ClinicalTrials.gg
RecruitingNCT07052279Updated Nov 19, 2025

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

An interventional study of water based burpee exercises and aerobic exercises in Burpee Exercise, Water Exercises and Functional Capacity, sponsored by Al-Zaytoonah University of Jordan. Recruiting at 1 site in Egypt. Open to female participants aged 50 Years to 54 Years. Per ClinicalTrials.gov, last updated 2025-11-19.

Sponsored by Al-Zaytoonah University of Jordan · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Nov 2025, 11 months ago, but the record still lists the study as recruiting.
  • Started Sep 2025; still recruiting 1 year 2 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
50 Years to 54 Years
Sex
Female
01

Study summary

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

02

Conditions studied

  • Burpee Exercise
  • Water Exercises
  • Functional Capacity
  • Postmenopausal
  • Thyroidectomy

Keywords

  • burpee exercises
  • postmenopausal
  • thyroidectomy
03

In context

Lead sponsor

Al-Zaytoonah University of Jordan is the lead sponsor of 31 studies on the registry; 6 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
50 Years to 54 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Adults aged 54 ± 4 years .

    • women after tyhroidectomy
    • (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

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).
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Postmenopausal

Periods have stopped for good: usually no period for 12 months in a row without another medical reason, sometimes confirmed by a blood test (FSH).

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Care provider)
Enrollment
40 participants (estimated)

Study arms

  • Sham comparator
    Control group

    Control group will perform traditional aerobic exercises

    Other: aerobic exercises

  • Experimental
    Experimental group

    Experimental group will perform water based burpee exercises

    Other: water based burpee exercises

Interventions

  • Otherwater 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

  • Otheraerobic 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.

06

What researchers measure

Primary outcomes

  1. FEV1/FVC ( % )

    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)

    Time frame: pre and post 8 weeks

  2. FEV1 ( liters )

    Forced expiratory volume in 1 second that can reflect pulmonary function , using portable spirometer ( SP 80B,China)

    Time frame: pre and post 8 weeks

  3. PEF ( liters / minute )

    Peak expiratory flow (PEF), a key indicator of lung function,using portable spirometer ( SP 80B,China)

    Time frame: pre and post 8 weeks

  4. FVC ( liters )

    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 )

    Time frame: Pre and post 8 weeks

  5. Chest expansion ( centimeter )

    A simple, noninvasive pulmonary function test used to assess chest wall mobility and, to a lesser extent, lung function , using tape measurement.

    Time frame: Pre and post 8 weeks

Secondary outcomes

  1. Timed up and go test ( seconds )

    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.

    Time frame: Pre and post 8 weeks

  2. Gait Speed ( meters per second ) ( 4 Metre Walk Test )

    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 )

    Time frame: Pre and post 8 weeks

  3. 30-Second Chair Test ( number of times the patient comes to a full standing position in 30 seconds ).

    Designed for testing leg strength and endurance in older adults.

    Time frame: Pre and post 8 weeks

  4. Berg Balance Scale (BBS) to test dynamic balance

    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.

    Time frame: Pre and post 8 weeks

07

Study locations

1 of 1 sites recruiting
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Sep 2025 (actual). Primary completion is estimated for Nov 2025, 2 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Jun 26, 2025
First posted
Jul 4, 2025
StartActual
Sep 1, 2025
Primary completionEst.
Nov 20, 2025
CompletionEst.
Nov 30, 2025
Last update
Nov 19, 2025
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Nov 19, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07052279
Lead sponsor
Al-Zaytoonah University of Jordan
Responsible party
Mohamed Saied Zidan (Assistant professor doctor, Al-Zaytoonah University of Jordan) — Principal investigator
First posted
Jul 4, 2025
Start date
Sep 1, 2025
Primary completion
Nov 20, 2025 (estimated)
Completion
Nov 30, 2025 (estimated)
Last update
Nov 19, 2025

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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No contact was published for this record. The registry link below has the sponsor’s details.

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