AgingWaterCogNCT07156708
Aquatic Exercises Combined With Cognitive Tasks for Older Adults
A study testing Aquatic aerobic exercise program and Cognitive tasks in people with Aging, run by Federal University of Pelotas at 1 site in Brazil.
Trial 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. Read more about this study
- Who is it for?
- Ages 60 to 75 years, women onlyHealthy volunteers can take part
- Conditions the study is for
- Aging
- What is being tested?
- Aquatic aerobic exercise program and Cognitive tasks
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 98 participants
- Where
- 1 siteBrazil
- Study dates
- 5 Sep 2025to Aug 2027
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 60 to 75 years
- Women only
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- 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).
Who cannot join
- 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.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Brazil1 site, 1 recruiting
- Recruiting
Escola Superior de Educação Física e Fisioterapia
Pelotas, Rio Grande do Sul, 96055-630
Cristine L Alberton, PhD, 5551984062864, tinialberton@yahoo.com.br
About this study
Official title: Effects of Aquatic Aerobic Exercises Combined With Cognitive Tasks on Cognitive Function and Other Health-related Outcomes in Older Adults
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.
- Conditions
- Aging
- Being tested
- Aquatic aerobic exercise program, Cognitive tasks
- Keywords
- Physical exercise, Physical activity, Dual-task training, Water-based exercise, Cognitive function, Physical fitness, Mental health, Sleep quality, Quality of life, Cardiovascular parameters
- Medical subject headings
- Motor Activity, Psychological Well-Being, Sleep Initiation and Maintenance Disorders
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Aquatic aerobic exercise programOther
The aquatic exercise sessions include the following exercises: butt kick, frontal kick, cross-country skiing, and stationary running. These exercises are commonly used in water aerobics classes and provide controlled osteoarticular impact, being safe for older women (Alberton et al., 2019). Training intensity is prescribed using Borg's 6-20 rating of perceived exertion (RPE) scale. The adopted strategy is based on interval training, which alternates between high-intensity effort and low-intensity active recovery phases. Each block consists of 4 minutes of effort (RPE 13 - 15), with one minute for each exercise (butt kick, frontal kick, cross-country skiing, and stationary running) followed by 1 minute of active recovery (RPE 11), performed with stationary running. To facilitate monitoring, an RPE scale (measuring 0.90 × 1.20 m) is fixed to the outside of the pool, in front of the participants.
Cognitive tasksOther
This group performs the same aerobic training protocol used by the conventional aquatic program group. Additionally, cognitive tasks are performed during the active recovery phases. Cognitive training encompasses different domains of cognition in all sessions, including semantic fluency, processing speed, cognitive flexibility, inhibitory control, memory, attention, and reasoning. The exercises vary in each class, with progression in complexity in each mesocycle.
| Study group | Role | What they receive |
|---|---|---|
| Aquatic aerobic exercise program combined with cognitive tasks | Experimental | Not described Receives: Other: Aquatic aerobic exercise program; Other: Cognitive tasks |
| Conventional aquatic aerobic exercise program | Experimental | Not described Receives: Other: Aquatic aerobic exercise program |
| Control group | No intervention | Not described |
What is being measured
The primary outcome is the main question the study is designed to answer.
Objective cognitive function - Digit Span Test
The Digit Span Test is used to assess working memory and attention span (Schroeder et al., 2012). The Digit Span Test requires participants to verbally recall a sequence of numbers dictated by the examiner. The test begins with three numbers ranging from 0 to 9, read at 1-second intervals, which participants must remember in the correct order. The sequence increases by one digit if pronounced correctly. If participants fail to recall the correct sequence twice in a row, the test ends. The number of digits correctly recalled is recorded as the test result, with a higher score indicating better performance.
Measured: Baseline (week 0), post-intervention (week 13), and 12-week follow-up (week 25)
Objective cognitive function - Controlled Oral Word Association Test
The Controlled Oral Word Association Test (COWAT) is used to assess verbal fluency, working memory, and inhibitory control (Ross et al., 2007). In this test, participants must say as many words as possible that start with the letters "F," "A," and "S" within 1 minute for each letter. Proper names, repeated words, and variations in gender, number, and conjugation are not considered. A higher number of words in each test indicates better verbal fluency.
