Clinical trial Recruiting at 1 site Interventional Ages 35 to 45 Women only

Treating Diastasis Recti in Postpartum Women with Different Therapies

Official title: Effects of Visceral Manipulation Combined with Kinesio Taping on Diastasis Recti, Pain Intensity, Stress Incontinence, Pelvic Floor Strength, and Overall Wellness in Postpartum Women

Run by Health and Research-Insights · NCT06723353 · Data updated 2026-11-12

This study is testing different therapies to see which one helps new moms with Diastasis Recti feel better and strengthen their abdominal muscles.

More Diastasis Recti trials

Quick facts

Study typeInterventional
Ages35 Years to 45 Years
SexWomen only
Enrollment72 (estimated)
SponsorHealth and Research-Insights
Academic / other
Locations1 site (Karachi, Sindh)
StatusRecruiting
StartedMay 1, 2024
Main results expectedJanuary 31, 2025
Study endsJanuary 31, 2025
Registry record updatedDecember 9, 2024
Trial IDNCT06723353 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are postpartum women aged 35 to 45 who have experienced DRA after childbirth.

Probably not a fit

Patients with other abdominal surgeries, abdominal hernias, or open abdominal wounds may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial evaluates the effectiveness of various therapies for treating Diastasis Recti Abdominis (DRA) in postpartum women. Participants will be randomly assigned to one of four treatment groups: Visceral Manipulation (VM), Kinesio Taping (KT), a combination of both, or core strengthening exercises. The study aims to determine which treatment or combination of treatments most effectively reduces the gap between abdominal muscles and improves associated symptoms such as pain, pelvic floor strength, and urinary incontinence. The interventions will be administered over a six-week period, with assessments conducted to measure outcomes.

Why it matters

Potential benefit: If successful, this study could provide effective treatment options for postpartum women suffering from DRA, improving their physical health and quality of life.

How similar studies have gone: While there is limited data on the specific combination of therapies being tested, similar approaches have shown promise in treating related conditions.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

Post-partum female will be included on the basis of:

* DRA: Finger width palpation shows \>2.5 cm
* Postpartum females bearing at least 1 child
* Age between 35 to 45 years old
* Post-partum females who had gone through normal vaginal delivery, vacuum delivery, forceps delivery, and lower section caesarian section (at least 1 month after)

Exclusion Criteria:

Postpartum female will be excluded if she has:

* Any other abdominal surgery
* Sensitivity with taping (specific for those will have KT)
* Diagnosed with abdominal hernia
* Open abdominal wound

Where it's running

  • Jinnah Postgraduate Medical Center
    Karachi, Sindh, Pakistan
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.