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Effectiveness of Aquatic Exercises for Improving Mental and Physical Health in Adults.

Effectiveness of Aquatic Exercises for Improving Mental and Physical Health in Adults: Randomized Clinical Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04100850
Acronym
AEforMH
Enrollment
78
Registered
2019-09-24
Start date
2019-08-01
Completion date
2023-12-31
Last updated
2023-05-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety, Depression, Depressive Symptoms

Keywords

hydrotherapy, depression, anxiety

Brief summary

Objective: To compare the effectiveness between aquatic exercises (water aerobics versus Watsu) versus control groups, for improving the outcomes of depression, anxiety, stress, sleep quality, functionality, cognition and quality of life in patients with depression.

Detailed description

Introduction: Considered as the 21st century disease, depression is a silent disease that stands out for its high prevalence and high morbidity, leading to serious consequences. With treatments made in aquatic environment, among them the Water aerobics and Watsu. Objective: To compare the effectiveness between aquatic exercises versus Watsu and versus control group, for improving the outcomes of depression, anxiety, stress, sleep quality, functionality, cognition and quality of life in patients with depression. Methods: This study will be a randomized clinical trial, which will last for two months with a follow-up of one month. All participants will be assessed using specific questionnaires for each outcome and an Improvement Perception Scale (MS). Seventy eight (78) patients with a medical diagnosis of depression, aged 18 to 60 years, who will be allocated to three groups (26 patients for each group) will be treated. GROUP 1: Aquatic exercises (aerobic and resistance), collective session, twice a week lasting 50 min; GROUP 2: Watsu (water shiatsu), individual session, twice a week lasting 50 min; Group 3: control, people with depression. Statistical analysis: Normality distribution will be by Shapiro-Wilk test. For comparisons of the means between and within the outcome groups will be used through Generalized Estimation Equations, with its own syntax, linear distribution and, when necessary, multiple comparisons will be performed using the Bonferroni test to identify differences. Will be calculated for comparisons between the final and initial moments and initial follow-up in each group, statistics such as: mean difference (95% CI), standard deviation of the difference, effect size (Cohen's d). The statistical significance adopted was 5% and the analyzes were performed using the statistical programs SPSS 22.0 and R 3.2.4. The intention-to-treat analysis will be performed.

Interventions

twice a week, lasting 50 minutes, for two months.

OTHERWatsu

twice a week, lasting 50 minutes, for two months.

Sponsors

Universidade Federal do vale do São Francisco
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Intervention model description

Watsu, Aquatic Exercises, Control

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Age between 18 and 60 years old; * Sedentary and who have not had physical therapy and physical activity in the last three months; * Clinical and cognitive conditions for performing pool activities and moderate aerobic exercise; * Who have not undergone high complexity surgical procedures in the last six months; no neuro-musculosqueletal diseases; * No contraindications to exercise; such as: urinary and / or fecal incontinence and dermatological diseases; * Individuals with a medical diagnosis of depression.

Exclusion criteria

* If they have up to three absences during the intervention period; * If they have any adverse effects, such as: allergy or dermatitis; * Unable to continue study due to change of address or hospitalization.

Design outcomes

Primary

MeasureTime frameDescription
Anxietychange anxiety at 8 weeks and follow-up at 12 weeksBeck Anxiety Inventory (better 0-63 worse points)
Depressionchange depression at 8 weeks and follow-up at 12 weeksBeck Depression Inventory (better 0-63 worse points)

Secondary

MeasureTime frameDescription
Quality of Life Questionnairechange quality of live at 8 weeks and follow-up at 12 weeks12-Item Short-Form Health Survey (SF-12) (worse 0 - better 100)
Sleep Qualitychange sleep quality at 8 weeks and follow-up at 12 weeksPittsburgh Sleep Quality Index (PSQI) (better 0 - worse 21)
Cognitivechange cognitive at 8 weeks and follow-up at 12 weeksMontreal Cognitive Assessment (MOCA) (worse 0 - better 30)
Functionallychange functionally at 8 weeks and follow-up at 12 weeksSix-minute Walk Test (6m-WT)
Life Style Scalechange life style at 8 weeks and follow-up at 12 weeksFantastic Life Style Scale (worse 0 - better 100)
Stresschange stress at 8 weeks and follow-up at 12 weeksDepression, Anxiety and Stress Scale (DASS-21) (better 0 - worse \>34)

Other

MeasureTime frameDescription
Improvement Perceptionpos (8 week)Improvement Perception Scale (0-7)

Countries

Brazil

Contacts

Primary ContactRodrigo GS Carvalho, PhD
rodrigocarvalhofisio@gmail.com+5587999832015
Backup ContactRodrigo GS Carvalho, Phd
rodrigo.carvalho@univasf.edu.br+558721016856

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026