Measured: Baseline (week 0), post-intervention (week 13), and 12-week follow-up (week 25)
Secondary outcomes (14)
Objective cognitive function - Trail Making Test (TMT)
The validated version of the Trail Making Test (TMT) for the Brazilian population is used to assess aspects of objective cognitive function (Carvalho \& Caramelli, 2020). In the first part of the instrument (TMT-A), which measures visual attention and processing speed, participants must draw a line connecting the numbers 1 to 25 in ascending order. In the second part (TMT-B), which measures cognitive flexibility and executive function, participants connect numbers (1-13) and letters (A-L) in an interleaved numerical and alphabetical order. Participants are instructed to maintain pencil-and-paper contact throughout the test, and shorter completion times indicate better performance.
Measured: Baseline (week 0), post-intervention (week 13), and 12-week follow-up (week 25)
Self-perception of cognitive function
The Brazilian version of the Cognitive Failures Questionnaire (CFQ) is used to measure the frequency of cognitive failures in everyday life, such as lapses in attention, memory problems, and failures in executing intentional actions (Paula et al., 2017). The questionnaire consists of 25 self-administered items, with responses on a Likert-type scale from 0 to 4, which assess the frequency of cognitive failures in different everyday contexts. The total score ranges from 0 to 100 points, with higher scores indicating a greater perceived frequency of cognitive failures and, therefore, poorer self-perception of cognitive function.
Measured: Baseline (week 0), post-intervention (week 13), and 12-week follow-up (week 25)
Aerobic fitness
The 6-minute Walk Test (6MWT) is performed to measure aerobic fitness. The course proposed in the original test is 45.72 m rectangular. The course will be adapted for a straight line of 30 m in length, demarcated with cones every 3 m. Participants are instructed to walk for 6 minutes in a flat 30m course, where the total distance walked "as fast as possible" is assessed
Measured: Baseline (week 0) to post-training (week 13)
Lower limb strength
The 30-s Chair-Stand test is performed to measure the strength of the lower limbs. Participants are instructed to sit and stand up from a chair 43 cm high from the seat, without the aid of the upper limbs, as many times as possible for 30 s. The total number of complete repetitions performed within the 30 seconds is recorded as the result, with higher values indicating greater lower body strength.
Measured: Baseline (week 0) to post-training (week 13)
Upper limb strength
The Arm Curl test is performed to measure the strength of the upper limbs. Starting at full elbow extension and holding a 2 kg dumbbell in each hand, participants are instructed to perform the maximal number of elbow crunches over the full range of motion for 30 s. The test is performed with both upper limbs. The total number of complete repetitions performed within the 30 s is recorded as the result, with higher values indicating greater upper body strength.
Measured: Baseline (week 0) to post-training (week 13)
Lower limb flexibility
The Sit-and-Reach test is performed using a Wells Bench to assess lower limb flexibility, particularly of the hamstring and lower back muscles. Participants sit barefoot on the floor with their legs extended and together, knees fully extended, and the soles of the feet flat against the front of the bench. With arms extended and hands overlapping, they slowly bend forward from the hips, sliding their hands along the measurement scale on the bench, without flexing the knees or using compensatory movements. The maximum reach is held for approximately two seconds, and the greatest distance reached in centimeters in three attempts is recorded.
Measured: Baseline (week 0) to post-training (week 13)
Agility and dynamic balance
The Timed Up and Go (TUG) test is performed to measure agility and dynamic balance. Participants are instructed to get up from the chair (43 cm), turn around a marker that will be 3m, and return to the starting position. The shortest time of the two attempts is considered the result.
Measured: Baseline (week 0) to post-training (week 13)
Dual-task performance
Dual-task performance involves simultaneously performing the TUG test and a cognitive task. Participants are instructed to do the TUG while reciting alternating letters (e.g., A, C, E, etc.). The time taken for the TUG and the number of correctly recited letters are recorded as test results.
Measured: Baseline (week 0) to post-training (week 13)
Blood pressure
Office systolic blood pressure (SBP) and diastolic blood pressure (DBP) measurements are obtained using calibrated and automated oscillometric devices (HEM-7320, OMRON, China). Participants are kept in a calm environment for 5 min, and then measurements are performed in both arms of the participant. Three measurements, with an interval of 1 to 2 min, are taken in the arm with the highest initial value. The average of the three measurements is considered the subject's office blood pressure.
