- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07719335
Effect of Combined Program of Electro Acupuncture With Exercise on Symphysis Pubis Dysfunction During Pregnancy
July 18, 2026 updated by: Eman Awad, Beni-Suef University
Effect of Combined Program of Electro Acupuncture With Exercise on Symphysis Pubis Dysfunction During Pregnancy: A Randomized Controlled Trial
Study's Objective: this study aimed to discover the effect of combining electroacupuncture with therapeutic exercises on of symphysis pubis dysfunction during pregnancy.A prospective randomized controlled trial that compared 2 groups of participants was executed.
60 primipara and multipara pregnant women at 25-28 weeks' of gestation diagnosed with symphysis pubis dysfunction were involved.
Group A included participants who joined six-week physiotherapy sessions composed of electroacupuncture technique combined with relevant therapeutic exercise, wore a pelvic belt and received pieces of advice.
While, group B involved control participants who followed the routine care and received advice as well as put on the same pelvic belt as group A participants.The intervention was associated with a statistically significant pain reduction and much less progression of inter-pubic gap widening among group A participants.In summary, electroacupuncture should be integrated into a multimodal care plan, combining stabilizing exercises and ergonomic advice, while adhering to the listed safety exclusions to improve quality of life for women suffering from symphysis pubis dysfunction during pregnancy.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
60
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
-
-
-
Banī Suwayf, Egypt
- Beni-Suef 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
- Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- 60 primipara and multipara pregnant women at 25-28 weeks' of gestation diagnosed with symphysis pubis dysfunction were involved. Their ages ranged from 25-40 years and their body mass index (BMI) did not surpass 35 kg/m2.
Exclusion Criteria:
- Exclusion criteria included participants who were diagnosed with placenta previa, unexplained vaginal bleeding, or active preterm labor, as well as patients with a history of recurrent miscarriage, cervical insufficiency, or current multiple gestation.12,13 Additionally, patients with the presence of a cardiac pacemaker, implanted defibrillator, or seizure disorder because of electromagnetic interference and the potential to lower the seizure threshold.14 Cutaneous infection, severe edema, or dermatitis over the intended needling sites were also exclusion criteria, as they increase the likelihood of local complications and systemic spread of infection.15 Coagulopathies, thrombocytopenia, or current anticoagulant therapy represent absolute contraindications for electro acupuncture.16
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: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: No Intervention
Placebo Group routine pelvic belt as well as advice
|
|
|
Experimental: Intervention group
Intervention group participants
|
physiotherapy plan of care in the form of sessions composed of electroacupuncture technique combined with relevant therapeutic exercise, wore a pelvic belt and received pieces of advice.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Symphysis Pubis Width
Time Frame: 4 months
|
It was described by inter-pubic gap space measured in millimetres by means of ultrasonically before and after 6 weeks of intervention procedure.
|
4 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
December 11, 2025
Primary Completion (Actual)
May 12, 2026
Study Completion (Actual)
May 16, 2026
Study Registration Dates
First Submitted
July 18, 2026
First Submitted That Met QC Criteria
July 18, 2026
First Posted (Actual)
July 22, 2026
Study Record Updates
Last Update Posted (Actual)
July 22, 2026
Last Update Submitted That Met QC Criteria
July 18, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- FMBSUREC/02122025A/Awad
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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.
Clinical Trials on Pregnancy Complications
-
University Hospital, MontpellierInstitut National de la Santé Et de la Recherche Médicale, FranceNot yet recruiting
-
Kafrelsheikh UniversityNot yet recruitingEctopic PregnancyEgypt
-
Meir Medical CenterRecruiting
-
Bagcilar Training and Research HospitalRecruitingEctopic PregnancyTurkey (Türkiye)
-
Northwestern UniversityTerminatedPregnancy Related | Labor ComplicationUnited States
-
The George Washington University Biostatistics...Eunice Kennedy Shriver National Institute of Child Health and Human Development...Terminated
-
Oslo University HospitalRecruitingPregnancy Related | Labor Complication | Induced; BirthNorway
-
University of PennsylvaniaRecruitingEarly PregnancyUnited States
-
Beni-Suef UniversityCompletedPregnancy ComplicationsEgypt
-
Medical College of WisconsinBill and Melinda Gates FoundationRecruiting
Clinical Trials on Electroacupuncture Technique and Stabilizing Exercises
-
Riphah International UniversityRecruitingPrimary DysmenorrheaPakistan
-
University of HailTaif UniversityCompletedImpingement Syndrome of AnkleSaudi Arabia
-
Mansoura UniversityCompletedTemporomandibular Joint Disc Displacement | Internal Derangement of the Tempromandibular Joint | Temporomandibular Disorders (TMDs) | Myogenic Temporomandibular Joint DisordersEgypt
-
Norwegian University of Science and TechnologySt. Olavs Hospital; Norwegian Fund for Postgraduate Training in PhysiotherapyCompletedCerebrovascular AccidentNorway
-
Kirsehir Ahi Evran UniversitesiCompletedCarpal Tunnel SyndromeTurkey
-
Riphah International UniversityNot yet recruitingIdiopathic ScoliosisPakistan
-
Riphah International UniversityCompletedDiastasis Rectus AbdominisPakistan
-
Cairo UniversityRecruiting
-
Riphah International UniversityRecruiting
-
Dow University of Health SciencesRecruiting