- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07291440
Impact of Balneotherapy in Ma'n Hot Spring on Quality of Life in Adults With Low Back Pain
December 19, 2025 updated by: Kerolous Ishak Shehata, October 6 University
Impact of Balneotherapy in Ma'n Hot Spring on Quality of Life in Adult With Low Back Pain: Randomized Clinical Trial
Effect of Ma'n hot spring on quality of life in adults with low back pain
Study Overview
Detailed Description
Effect of Ma'n hot spring on quality of life in adults with low back pain
Study Type
Interventional
Enrollment (Actual)
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
-
-
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Amman, Jordan
- Al-Zaytoonah University
-
-
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
- Child
- Adult
Accepts Healthy Volunteers
No
Description
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
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: Factorial Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Aerobic exercise
The study group will perform regular aerobic exercise on mat
|
The core is a box structure made up of the abdominal muscles in the front and the sides, the paraspinal and gluteal muscles at the back, the diaphragm at the roof, and the pelvic floor and the hip girdle muscles as the floor.
|
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Experimental: Ma'n hot spring
The experimental group will perform underwater exercise in Ma'n hot spring
|
The core is a box structure made up of the abdominal muscles in the front and the sides, the paraspinal and gluteal muscles at the back, the diaphragm at the roof, and the pelvic floor and the hip girdle muscles as the floor.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Visual analogue scale
Time Frame: Before starting aerobic exercise and after 6 weeks of performing 12 sessions
|
It is a scale ranged from zero to ten and zero point indicate there is no pain and ten point indicate the worst pain
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Before starting aerobic exercise and after 6 weeks of performing 12 sessions
|
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Biofeedback
Time Frame: Start before starting aerobic exercise and after 6 weeks of performing 12 sessions
|
Biofeedback is a valuable tool for assessing and training muscle power in the lower back region.
It involves using pressure biofeedback units to measure the strength of core muscles such as the transversus abdominis and lumbar multifidi.
Pressure ranged from zero to 100 and zero point means weak muscle and 100 means high power muscle
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Start before starting aerobic exercise and after 6 weeks of performing 12 sessions
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Kerolous IS Kelini, Al-Zaytoonah University
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)
June 1, 2025
Primary Completion (Actual)
October 18, 2025
Study Completion (Actual)
November 20, 2025
Study Registration Dates
First Submitted
December 5, 2025
First Submitted That Met QC Criteria
December 5, 2025
First Posted (Estimated)
December 18, 2025
Study Record Updates
Last Update Posted (Actual)
December 29, 2025
Last Update Submitted That Met QC Criteria
December 19, 2025
Last Verified
December 1, 2025
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- IRB#27\9\2025-2026
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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