多环化合物
- 咪唑
- 酰胺
- 苯胺化合物
- 胺
- 氨基酸
- 嘧啶
- 怀孕
- 类固醇
- 融合环化合物
- 苯衍生物
- 硝酸盐
- 酒精
- 碳氢化合物,卤素
- 杂环化合物,4个或更多环
- 吡咯
- 七酸
- 埃克森
- 埃斯特兰
- 雌二醇同源物
- 性腺类固醇激素
- 性腺激素
- 糖蛋白
- 糖缀合物
- 苯氧基丙酚胺
- 丙酚胺
- 氨基醇
- 丙醇
- 雄激素
- Androstanes
- 乙醇胺
- 怀孕
- 怀孕
- 氨基酸,芳香族
- 氨基酸,环状
- Biguanides
- 鸟齿
- 胺
- 磺酰胺
- 磺基酰胺
- 硫酮
- 苯佐皮人
- 菌落刺激因素
- 三轮唑
- Sti
- 苄基化合物
- 雄烯醇
- 睾丸激素同类物
- 氟苯烯
- 碳氢化合物,氟
- 四唑
- 垂体激素
- 麦角生物碱
- Ergolines
- 生长激素
- 垂体激素,前
- 苄氢化合物
- 双苯基化合物
- 甲状腺激素
- 叶黄素激素
- 孕酮同类物
- 甲状腺素
- 苯甲二嗪
- 噻嗪类
- 红细胞生成素
- 二肽
- 阿托伐他汀
- 瑞舒伐他汀钙
- 达贝泊汀阿尔法
- 奈必洛尔
- 阿那曲唑
- 替米沙坦
- 莫达非尼
- 卡麦角林
- 癸酸诺龙
- 二甲双胍
- 睾酮
- 呋塞米
- 美托洛尔
- 雌二醇
- 比索洛尔
- 黄体酮
- 普萘洛尔
- 洛沙坦
- 克罗米芬
- 依那普利
- 赖诺普利
- 阿得拉
- 诺龙
- Ortho Evra
- 氯噻嗪
- 睾丸激素17β-甲酸酯
- 人类生长激素
- 甲状腺素
- 丙酸睾丸激素
- 三甲基氨基氨酸
- 睾丸激素肠道
- 3-(2,2,2-三甲基肼)丙酸盐
- methenolone enanthate
- methenolone acetate
其他研究编号
- ASCEND001
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
在美国制造并从美国出口的产品
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