Aquatic power training dosing strategies and creatine in older adults
Official title: Optimization of Aquatic Power Training Dosing Strategies and the Effects of Creatine Supplementation on Functional and Multisystem Adaptations in Older Adults: A Randomized Controlled Trial
Run by University of Valencia · NCT07914270 · Data updated 2026-11-12
This trial tests whether different aquatic power training dosing methods and creatine supplementation help improve function in community-dwelling adults aged 60 and older.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 60 Years to 99 Years |
| Sex | All |
| Enrollment | 100 (estimated) |
| Sponsor | University of Valencia Academic / other |
| Locations | 1 site (Valencia, Valencia) |
| Status | Recruiting |
| Started | October 15, 2026 |
| Main results expected | April 30, 2027 |
| Study ends | May 15, 2027 |
| Registry record updated | November 3, 2026 |
| Trial ID | NCT07914270 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Community-dwelling adults aged 60 and older who are functionally independent and not currently in a structured high-intensity training program.
✕Probably not a fit
Individuals unable to participate safely in aquatic exercise or with unstable medical conditions may not benefit from this trial.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This randomized study assigns 5 groups of adults aged 60+ to compare two aquatic power training dosing strategies (RPE-1 guided vs. conventional time-based) with and without creatine, plus sedentary controls with and without creatine. Over 16 weeks, participants will train three 60-minute sessions per week or remain sedentary, to see how these approaches affect muscular power and multisystem health. The trial uses a double-factor design to isolate the effects of training dosage strategy and creatine supplementation on functional outcomes. Creatine is given as 3 g/day or placebo, and outcomes are measured after the intervention period. Lead by the University of Valencia with local collaborators, this study emphasizes community-dwelling older adults able to participate safely in aquatic exercise.
Why it matters
Potential benefit: If successful, the approach could optimize aquatic exercise programs and supplementation to support healthy aging and functional independence.
How similar studies have gone: Previous work shows potential benefits of aquatic power training and creatine in older adults, but this exact combination with randomized dosing strategies is novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Age ≥60 years at enrollment. 2. Community-dwelling and functionally independent in basic activities of daily living. 3. Able to ambulate independently, with or without usual assistive devices, and able to safely perform the physical assessments included in the study. 4. Clinically stable; participants with chronic diseases must have maintained stable pharmacological treatment for at least three months before the intervention. 5. Not currently participating in a structured moderate- or high-intensity strength or power training program or another systematic supervised exercise program. 6. Available and willing to participate throughout the 16-week intervention and complete all scheduled assessments. 7. Willing to accept random allocation to any study group and creatine or placebo supplementation when applicable. 8. Willing to maintain stable dietary habits throughout the intervention. 9. Able and willing to provide written informed consent Exclusion Criteria: 1. Uncontrolled cardiovascular, respiratory, metabolic, neurological, or musculoskeletal disease contraindicating exercise or limiting safe participation. 2. Unfavorable medical assessment for participation in supervised exercise. 3. Uncontrolled hypertension at screening. 4. Known kidney disease, renal failure, or clinically relevant impairment of renal function. 5. Active liver disease or clinically relevant impairment of liver function. 6. Active malignant neoplasm or current cancer treatment. 7. Endocrine or metabolic disorders considered by the research team to substantially interfere with the study's primary outcomes. 8. Current use, or use during the previous three months, of creatine or other supplements with potential ergogenic or anabolic effects. 9. Pharmacological treatment considered likely to substantially modify the study's primary outcomes. 10. Participation during the previous three months in a systematic moderate- or high-intensity strength or power training program.
Where it's running
-
Physical activity and Sport Science Faculty
Valencia, Valencia, Spain Recruiting
Study contacts
- Study coordinator: Juan Carlos Colado Sánchez, Chair full professor
- Email: juan.colado@uv.es
- Phone: (9639) 83470
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.