Water Based Burpee Exercises on Functional Capacity in Poste-menopausal Women After Thyroidectomy

November 15, 2025 updated by: Mohamed Saied Zidan, Al-Zaytoonah University of Jordan

Skeletal muscle mass plays an important role with both metabolism and functional capacity. It is well established that the aging process leads to a significant decline in both muscle mass and strength which is associated with frailty , an increased risk of falls and decreased physical fitness and function In this context, high-load resistance training has been shown to reduce the risk of falls and increase strength and functional capacity in middle-aged and/or elderly individuals.

Aquatic exercise is one method that has previously been shown to improve muscle strength, balance, and coordination in those of advancing age Although the evidence supports the effectiveness of both water-based burpee exercise in middle-aged and elderly individuals, has, to our knowledge, never been investigated. Thus, the objective of this study was to assess the long-term effect of water-based burpee exercises

Study Overview

Study Type

Interventional

Enrollment (Estimated)

40

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Adults aged 54 ± 4 years .

    • Post-menopausal women after tyhroidectomy
    • Body mass index (BMI) ≥ 30 kg/m².
    • Absence of osteoarticular dysfunctions in the lower limbs.
    • No personal history of cardiovascular disease
    • No water trauma
    • Non-smokers

Exclusion Criteria:

  • History of Cardiovascular disorders.

    • Severe osteoarticular dysfunctions.
    • Presence of Water panic.
    • Participation in another clinical trial within the last 30 days.
    • Neurologic and psychiatric disorders (spina bifida, cerebral palsy, anorexia nervosa, known autism spectrum disorders).

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Sham Comparator: Control group
Control group will perform traditional aerobic exercises
Traditional aerobic exercises for post-menopause include activities like brisk walking, jogging and cycling. These exercises help improve cardiovascular health, boost metabolism, and enhance mood. They can also be beneficial for maintaining bone density, especially weight-bearing exercises like walking and jogging.
Experimental: Experimental group
Experimental group will perform water based burpee exercises
water based burpee exercises ( Aquatic exercise ) is one method that has previously been shown to improve muscle strength, balance, and coordination in those of advancing age Although the evidence supports the effectiveness of both water-based burpee exercise in middle-aged and elderly individuals, has, to our knowledge, never been investigated. Thus, the objective of this study was to assess the long-term effect of water-based burpee exercises

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
FVC ( liters )
Time Frame: Pre and post 8 weeks
Forced vital capacity (FVC) is the total amount of air exhaled during the FEV test. Forced expiratory volume and forced vital capacity are lung function tests , using portable spirometer ( SP 80B , China )
Pre and post 8 weeks
PEF ( liters / minute )
Time Frame: pre and post 8 weeks
Peak expiratory flow (PEF), a key indicator of lung function,using portable spirometer ( SP 80B,China)
pre and post 8 weeks
FEV1/FVC ( % )
Time Frame: pre and post 8 weeks
Description: The ratio of the forced expiratory volume in the first one second to the forced vital capacity of the lungs. That can reflect pulmonary function , using portable spirometer ( SP 80B,China)
pre and post 8 weeks
FEV1 ( liters )
Time Frame: pre and post 8 weeks
Forced expiratory volume in 1 second that can reflect pulmonary function , using portable spirometer ( SP 80B,China)
pre and post 8 weeks
Chest expansion ( centimeter )
Time Frame: Pre and post 8 weeks
A simple, noninvasive pulmonary function test used to assess chest wall mobility and, to a lesser extent, lung function , using tape measurement.
Pre and post 8 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Timed up and go test ( seconds )
Time Frame: Pre and post 8 weeks
A simple, quick, and widely used clinical performance-based measure of functional mobility and fall risk. It assesses how long it takes for a person to rise from a chair, walk three meters, turn, walk back, and sit down again.
Pre and post 8 weeks
Berg Balance Scale (BBS) to test dynamic balance
Time Frame: Pre and post 8 weeks
A widely used assessment tool in physical therapy to evaluate a patient's functional balance and fall risk. It consists of 14 tasks, scored on a 5-point scale from 0 to 4, with a total possible score of 56. A lower score indicates a higher risk of falling.
Pre and post 8 weeks
Gait Speed ( meters per second ) ( 4 Metre Walk Test )
Time Frame: Pre and post 8 weeks
Is the rate at which a person walks, is typically measured in meters per second (m/s). This is determined by dividing the distance walked by the time it takes to walk that distance. such as ( 4 Metre Walk Test )
Pre and post 8 weeks
30-Second Chair Test ( number of times the patient comes to a full standing position in 30 seconds ).
Time Frame: Pre and post 8 weeks
Designed for testing leg strength and endurance in older adults.
Pre and post 8 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 1, 2025

Primary Completion (Estimated)

November 20, 2025

Study Completion (Estimated)

November 30, 2025

Study Registration Dates

First Submitted

June 26, 2025

First Submitted That Met QC Criteria

June 26, 2025

First Posted (Actual)

July 4, 2025

Study Record Updates

Last Update Posted (Actual)

November 19, 2025

Last Update Submitted That Met QC Criteria

November 15, 2025

Last Verified

November 1, 2025

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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