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Recruiting NCT07132736

Impact of Underwater Exercise Versus Regular Aerobic Exercise on Quality of Life and Power of Muscle

No phase Interventional Muscle Weakness | Patient Quality of Life

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Hubbard tank, Mat on the ground.
Who it may be relevant to
Registry conditions: Muscle Weakness | Patient, Quality of Life. Basic parameters: 18 years — 50 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Jordan
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

To investigate the Impact of underwater exercise versus regular aerobic exercise on quality of life and power of muscle

Detailed description

To ensure statistical power and the reliability of results, the study will involve a sample size of sixty women between 16 and 50 years of age were randomly divided into an experimental and a study group (30 members each).

The experimental group will perform underwater exercise and the study group will perform regular aerobic exercise

Interventions

  • Device Hubbard tank
    women will perform pelvic floor exercise and core stability exercise under water each session will be for 30 min
  • Other Mat on the ground
    women will perform core stability exercise and pelvic floor exercise on the mat for 30 min

Primary outcome measures

  • Visual analogue scale [Time frame: The evaluation took place through study completion on 2 months]
  • Dynamomoter [Time frame: The evaluation took place through study completion on 2 months]
  • Psychological rating scale [Time frame: The evaluation took place through study completion on 2 months]

Eligibility criteria

Inclusion criteria

  • BMI> 25
  • low muscle power
  • low quality of life
  • general fatigue

Exclusion criteria

  • BMI< 25
  • Polycystic ovarian syndrome
  • Chronic pelvic pain
  • Lumbar disc

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Treatment

Study locations

Jordan · 1 center
  • Kerolous ishak shehata kelini — Amman

Identifiers

NCT: NCT07132736 · IRB # 11/6/2024-2025

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