Measured: Baseline (week 0) to post-training (week 13)
Blood pressure reactivity
Blood pressure reactivity is measured as the difference between values recorded during a mental stressor and those obtained at rest. The Stroop Test (Stroop, 1935) is used to induce mental stress, presented via a video on a screen in front of the participant for three minutes. Every two seconds, a visual stimulus consisting of a word written in a specific color will appear, with the color of the word and its meaning being incongruent (for example, the word "blue" written in red). The participant must respond verbally and as quickly as possible to the color of the letters, ignoring the meaning of the word.
Throughout the test, systolic and diastolic blood pressure are measured by the auscultatory method, using a stethoscope and a calibrated aneroid sphygmomanometer, with one reading every minute, for a total of three readings. The reference arm is the same one used for resting BP assessments. After completing the test, participants are asked to rate their perceived stress level using a
Measured: Baseline (week 0) to post-training (week 13)
Heart rate variability
Heart rate variability (HRV) is measured with participants seated and resting for 10 minutes, during which time their heart rate is continuously recorded using the Polar H10 chest sensor, a validated and widely used device for HRV analysis. Data collection takes place in a quiet environment, with a controlled temperature between 24°C and 26°C. Data is collected via Bluetooth and stored in the Polar Flow app, later exported in a compatible format (.txt or .csv). The final five minutes of the resting period are considered for analysis, as they offer greater physiological stability. Data are processed in Kubios HRV® software, with automatic artifact correction using a low threshold filter. HRV analysis follows the recommendations of the Task Force of the European Society of Cardiology and the North American Society of Pacing and Electrophysiology (1996), considering time-domain parameters such as SDNN (Standard Deviation of NN Intervals), which reflects the global variability of autonomi
Measured: Baseline (week 0) to post-training (week 13)
Depressive and anxiety symptoms
The validated version of the HADS for the Brazilian population is used to assess depressive and anxious symptoms (Botega et al., 1995). It is an instrument composed of 14 items, seven of which form the anxiety subscale and the other seven the depression subscale, allowing the assessment of symptoms in the previous week. Each HADS item has four response options ranging from 0 to 3, reaching a maximum of 21 points in each subscale. Participants are instructed to answer the questions based on the last 7 days. Based on the final score of each subscale, participants are categorized as having symptoms of anxiety or depression as "unlikely" (0 to 7 points), "possible" (8 to 11 points), and "probable" (12 to 21 points). Higher scores indicate more severe symptoms and a worse perceived emotional state.
Measured: Baseline (week 0) to post-training (week 13)
Sleep quality
The validated version of the Pittsburgh Sleep Quality Index (PSQI) for the Brazilian population is used to assess subjective sleep quality and related disorders (Bertolazi et al., 2011). The questionnaire consists of 19 items, grouped into seven components: subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disorders, use of sleeping medications, and daytime dysfunction. Each component is scored from 0 (no difficulty) to 3 (severe difficulty), and the sum of the scores results in an overall score ranging from 0 to 21; scores greater than 5 indicate poor sleep quality.
Measured: Baseline (week 0) to post-training (week 13)
Self-reported quality of life
Quality of life is assessed using the WHOQOL-BREF questionnaire, developed by the World Health Organization and previously validated in the Brazilian population (Fleck et al., 2000). The WHOQOL-BREF comprises 26 items divided into four domains: physical, psychological, social relationships, and environment. This instrument is self-administered, with a 5-point Likert scale, and produces standardized scores ranging from 0 to 100, with higher values indicating better perceived quality of life.
Measured: Baseline (week 0) to post-training (week 13)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted5 Sep 2025
- Study start5 Sep 2025 (estimated)
- Primary completionAug 2027 (estimated)
- Study completionAug 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (14)Papers the sponsor has linked to this study.
- Other trials for AgingStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- This trial is a randomized clinical trial employing a 1:1:1 allocation ratio. It was designed as a superiority trial with three parallel groups and blinded to outcome assessors and data analysis.
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 98 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Federal University of Pelotas
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Cristine Lima Alberton, Federal University of Pelotas
- Investigators
- Cristine L Alberton, PhD, Principal investigator, Federal University of Pelotas
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07156708
- Sponsor's protocol ID
- 90526525.0.0000.5313
- Acronym
- WaterCog
- Status last verified
- Sep 2025
- First submitted
- 26 Aug 2025
- Last updated
- 9 Sep 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: Individual participant data can be made available by the Trial Coordinator upon reasonable request.
