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Effects of Aquatic Physical Training Program on Cardiorespiratory Variables in Patients With COPD

Effects of Aquatic Physical Training Program on Cardiorespiratory Variables in Patients With COPD

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02116114
Enrollment
24
Registered
2014-04-16
Start date
2014-05-31
Completion date
2014-12-31
Last updated
2014-04-16

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

Conditions

Adverse Effects in the Aquatic Exercises

Keywords

Pulmonary Disease, Chronic Obstructive

Brief summary

We have as hypothesis that the aquatic aerobic physical training program can help promote beneficial adaptations on the cardiovascular, respiratory and systemic inflammation variables, functional capacity and quality of life in patients with chronic obstructive pulmonary disease (pulmonary emphysema).

Detailed description

First paragraph * aquatic aerobic physical training program * beneficial adaptations Next paragraph * cardiovascular * respiratory * systemic inflammation * functional capacity * quality of life

Interventions

OTHERAerobic training

The program of aquatic exercise training was developed involving the following steps : heating : dynamic stretching exercises aerobic exercises , lasting 10 minutes was performed, aquatic fitness : aerobic training and slowdown. The intensity was prescribed based on the Borg scale score 4-6. Aerobic training was performed at intervals. The duration of aerobic fitness was started with eight 20-minute sessions , progressing to eight sessions of 30 minutes and finished with eight 40-minute sessions. Downturn : global stretching exercises , lasting 10 minutes were performed. During all sessions , the patients were instructed to breath with pursed - lip .

Sponsors

Universidade Metodista de Piracicaba
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
MALE
Age
50 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosis of COPD ( GOLD I / II / III / IV rating ) * Clinically stable * Low level of physical activity , according to the IPAQ ( International Physical Activity Questionnaire ) * Absence of exacerbation in the last three months * Do not participate in a regular exercise program in the past six months

Exclusion criteria

* Diabetes Mellitus * Endocrine Disorders * Chronic renal failure * Liver Diseases * Other lung diseases or inflammatory diseases associated * Cardiac * Use of drugs that prevented physical performance * Musculoskeletal and neuromuscular changes that make it impossible to run experimental protocols * Dermatological disorders ( cutaneous fistulas , infected wounds , ringworm skin , varicose ulcers ) * Hypersensitivity to the product used for the treatment of pool water * Rabies

Design outcomes

Primary

MeasureTime frame
Change from baseline in cardiac autonomic modulation by heart rate variability at week 8Baseline, Week 8

Secondary

MeasureTime frame
Change from baseline in quality of life by the Saint George Respiratory Questionnaire at week 8Baseline, Week 8

Other

MeasureTime frame
Change from baseline in systemic inflammation by C-reactive protein at week 8Baseline, Week 8

Contacts

Primary ContactMarlene A Moreno, PHD
ma.moreno@terra.com.br+55 (19) 31241515

Outcome results

None listed

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