NCT07156708 Aquatic Exercises Combined With Cognitive Tasks for Older Adults
| NCT ID | NCT07156708 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Federal University of Pelotas |
| Condition | Aging |
| Study Type | INTERVENTIONAL |
| Enrollment | 98 participants |
| Start Date | 2025-09-05 |
| Primary Completion | 2027-08 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 98 participants in total. It began in 2025-09-05 with a primary completion date of 2027-08.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The aquatic environment has characteristics that favor the adherence of older adults to exercise programs, and studies have shown that programs in this setting are effective in enhancing various aspects of physical fitness as well as cognitive function in this population. Research has explored whether incorporating cognitive tasks into an aquatic exercise program could offer additional benefits, but it remains uncertain whether this approach leads to greater improvements in cognitive function compared to aquatic exercises alone. The present protocol reports the WaterCog Study, which aims to evaluate the effects of an aquatic aerobic exercise program combined with cognitive tasks, compared to a conventional aquatic aerobic exercise program and a control group, on cognitive function and other health-related outcomes in older adults. This trial is a randomized, single-blinded, three-arm, parallel, superiority trial. A total of 98 older adults are randomized into one of three groups: 1) an aquatic aerobic exercise program combined with cognitive tasks, 2) a conventional aquatic aerobic exercise program, and 3) a control group. Participants in both exercise groups complete a 12-week exercise program with two weekly sessions on non-consecutive days. The primary outcome is cognitive function, while secondary outcomes include physical function, cardiovascular, and psychosocial parameters. Outcomes are measured at baseline, post-intervention, and at the 12-week follow-up after the end of the intervention period. The analysis plan will employ an intention-to-treat approach and per-protocol criteria. The conceptual hypothesis of the study is that both training programs will significantly improve the investigated outcomes compared to the control group. Additionally, it is expected that aquatic exercises with cognitive tasks will promote additional benefits in cognitive function, with similar gains in physical function, cardiovascular, and psychosocial parameters compared to conventional aquatic aerobic exercises in post-intervention and follow-up measures.
Eligibility Criteria
Inclusion Criteria: * Older women aged 60 and 75 years; * Being physically inactive, meaning not participating in physical exercise for at least six months (regular exercise is defined as engaging in any physical training for a minimum of 20 minutes on two or more days a week). Exclusion Criteria: * History of cardiovascular disease (except controlled hypertension); * Osteoarticular limitations for the practice of exercises; * Being illiterate due to the self-completion questionnaires and the characteristics of the intervention; * Diagnosis of dementia, schizophrenia, or major depressive disorder.
Contact & Investigator
Cristine L Alberton, PhD
PRINCIPAL INVESTIGATOR
Federal University of Pelotas
Frequently Asked Questions
Who can join the NCT07156708 clinical trial?
This trial is open to female participants only, aged 60 Years or older, up to 75 Years, studying Aging. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07156708 currently recruiting?
Yes, NCT07156708 is actively recruiting participants. Contact the research team at marianaaaborba@gmail.com for enrollment information.
Where is the NCT07156708 trial being conducted?
This trial is being conducted at Pelotas, Brazil.
Who is sponsoring the NCT07156708 clinical trial?
NCT07156708 is sponsored by Federal University of Pelotas. The principal investigator is Cristine L Alberton, PhD at Federal University of Pelotas. The trial plans to enroll 98 participants.