- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07478965
Effects of Acupuncture Versus Deep Breathing Exercises on Hypertensive Pregnant Women in the Third Trimester
March 18, 2026 updated by: Kerolous Ishak Shehata, October 6 University
Effects of Acupuncture Versus Deep Breathing Exercises on Hypertensive Pregnant Women in the Third Trimester. A Randomized Controlled Trial.
investigate the effect of diaphragmatic deep breathing exercises versus acupuncture hypertensive adults This study is expected to provide significant health benefits for pregnant females in the third trimester suffering from hypertension.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The study contributes to lowering the risk of hypertension complications in the pregnant women in the third trimester through a study investigate the effect of diaphragmatic deep breathing exercises versus acupuncture on prehypertensive or hypertensive adults
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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Cairo, Egypt
- Kerolous ishak shehata kelini
-
-
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:
- pregnant women in the third trimester
- suffering from hypertension
- age ranged between 25-35
Exclusion Criteria:
- Uncontrolled diabetes
- Rhumatoid arthritis
- Any respiratory disease like athma
- osteoporosis
- Any kind of infection
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: Acupuncture Group: 20pregnant women received it.
Study group 1: composed of 20 pregnant women received physical therapy session of acupuncture
|
traditional Chinese medicine practice that involves inserting fine needles into specific points on the body to promote healing and balance.
|
|
Experimental: Deep breathing Group:20pregnant women received it.
Study group 2: composed of 20 pregnant women received physical therapy session received Deep breathing exercise
|
Deep breathing exercises can significantly reduce stress and anxiety, improve focus, and enhance overall well-being.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Blood pressure
Time Frame: 2 weeks
|
A sphygmomanometer is an instrument used to measure blood pressure.
Normally value ranged from 100-140 on systole and 60-90 on diastole An inflatable cuff that wraps around the upper arm.
A measuring unit, which can be a mercury manometer or an aneroid gauge, that records the pressure.
|
2 weeks
|
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)
August 27, 2025
Primary Completion (Actual)
November 11, 2025
Study Completion (Actual)
January 20, 2026
Study Registration Dates
First Submitted
March 13, 2026
First Submitted That Met QC Criteria
March 13, 2026
First Posted (Actual)
March 18, 2026
Study Record Updates
Last Update Posted (Actual)
March 23, 2026
Last Update Submitted That Met QC Criteria
March 18, 2026
Last Verified
March 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- P.T- GYN- 01/2026- 574
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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