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Impact of Medically Supervised Performance-Enhancing Substances (PES) on Elite Athletes (ASCEND001)

2026年4月28日 更新者:Enhanced Emirates Limited

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

详细说明

This study employs a prospective hybrid design comprising an observational cohort alongside a non-randomised interventional cohort, allowing for individualized PES regimens, biomarker-informed adaptation, and alignment with each athlete's training cycle while providing for the first time prospective data on safety parameters and performance effects of PES. It emphasizes within-subject change over time rather than between-group comparisons, offering a more ecologically valid framework for observing enhancement in context. Participants will continue periodized training while under continuous monitoring, enabling assessment of both physiological response and performance progression under real-world conditions. Similar study designs that aim to determine optimal therapy customization to individuals with specific biomarkers are becoming increasingly popular in precision medicine.

研究类型

介入性

注册 (估计的)

60

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

是的

描述

Inclusion Criteria:

Participants are eligible to be included in the study only if all the following criteria apply:

  1. Participant must be 18 years of age or older at the time of signing the informed consent.
  2. Capable of giving signed informed consent, which includes compliance with the requirements and restrictions listed in the ICF and in this protocol.
  3. 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.
  4. Participant must be under the care of a primary care provider (PCP).
  5. Participant passes medical profiling assessment (measuring overall state of health and quality of life)
  6. Females must meet one of the following:

    1. Postmenopausal (>45 years of age with amenorrhea for at least 12 months, without using exogenous hormonal contraception and with FSH ≥ 40 IU/L).
    2. Surgically sterile (hysterectomy, bilateral salpingectomy; oophorectomy) for at least 6 months.
    3. 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:

  1. 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:

    1. 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.
    2. A history of severe mental health conditions (e.g., schizophrenia, bipolar disorder) that have required intensive intervention or hospitalization within the past 5 years.
  2. 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.
  3. Has a history of CV disease that includes any of the following:

    1. Unstable CV disease, myocardial infarction, unstable angina, cardiac bypass or coronary arteries stenting, cerebrovascular accident (stroke), or transient ischemic attack.
    2. 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.

    3. 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.
  4. Current or history of clinically significant (per Investigator's judgment) liver or biliary disease.
  5. Current acute or chronic self-reported HCV and/or HBV infection.
  6. Current or history of clinically significant renal disease (per Investigator's judgment) or GFR <60mL/min/1.73m2
  7. 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.
  8. 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.

  9. Pregnant or breastfeeding.
  10. Has a mental or legal incapacity.
  11. 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

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

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
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.
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.
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

研究衡量的是什么?

主要结果指标

结果测量
大体时间
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.
Baseline to 5.5 years.
The proportion of participants who discontinue PES due to TRAEs.
大体时间:Baseline to 5.5 years.
Baseline to 5.5 years.

次要结果测量

结果测量
措施说明
大体时间
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
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
Baseline to week 27, followed by annual assessments until 5.5 years
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
Delta in snatch and clean & jerk (Olympic weightlifting total) measured in kilograms
Baseline to week 27, followed by annual assessments until 5.5 years
Impact of PES on respiratory function and aerobic capacity
大体时间:Baseline to week 27
Change from baseline to week 27 in peak oxygen uptake (VO2 max) as measured by graded exercise test, reported in ml/kg/min.
Baseline to week 27
Impact of PES on blood and urine markers
大体时间:Baseline to 5.5 years.

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.
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
Change in left ventricular stroke volume (LV SV) assessed by echocardiogram. Unit: mL/m²
Baseline to week 27, followed by annual assessments until 5.5 years
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.

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.
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.

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.
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.

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.
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.

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.
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.

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.
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.

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.
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.

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.
Impact of PES on cardiac structure and function (i)
大体时间:Baseline with repeat imaging over 5.5 years if clinically indicated.
Coronary artery calcium score assessed by cardiac computed tomography (CT). Unit: Agatston score (AU), categorised as 0, 1-10, 11-100, 101-400, >400
Baseline with repeat imaging over 5.5 years if clinically indicated.
Impact of PES on cardiac structure and function (j)
大体时间:Baseline with repeat imaging over 5.5 years if clinically indicated.