Publications
Foster C, Florhaug JA, Franklin J, Gottschall L, Hrovatin LA, Parker S, Doleshal P, Dodge C. A new approach to monitoring exercise training. J Strength Cond Res. 2001 Feb;15(1):109-15.
PubMed 11708692Sao-Joao TM, Rodrigues RC, Gallani MC, Miura CT, Domingues Gde B, Godin G. [Cultural adaptation of the Brazilian version of the Godin-Shephard Leisure-Time Physical Activity Questionnaire]. Rev Saude Publica. 2013 Jun;47(3):479-87. doi: 10.1590/s0034-8910.2013047003947. Portuguese.
PubMed 24346560Brucki SM, Nitrini R, Caramelli P, Bertolucci PH, Okamoto IH. [Suggestions for utilization of the mini-mental state examination in Brazil]. Arq Neuropsiquiatr. 2003 Sep;61(3B):777-81. doi: 10.1590/s0004-282x2003000500014. Epub 2003 Oct 28. Portuguese.
PubMed 14595482Fleck MP, Louzada S, Xavier M, Chachamovich E, Vieira G, Santos L, Pinzon V. [Application of the Portuguese version of the abbreviated instrument of quality life WHOQOL-bref]. Rev Saude Publica. 2000 Apr;34(2):178-83. doi: 10.1590/s0034-89102000000200012. Portuguese.
PubMed 10881154Bertolazi AN, Fagondes SC, Hoff LS, Dartora EG, Miozzo IC, de Barba ME, Barreto SS. Validation of the Brazilian Portuguese version of the Pittsburgh Sleep Quality Index. Sleep Med. 2011 Jan;12(1):70-5. doi: 10.1016/j.sleep.2010.04.020. Epub 2010 Dec 9.
PubMed 21145786Botega NJ, Bio MR, Zomignani MA, Garcia C Jr, Pereira WA. [Mood disorders among inpatients in ambulatory and validation of the anxiety and depression scale HAD]. Rev Saude Publica. 1995 Oct;29(5):355-63. doi: 10.1590/s0034-89101995000500004. Portuguese.
PubMed 8731275Heart rate variability. Standards of measurement, physiological interpretation, and clinical use. Task Force of the European Society of Cardiology and the North American Society of Pacing and Electrophysiology. Eur Heart J. 1996 Mar;17(3):354-81. No abstract available.
PubMed 8737210STROOP, J. R. Studies of interference in serial verbal reactions. Journal of Experimental Psychology, v. 18, n. 6, p. 643-662, 1935.
de Paula JJ, Costa DS, Miranda DM, Romano-Silva MA. Brazilian version of the Cognitive Failures Questionnaire (CFQ): cross-cultural adaptation and evidence of validity and reliability. Braz J Psychiatry. 2018 Jul-Sep;40(3):312-315. doi: 10.1590/1516-4446-2017-2227. Epub 2017 Dec 11.
PubMed 29236920Carvalho GA, Caramelli P. Normative data for middle-aged Brazilians in Verbal Fluency (animals and FAS), Trail Making Test (TMT) and Clock Drawing Test (CDT). Dement Neuropsychol. 2020 Jan-Mar;14(1):14-23. doi: 10.1590/1980-57642020dn14-010003.
PubMed 32206193Ross TP, Calhoun E, Cox T, Wenner C, Kono W, Pleasant M. The reliability and validity of qualitative scores for the Controlled Oral Word Association Test. Arch Clin Neuropsychol. 2007 May;22(4):475-88. doi: 10.1016/j.acn.2007.01.026. Epub 2007 Feb 20.
PubMed 17317094Schroeder RW, Twumasi-Ankrah P, Baade LE, Marshall PS. Reliable Digit Span: a systematic review and cross-validation study. Assessment. 2012 Mar;19(1):21-30. doi: 10.1177/1073191111428764. Epub 2011 Dec 6.
