NCT07572786

Brief Summary

Postpartum constipation is a common condition affecting women after childbirth, leading to discomfort and reduced quality of life. Pharmacological treatments may have side effects and are sometimes avoided during breastfeeding. Electroacupuncture is a safe, non-pharmacological intervention that may improve bowel motility. However, limited evidence exists regarding its effectiveness in postpartum women, necessitating further investigation

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
5mo left

Started May 2026

Shorter than P25 for not_applicable

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 1, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

May 7, 2026

Completed
13 days until next milestone

Study Start

First participant enrolled

May 20, 2026

Expected
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 20, 2026

2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

October 20, 2026

Last Updated

May 7, 2026

Status Verified

May 1, 2026

Enrollment Period

3 months

First QC Date

May 1, 2026

Last Update Submit

May 1, 2026

Conditions

Outcome Measures

Primary Outcomes (2)

  • Bristol Stool Form Scale

    This scale will be used to assess stool consistency, which is classified into seven distinct types ranging from hard lumps to entirely liquid stool. It is considered an important indicator of intestinal transit time. The Bristol Stool Form Scale is widely validated and demonstrates high reliability and reproducibility in clinical and research settings. In this study, it will be used as a primary outcome measure to evaluate changes in bowel habits, either independently or alongside bowel movement frequency.

    6 weeks

  • Patient Assessment of Constipation Quality of Life (PAC-QOL)

    This questionnaire will be used to evaluate the impact of constipation on patients' daily life, including physical discomfort, psychosocial effects, and overall satisfaction. The PAC-QOL has excellent psychometric properties, including strong validity and reliability. In this study, it will be used as a secondary outcome measure to assess improvements in quality of life following the intervention.

    6 weeks

Study Arms (2)

electro acupuncture group

EXPERIMENTAL

Participants in this group will receive electroacupuncture therapy applied to Quchi (LI11) and Shangjuxu (ST37) acupoints plus abdominal exercises Treatment will be administered \[12 sessions per week\] for \[6 weeks\], with each session lasting approximately \[30 minutes\]. The intervention aims to improve bowel function in postpartum constipation.

Other: electroacupunctureOther: abdominal exercises for constipation

control group

ACTIVE COMPARATOR

Participants in this group will perform a structured abdominal exercise program designed to improve bowel motility. Exercises will be conducted \[12 sessions per week\] for \[6 weeks\], with each session lasting approximately \[20 minutes\].

Other: abdominal exercises for constipation

Interventions

This study is expected to contribute significantly to maternal healthcare in Egypt by addressing postpartum constipation, a common yet often neglected condition affecting women after childbirth. Constipation can negatively impact quality of life, causing discomfort, pain, and psychological distress. Electroacupuncture offers a safe, non-pharmacological, and cost-effective treatment alternative. This is particularly important for postpartum women who may avoid medications due to breastfeeding concerns or side effects. The findings of this study may support the integration of electroacupuncture into routine postpartum care in Egypt, especially within physical therapy and rehabilitation programs. It may also help reduce dependence on laxatives and improve patient satisfaction.

electro acupuncture group

Static Abdominal Contractions Lie on your back in "crook lying" (knees bent, feet flat). Gently contract all abdominal muscles (as if bracing for a light punch), hold 5-10 seconds, then release. Repeat. Keep breathing normally. This strengthens the abdominal wall to improve bowel support and tone. Activation and exercise of the transverse abdominis muscle has been noted as important, as it brings together the bellies of the rectus abdominus muscle, improving the integrity of the linea alba and increasing fascial tension. While studied primarily for diastasis recti, these exercises engage the deep core and can support improved abdominal function overall.

control groupelectro acupuncture group

Eligibility Criteria

Age20 Years - 40 Years
Sexfemale(Gender-based eligibility)
Gender Eligibility Detailspostpartum constipated females
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Females aged 20-40 years
  • Within 6 weeks postpartum
  • Diagnosed with constipation
  • Willing to participate

You may not qualify if:

  • History of gastrointestinal disorders
  • Previous colorectal surgery
  • Neurological diseases affecting bowel function
  • Contraindications to acupuncture (tumor, scar or keloids \& spinal instability ).

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Interventions

Electroacupuncture

Intervention Hierarchy (Ancestors)

Combined Modality TherapyTherapeuticsAcupuncture TherapyComplementary TherapiesElectric Stimulation TherapyPhysical Therapy ModalitiesRehabilitationTranscutaneous Electric Nerve StimulationAnalgesiaAnesthesia and AnalgesiaAnesthesia

Central Study Contacts

shaimaa MH elmarakby

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Masking Details
The study is assessor-blinded. The individual responsible for outcome evaluation will not be informed of group allocation. Participants and therapists delivering the interventions will be aware of the assigned treatment due to the practical limitations of the study design.
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Participants will be randomized into two parallel groups: an electroacupuncture group and a control group that will receive abdominal exercises. Both groups will undergo interventions over the same period, and outcomes will be evaluated before and after treatment.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Lecturer

Study Record Dates

First Submitted

May 1, 2026

First Posted

May 7, 2026

Study Start (Estimated)

May 20, 2026

Primary Completion (Estimated)

August 20, 2026

Study Completion (Estimated)

October 20, 2026

Last Updated

May 7, 2026

Record last verified: 2026-05