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.
Impact of PES on neurological function (a)
大体时间:Baseline to week 27
Change from baseline in cognitive memory performance (composite score of correct responses)
Baseline to week 27
Impact of PES on neurological function (b)
大体时间:Baseline to week 27
Change from baseline in reaction time and processing speed. Units: milliseconds
Baseline to week 27
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.
Change from baseline in fat distribution. Unit: % of total body weight
Baseline to week 27, followed by assessments at years 1, 3, and 5 years.
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.
Change from baseline in bone mineral density at key sites (lumbar spine and hip). Unit: Z-score
Baseline to week 27, followed by assessments at years 1, 3, and 5 years.
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.

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.
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.

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.
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.
Change from baseline in body mass index (BMI). Unit: kg/m²
Baseline to week 27, followed by assessments at years 1, 3, and 5 years.
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.
Change from baseline in cross-sectional area (CSA) of hip flexors and extensors assessed by MRI. Unit: cm²
Baseline to week 27, followed by musculoskeletal composition imaging at years 1, 3, and 5 years.
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.
Change from baseline in total muscle volume assessed by segmentation-based MRI analysis. Unit: cm³
Baseline to week 27, followed by musculoskeletal composition imaging at years 1, 3, and 5 years.
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.
Change from baseline in muscle thickness and shape assessed by MRI. Unit: mm
Baseline to week 27, followed by musculoskeletal composition imaging at years 1, 3, and 5 years.
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.
Change from baseline in grip strength. Unit: Newtons
Baseline to week 27, followed by musculoskeletal composition imaging at years 1, 3, and 5 years.
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.
Incidence of musculoskeletal injuries throughout study duration. Unit: Number of events
Baseline to week 27, followed by musculoskeletal composition imaging at years 1, 3, and 5 years.
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.

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.

其他结果措施

结果测量
措施说明
大体时间
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.

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.
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.

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.
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.

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.
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.

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.
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.

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.
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.

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.
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.
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
Baseline to week 27, followed by annual assessments up to 5.5 years.
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.
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
Baseline to week 27, followed by annual assessments up to 5.5 years.
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.
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
Baseline to week 27, followed by annual assessments up to 5.5 years.
Impact of PES on quality of life (QoL) (j)
大体时间:Baseline to week 27
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
Baseline to week 27
Impact of PES on quality of life (QoL) (k)
大体时间:Baseline to week 27
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
Baseline to week 27
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.
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
Baseline to week 27, followed by annual assessments up to 5.5 years.
Impact of PES on quality of life (QoL) (m)
大体时间:Week 27 to 6-month follow-up
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
Week 27 to 6-month follow-up
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.
Change from baseline in sleep quality assessed by total sleep duration using Polar360 continuous monitoring technology. Unit: Minutes per night
Baseline to week 27, followed by annual assessments up to 5.5 years.
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.
Change from baseline in total daily energy expenditure using Polar360 continuous monitoring technology. Unit: Kilocalories (kcal)
Baseline to week 27, followed by annual assessments up to 5.5 years.
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.
Change from baseline in recovery score assessed by heart rate variability using Polar360 continuous monitoring technology. Unit: Milliseconds (ms)
Baseline to week 27, followed by annual assessments up to 5.5 years.
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.
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
Baseline to week 27, followed by annual assessments up to 5.5 years.
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

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2026年3月12日

初级完成 (估计的)

2028年5月1日

研究完成 (估计的)

2033年3月1日

研究注册日期

首次提交

2026年4月17日

首先提交符合 QC 标准的

2026年4月28日

首次发布 (实际的)

2026年5月6日

研究记录更新

最后更新发布 (实际的)

2026年5月6日

上次提交的符合 QC 标准的更新

2026年4月28日

最后验证

2026年4月1日

更多信息

与本研究相关的术语

其他相关的 MeSH 术语

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)?

未定

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

在美国制造并从美国出口的产品

是的

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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