- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06449456
Exercise Capacity, Physical Fitness, and Physical Activity Levels in Children With CAH
A Comparison of Exercise Capacity, Muscle Functions, Physical Fitness, and Physical Activity Levels in Children With Congenital Adrenal Hyperplasia and Healthy Controls
Study Overview
Status
Detailed Description
Congenital adrenal hyperplasia (CAH) is a group of autosomal recessive diseases caused by the deficiency of one of the five enzymes necessary for cortisol synthesis in the adrenal cortex. Dysfunction in cortisol synthesis, as seen in other enzyme deficiencies, leads to an increase in adrenocorticotropic hormone (ACTH) secretion, resulting in hypertension and hypokalemia. Additionally, patients with CAH exhibit excess androgens alongside cortisol deficiency. İn CAH treatment, glucocorticoids are used to suppress androgen production in the adrenal cortex. Deficiency in glucocorticoids and mineralocorticoids, as well as excess androgens, can contribute to the development of adverse metabolic and cardiovascular anomalies.
Ongoing research has revealed a predisposition for adverse metabolic changes in children and adolescents with CAH, including obesity, hypertension, insulin resistance, and increased intima-media thickness, which can increase the risk of developing cardiovascular disease in adulthood. Furthermore, subclinical left ventricular diastolic dysfunction has been observed in adolescents with CAH. İn these patients, due to the deficiency of epinephrine there is an increased tendency for hypoglycemia under stress conditions.
These metabolic changes can lead to impaired exercise performance in patients with CAH, consequently affecting their quality of life.
A study involving twenty classic CAH adolescents and twenty healthy counterparts demonstrated that classic CAH patients exhibited reduced exercise capacity with lower peak workload and higher peak systolic blood pressure during exercise. However, there is a lack of research in the literature comparing respiratory and peripheral muscle strength, daily life activities, physical fitness, and levels of physical activity in children and adolescents with CAH to their healthy peers.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
State
-
Ankara, State, Turkey, 06100
- Hacettepe University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria for CAH Group:
- Diagnosed with Congenital Adrenal Hyperplasia
- Aged between 8-18 years
- Providing voluntary consent from both themselves and their parents
- Able to cooperate
Exclusion Criteria for CAH Groups:
- Having any systemic disease that may affect the measurement parameters
Inclusion Criteria for Healthy Group:
- Not having any chronic diseases
- Aged between 8-18 years
- Willing to participate in the study
- Able to cooperate
Exclusion Criteria for Healthy Group:
- Not willing to participate in the study
- Presence of cooperation and communication problems
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
|
Patients with Congenital Adrenal Hyperplasia
Patients between the ages of 8-18 years who have been diagnosed with Congenital Adrenal Hyperplasia
|
|
Healthy Controls
Age and sex matched healthy controls between the ages of 8-18 years
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Respiratory Muscle Strength
Time Frame: 1 day
|
Respiratory muscle strength will be measured using a portable, electronic mouth pressure measurement device (Micro Medical MicroMPM, UK).
The best of three measurements for Maximal inspiratory pressure (MIP) and Maximal expiratory pressure (MEP) will be selected.
Real MIP and MEP values and the percentages of expected values based on age and gender will be used in the analyses.
|
1 day
|
|
Peripheral Muscle Strength
Time Frame: 1 day
|
Peripheral muscles'strength will be assessed using the K-Force hand dynamometer.
|
1 day
|
|
Physical Fitness Level
Time Frame: 1 day
|
It will be evaluated with the Fitnessgram test battery.
|
1 day
|
|
Functional Exercise Capacity
Time Frame: 1 day
|
It will be measured using the 6-Minute Walk Test.
|
1 day
|
|
Handgrip strength
Time Frame: 1 day
|
Jamar hand dynamometer (Jamar®, California, USA) will be used to measure grip strength.
|
1 day
|
|
Physical Activity Level
Time Frame: 1 day
|
The Physical Activity Level will be assessed using the Physical Activity Questionnaire for Adolescents (PAQ-A) and the Physical Activity Questionnaire for Children (PAQ-C).
The scores for PAQ-A and PAQ-C range from 9 to 45, with higher scores indicating better physical activity levels.
The results of both questionnaires will be presented separately.
The PAQ-A score will be reported as a distinct outcome measure for adolescents, and the PAQ-C score will be reported as a distinct Outcome Measure for children.
This approach ensures a clear evaluation of physical activity levels in both age groups.
|
1 day
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Anthropometric Measurements
Time Frame: 1 day
|
Anthropometric measurements will include separate measurements of waist and hip circumference, and calculations of the waist/hip ratio and waist/height ratio.
|
1 day
|
|
Participation
Time Frame: 1 day
|
Quality of life will be assessed using the Pediatric Outcome Data Collection Instrument (PODCI) child and adolescent form.
Scores for all dimensions range from 0 to 100, with 100 indicating the highest level of function or participation.
|
1 day
|
|
Heart Rate Variability
Time Frame: 1 day
|
HRV will be assessed by measuring it with the Polar H10 device before, after, and during the recovery phase of the 6-minute walk test, specifically in the first and second minutes.
|
1 day
|
|
Body composition
Time Frame: 1 day
|
Body composition will be evaluated using bioelectric impedance analysis (Body Composition Analyzer MC-780MA).
Measurements will include fat mass, fat-free mass, and water percentage.
Each of these measurements will be reported as separate outcome measures.
Fat mass will be reported in kilograms, fat-free mass in kilograms, and water percentage as a percentage of total body weight.
|
1 day
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Ebru CALIK KUTUKCU, PhD, Ankara, Hacettepe University, Türkiye, 06100 Contact: Phd 0903123051576 Ext.195 ecalik85@gmail.com
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Urogenital Diseases
- Endocrine System Diseases
- Pathologic Processes
- Male Urogenital Diseases
- Female Urogenital Diseases
- Female Urogenital Diseases and Pregnancy Complications
- Metabolism, Inborn Errors
- Genetic Diseases, Inborn
- Metabolic Diseases
- Gonadal Disorders
- Congenital Abnormalities
- Adrenal Gland Diseases
- Disorders of Sex Development
- Urogenital Abnormalities
- Steroid Metabolism, Inborn Errors
- Hyperplasia
- Adrenal Hyperplasia, Congenital
- Adrenogenital Syndrome
Other Study ID Numbers
- SBA 24/096
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Quality of Life
-
Ziekenhuis Oost-LimburgRecruitingQuality of Life | Postoperative Quality of Recovery | Health-Related Quality-of-LifeBelgium
-
B. Braun Medical SAUnknownQuality of Life of Colostomized Patient
-
Assiut UniversityUnknownImproving Quality of LifeEgypt
-
Istituto Ortopedico RizzoliUniversity of BolognaCompletedImprove Quality of LifeItaly
-
Children's National Research InstituteCompletedProfessional Quality of LifeUnited States
-
Region VästmanlandUnknownHealth Related Quality of Life
-
Ain Shams UniversityCompletedHealth Related Quality of LifeEgypt
-
Institute of Oncology LjubljanaUnknownHealth-related Quality of LifeSlovenia
-
Oslo University HospitalNorwegian Fund for Postgraduate Training in PhysiotherapyCompletedHealth-Related Quality of LifeNorway
-
Mattu UniversityCompletedBreif Description: Patients' Quality of Life ofEthiopia