PubMed 22156721Alberton CL, Nunes GN, Rau DGDS, Bergamin M, Cavalli AS, Pinto SS. Vertical Ground Reaction Force During a Water-Based Exercise Performed by Elderly Women: Equipment Use Effects. Res Q Exerc Sport. 2019 Dec;90(4):479-486. doi: 10.1080/02701367.2019.1620910. Epub 2019 Jun 11.
PubMed 31184984Alberton CL, Gomes MB, Ferreira HS, de Oliveira FB, Ogonowska-Slodownik A, Gueita-Rodriguez J, Reichert T, Junkes-Cunha M, Pinheiro VHG, Andrade LS. Aquatic exercises combined with cognitive tasks for older women (WaterCog Study): protocol for a randomized clinical trial. BMC Geriatr. 2026 Mar 7;26(1):528. doi: 10.1186/s12877-026-07084-8.
PubMed 41794695
Study at a glance
From the registry record, last updated by the sponsor on 9 Sep 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effects of Aquatic Aerobic Exercises Combined With Cognitive Tasks on Cognitive Function and Other Health-related Outcomes in Older Adults
- ClinicalTrials.gov ID
- NCT07156708
- Acronym / sponsor ID
- WaterCog / 90526525.0.0000.5313
- Conditions
- Aging
- Keywords
- Physical exercise, Physical activity, Dual-task training, Water-based exercise, Cognitive function, Physical fitness, Mental health, Sleep quality
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 98 participants (estimated)
- Lead sponsor
- Federal University of PelotasUniversity, hospital or other
- Study start
- 5 Sep 2025 (estimated)
- Primary completion
- Aug 2027 (estimated)
- Study completion
- Aug 2027 (estimated)
- First posted
- 5 Sep 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 3
- Model description
- This trial is a randomized clinical trial employing a 1:1:1 allocation ratio. It was designed as a superiority trial with three parallel groups and blinded to outcome assessors and data analysis.
| Arm | Type | Receives |
|---|---|---|
| Aquatic aerobic exercise program combined with cognitive tasks | Experimental | Other: Aquatic aerobic exercise program, Other: Cognitive tasks |
| Conventional aquatic aerobic exercise program | Experimental | Other: Aquatic aerobic exercise program |
| Control group | No intervention | – |
Who may qualify
- Ages
- 60 to 75 years
- Sex
- Female only
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (2 listed)
- 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).
Key exclusion criteria (4 listed)
- 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.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Aquatic aerobic exercise programThe aquatic exercise sessions include the following exercises: butt kick, frontal kick, cross-country skiing, and stationary running. These exercises are commonly used in water aerobics classes and provide controlled osteoarticular impact, being safe for older women (Alberton et al., 2019). Training intensity is prescribed using Borg's 6-20 rating of perceived exertion (RPE) scale. The adopted strategy is based on interval training, which alternates between high-intensity effort and low-intensity active recovery phases. Each block consists of 4 minutes of effort (RPE 13 - 15), with one minute for each exercise (butt kick, frontal kick, cross-country skiing, and stationary running) followed by 1 minute of active recovery (RPE 11), performed with stationary running. To facilitate monitoring, an RPE scale (measuring 0.90 × 1.20 m) is fixed to the outside of the pool, in front of the participants. | Other | Aquatic aerobic exercise program combined with cognitive tasks, Conventional aquatic aerobic exercise program |
| Cognitive tasksThis group performs the same aerobic training protocol used by the conventional aquatic program group. Additionally, cognitive tasks are performed during the active recovery phases. Cognitive training encompasses different domains of cognition in all sessions, including semantic fluency, processing speed, cognitive flexibility, inhibitory control, memory, attention, and reasoning. The exercises vary in each class, with progression in complexity in each mesocycle. | Other | Aquatic aerobic exercise program combined with cognitive tasks |
Primary outcome
Objective cognitive function - Digit Span Test
Time frame: Baseline (week 0), post-intervention (week 13), and 12-week follow-up (week 25)
The Digit Span Test is used to assess working memory and attention span (Schroeder et al., 2012). The Digit Span Test requires participants to verbally recall a sequence of numbers dictated by the examiner. The test begins with three numbers ranging from 0 to 9, read at 1-second intervals, which participants must remember in the correct order. The sequence increases by one digit if pronounced correctly. If participants fail to recall the correct sequence twice in a row, the test ends. The number of digits correctly recalled is recorded as the test result, with a higher score indicating better performance.
