- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05219227
Effect of Laser Acupuncture Augmented by Abdominal Exercises on Abdominal Fat
Effect of 12 Session of Laser Acupuncture Augmented by Abdominal Exercises on Abdominal Fat in Obese Breast-feeding Women
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Forty breast feeding women aged between 20 and 35 years will recruited to the study in the women health department faculty of physical therapy clinic, kafr el sheikh university , Egypt. The evaluation procedures will explained to each participant. participants will be divided into two groups Group A : received laser acupuncture, diet modification and abdominal exercises Group B: received diet modification and abdominal exercises only
Out come measurement BW, BMI, body fat mass (BFM), body fat percent, waist girth, hip girth, and waist-to-hip ratio (WHR) were measured at baseline and the end of treatment. BW, BMI, BFM, and body fat percent were measured using the body composition analyzer (Model Inbody 3.0, Republic of Korea).
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
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Kafr Ash Shaykh, Egypt, 12511
- Kafar Elsheikh Hospital
-
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- All participants are free from any medical problems such as diabetes mellitus, hypertension and thyroid dysfunction.
All participants do not use any hormonal contraceptive method.
Exclusion Criteria:
- Participants will be excluded if they had diabetes, hypertension, cardiac diseases, patients who had endocrine disease or digestive tract disease and patients with neurological or musculoskeletal disorder.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: body fat mass (BFM)
body fat mass will be measured before and after interventions
|
laser acupuncture on certain point on the abdomen The following abdominal acupuncture points were irradiated: Cv 8 (Shenque), St 25 (Tianshu, bilateral), and Sp 15 (Daheng , bilateral). The laser irradiations were applied directly to the skin of the points with a perpendicular beam. 478 J/cm2 Abdominal exercises: Types of abdominal exercises:
|
|
Experimental: Body mass index (BMI)
BMI will be calculated before and after interventions
|
laser acupuncture on certain point on the abdomen The following abdominal acupuncture points were irradiated: Cv 8 (Shenque), St 25 (Tianshu, bilateral), and Sp 15 (Daheng , bilateral). The laser irradiations were applied directly to the skin of the points with a perpendicular beam. 478 J/cm2 Abdominal exercises: Types of abdominal exercises:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Effect of laser acupuncture and abdominal exercises on Body fat mass
Time Frame: 1 cycle (42 days)
|
Outcome measurement
|
1 cycle (42 days)
|
|
Effect of laser acupuncture and abdominal exercises on Body mass index
Time Frame: 1 cycle (42 days)
|
Outcome measurement
|
1 cycle (42 days)
|
|
Effect of laser acupuncture and abdominal exercises on waist girth, hip girth
Time Frame: 1 cycle (42 days)
|
Outcome measurement
|
1 cycle (42 days)
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- P.T.REC
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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