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Combined Effects of Visceral Manipulation and Noble Technique on Post-partum Females With Diastasis Recti

R

Riphah International University

Status

Not yet enrolling

Conditions

Diastasis Recti

Treatments

Other: noble technique
Other: visceral manipulation and noble technique

Study type

Interventional

Funder types

Other

Identifiers

NCT06459752
REC/RCR & AHS/23/0564

Details and patient eligibility

About

Diastasis recti is characterized by an abnormal expansion of the gap between the medial sides of the rectus abdominis muscle and a lengthening of the linea alba (increased inter-recti distance). It is mainly caused by excessive intra-abdominal pressure. The abdominal muscles and connective structures expand from the growing uterus during pregnancy. Low back pain is a prevalent complaint that can result from various factors, including weakened core muscles and functional disability. The aim of the study would assess of combined effect of visceral manipulation and noble technique on Inter-rectal distance, low back pain and functional disability in post-partum females with diastasis recti.

Full description

A randomized controlled trial will be conducted in DHQ Hospital Toba Tek Singh. A nonprobability convenience sampling technique will be used. There will be 34 participants. Participants will meet with inclusion criteria and be divided into two groups A and B. In Group A 17 participants will receive visceral manipulation technique with noble technique for 30 minutes per session, three sessions per week for 6 weeks. While in Group B 17 participants will just receive noble technique exercises for 15 min per session, three sessions per week for 6 weeks. Participants will be assessed before and after treatment through; Digital nylon calipers for diastasis recti, NPRS for pain, and Quebec Back Pain Disability Scale (QBPDS) to assess LBP-related functional. Data will be analyzed during SPSS software version 21

Enrollment

30 estimated patients

Sex

Female

Ages

22 to 35 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age between 22 to 35.
  • Primiparous women with vaginal delivery and an IRD of >2 cm.
  • Three to six months postpartum with the presence of diastasis rectus abdominis.
  • Patients having moderate low back pain in NPRS.

Exclusion criteria

  • Acute Malignancy
  • Recent Abdominal or Pelvic surgery
  • Having undergone spinal surgery in the previous six months
  • Serious spinal pathology
  • Serious cardiovascular or metabolic disease Pregnancy
  • Herniation pain

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

30 participants in 2 patient groups

Group A
Experimental group
Description:
This group received three sessions a week for six weeks, with 30 minutes per session given to visceral manipulation and noble technique (15 minutes each technique).
Treatment:
Other: visceral manipulation and noble technique
Group B
Active Comparator group
Description:
This group receives three sessions a week for six weeks, with 15 minutes per session in which noble technique is applied.
Treatment:
Other: noble technique

Trial contacts and locations

1

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Central trial contact

: Imran Amjad, PhD; Imran Amjad, PhD

Data sourced from clinicaltrials.gov

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