Objective cognitive function - Controlled Oral Word Association Test
Time frame: Baseline (week 0), post-intervention (week 13), and 12-week follow-up (week 25)
The Controlled Oral Word Association Test (COWAT) is used to assess verbal fluency, working memory, and inhibitory control (Ross et al., 2007). In this test, participants must say as many words as possible that start with the letters "F," "A," and "S" within 1 minute for each letter. Proper names, repeated words, and variations in gender, number, and conjugation are not considered. A higher number of words in each test indicates better verbal fluency.
14 secondary outcomes
Objective cognitive function - Trail Making Test (TMT)
Time frame: Baseline (week 0), post-intervention (week 13), and 12-week follow-up (week 25)
Self-perception of cognitive function
Time frame: Baseline (week 0), post-intervention (week 13), and 12-week follow-up (week 25)
Aerobic fitness
Time frame: Baseline (week 0) to post-training (week 13)
Lower limb strength
Time frame: Baseline (week 0) to post-training (week 13)
Upper limb strength
Time frame: Baseline (week 0) to post-training (week 13)
Lower limb flexibility
Time frame: Baseline (week 0) to post-training (week 13)
Agility and dynamic balance
Time frame: Baseline (week 0) to post-training (week 13)
Dual-task performance
Time frame: Baseline (week 0) to post-training (week 13)
Blood pressure
Time frame: Baseline (week 0) to post-training (week 13)
Blood pressure reactivity
Time frame: Baseline (week 0) to post-training (week 13)
Heart rate variability
Time frame: Baseline (week 0) to post-training (week 13)
Depressive and anxiety symptoms
Time frame: Baseline (week 0) to post-training (week 13)
Sleep quality
Time frame: Baseline (week 0) to post-training (week 13)
Self-reported quality of life
Time frame: Baseline (week 0) to post-training (week 13)
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 9 Sep 2025.
- Background: PubMed 11708692Foster C, Florhaug JA, Franklin J, Gottschall L, Hrovatin LA, Parker S, Doleshal P, Dodge C. A new approach to monitoring exercise training. J Strength Cond Res. 2001 Feb;15(1):109-15.
- Background: PubMed 24346560Sao-Joao TM, Rodrigues RC, Gallani MC, Miura CT, Domingues Gde B, Godin G. [Cultural adaptation of the Brazilian version of the Godin-Shephard Leisure-Time Physical Activity Questionnaire]. Rev Saude Publica. 2013 Jun;47(3):479-87. doi: 10.1590/s0034-8910.2013047003947. Portuguese.
- Background: PubMed 14595482Brucki SM, Nitrini R, Caramelli P, Bertolucci PH, Okamoto IH. [Suggestions for utilization of the mini-mental state examination in Brazil]. Arq Neuropsiquiatr. 2003 Sep;61(3B):777-81. doi: 10.1590/s0004-282x2003000500014. Epub 2003 Oct 28. Portuguese.
- Background: PubMed 10881154Fleck MP, Louzada S, Xavier M, Chachamovich E, Vieira G, Santos L, Pinzon V. [Application of the Portuguese version of the abbreviated instrument of quality life WHOQOL-bref]. Rev Saude Publica. 2000 Apr;34(2):178-83. doi: 10.1590/s0034-89102000000200012. Portuguese.
- Background: PubMed 21145786Bertolazi AN, Fagondes SC, Hoff LS, Dartora EG, Miozzo IC, de Barba ME, Barreto SS. Validation of the Brazilian Portuguese version of the Pittsburgh Sleep Quality Index. Sleep Med. 2011 Jan;12(1):70-5. doi: 10.1016/j.sleep.2010.04.020. Epub 2010 Dec 9.
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- Individual participant dataSharing planned: Yes. Individual participant data can be made available by the Trial Coordinator upon reasonable request.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Cristine L Alberton, PhD principal investigator
Federal University of Pelotas
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Aquatic aerobic exercise program and Cognitive tasks in people with Aging, run by Federal University of Pelotas at 1 site in Brazil.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 9 Sep 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Brazil. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Mariana B Gomes (5553999815166, marianaaaborba@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Objective cognitive function - Digit Span Test (time frame: Baseline (week 0), post-intervention (week 13), and 12-week follow-up (week 25)). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT07156708, which also lists 14 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Sep 2025.