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Clinical Trials in Turkey / NCT07575958
Active, not recruiting Not applicable

Effects of Aquatic Exercise in Older Adults With Sarcopenia:A Randomized Trial

NCT07575958 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-05-01
Last updated
2026-09-25

Condition(s) studied

SarcopeniaSarcopenia in Elderly

Investigational drug(s) / intervention(s)

Aquatic Exercise ProgramHome Exercise Program

Aquatic Exercise Program: The aquatic exercise program will be conducted under supervision in a pool environment for a total of 15 sessions over 6 weeks. The program will consist of 2 sessions per week during the first 3 weeks and 3 sessions per week during the last 3 weeks. Each session will include structured exercises designed to improve muscle strength, balance, and functional performance in older adults with sarcopenia. Participants will also continue a standardized home exercise program throughout the study period.

Home Exercise Program: Participants in the control group will perform a standardized home exercise program for a total of 6 weeks. The program will consist of exercises designed to improve muscle strength, balance, and functional performance in older adults with sarcopenia. Participants will be instructed to perform the exercises regularly at home throughout the study period. No supervised aquatic exercise or additional intervention will be provided.

Study summary

Sarcopenia is a geriatric syndrome characterized by age-related loss of skeletal muscle mass, strength, and physical performance, leading to increased risk of falls, functional decline, and reduced quality of life. Exercise interventions, particularly resistance training, are effective in managing sarcopenia; however, land-based exercises may be challenging for older adults due to balance impairments, joint problems, and fear of falling.

Pool-based exercise programs may offer a safe and feasible alternative, as water buoyancy reduces joint loading while providing resistance to support muscle strengthening. Despite these potential benefits, evidence regarding the effects of aquatic exercise in individuals with sarcopenia remains limited, especially in Türkiye.

This study aims to evaluate the effects of a 6-week supervised pool-based exercise program on muscle strength, muscle morphology, physical performance, mood, and quality of life in individuals aged 65 years and older with sarcopenia. Sarcopenia will be identified using the Sonographic Thigh Adjustment Ratio (STAR), based on ultrasound measurements of anterior thigh muscle thickness. In addition, appendicular skeletal muscle mass will be assessed using bioelectrical impedance analysis (ASM/height²).

Outcome measures will include ultrasound-based muscle thickness, STAR, muscle strength, functional performance tests, depressive symptoms, and health-related quality of life. Assessments will be performed at baseline, immediately after the intervention, and at 1-month follow-up.

Eligibility

Sex
ALL
Min age
65 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Age ≥65 years 2. Diagnosis of "definite sarcopenia" according to the ISarcoPRM diagnostic algorithm 3. Not receiving nutritional supplementation and not requiring nutritional support according to the Mini Nutritional Assessment (MNA) 4. Sufficient cognitive ability to understand and follow instructions, including study-related questions and the home exercise program 5. Voluntary participation in the study 6. Ability to ambulate independently (assistive devices such as a cane are allowed; however, fully dependent individuals will be excluded) Exclusion Criteria: 1. Inability to complete assessment tests and questionnaires 2. Presence of severe systemic disease that may contraindicate exercise 3. Severe visual or hearing impairment 4. Presence of a cardiac pacemaker 5. Severe cardiopulmonary disease 6. Uncontrolled hypertension 7. Uncontrolled diabetes mellitus 8. Receiving nutritional supplementation 9. Severe anemia 10. Conditions contraindicating hydrotherapy, including aquaphobia (fear of water), behavioral disorders, dyspnea at rest, urinary or fecal incontinence, known chlorine allergy, open wounds, acute systemic illness, epilepsy, tracheostomy, indwelling drainage devices, and immunodeficiency

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Gaziosmanpasa Research and Education Hospital Istanbul Istanbul
University of Health Sciences Gaziosmanpaşa Training and Research Hospital Istanbul Istanbul

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07575958 on ClinicalTrials.gov ↗ ← All trials in Turkey