CClinicalTrials.gg
Not yet recruitingNCT07253844TrA RA IRD DRAUpdated Nov 28, 2025

Effects of Transverse Abdominis Activation and Rectus Abdominis Strengthening on Inter-rectus Distance and Core Stability

An interventional study of Transverse Abdominis activation exercises and Rectus Abdominis Strengthening exercises in Diastasis Recti Abdominis (DRA), sponsored by Lahore University of Biological and Applied Sciences. Not yet recruiting at 2 sites in Pakistan. Open to female participants aged 20 Years to 40 Years. Per ClinicalTrials.gov, last updated 2025-11-28.

Sponsored by Lahore University of Biological and Applied Sciences · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by May 2026, 4 months ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
33
Allocation
Randomized
Ages
20 Years to 40 Years
Sex
Female
01

Study summary

This randomized controlled trial aims to compare the effects of Transverse Abdominis (TrA) activation, Rectus Abdominis (RA) strengthening, and their combined approach on inter-rectus distance (IRD) and core stability in postpartum women diagnosed with diastasis rectus abdominis (DRA). Thirty-three participants will be randomly allocated into three groups and will complete a six-week exercise program at the Pakistan Society for the Rehabilitation of the Disabled (PSRD) Hospital, Lahore. The study will use real-time ultrasound and pressure biofeedback assessment to evaluate changes in IRD and core stability. It is hypothesized that TrA activation and the combined intervention will produce greater improvements compared to RA strengthening alone.

Read the detailed description

Background and Rationale:

Diastasis Rectus Abdominis (DRA) is a prevalent postpartum musculoskeletal condition characterized by the separation of the rectus abdominis muscles along the linea alba, resulting in impaired trunk stability, abdominal weakness, and postural dysfunction. Despite its high prevalence, DRA remains underdiagnosed and undertreated, particularly in developing countries where structured rehabilitation protocols are lacking. Physiotherapy-based interventions focusing on abdominal muscle retraining and core stability have been shown to improve outcomes; however, the relative effectiveness of Transverse Abdominis (TrA) activation, Rectus Abdominis (RA) strengthening, and their combined approach remains uncertain.

Objectives:

This randomized controlled trial aims to compare the effects of TrA activation, RA strengthening, and their combination on inter-rectus distance (IRD) and core stability among postpartum women with DRA.

Methods:

This three-arm, parallel-group randomized controlled trial will be conducted at the Pakistan Society for the Rehabilitation of the Disabled (PSRD) Hospital, Lahore, Pakistan. A total of 33 postpartum women aged 20-40 years, diagnosed with DRA (6 months to 2 years postpartum), will be recruited using non-probability convenience sampling. Participants will be randomly assigned into three groups (n = 11 per group):

Group A (TAA): Transverse Abdominis Activation exercises

Group B (RAS): Rectus Abdominis Strengthening exercises

Group C (TAA + RAS): Combined TrA activation and RA strengthening protocol

Each participant will undergo a 6-week intervention program, including three supervised sessions per week for 3 weeks, followed by a 3-week home exercise program. Each session will last 30-45 minutes and will be supervised by a licensed physical therapist at PSRD.

Outcome Measures:

Primary Outcome: Change in Inter-Rectus Distance (IRD), measured via real-time ultrasound imaging (7.5 MHz linear probe) at three anatomical sites (4.5 cm above, at, and 4.5 cm below the umbilicus), pre- and post-intervention.

Secondary Outcome: Core stability, assessed using a Pressure Biofeedback Unit (PBU) during the abdominal drawing-in maneuver (ADIM) in crook-lying position. Participants will aim to reduce pressure by 6-10 mmHg from a 40 mmHg baseline and sustain the contraction for 10 seconds; the mean of three trials will be recorded.

Randomization and Blinding:

Participants will be randomized using Randomized Allocation Software (Version 1.0) in a 1:1:1 ratio. Due to the exercise-based nature of the interventions, blinding of participants and therapists is not feasible; however, the outcome assessor will remain blinded to group assignments, ensuring a single-blind design.

Data Analysis:

Statistical analysis will be performed using SPSS version 26. Data will first be tested for normality using the Shapiro-Wilk test. A two-way mixed ANOVA will be applied to assess both within-subject effects (time: pre vs. post) and between-subject effects (group: TAA, RAS, TAA+RAS), as well as the interaction effect (time × group) on IRD and core stability outcomes. Post-hoc pairwise comparisons with Bonferroni correction will identify specific between-group differences. Statistical significance will be set at p \< 0.05 with a 95% confidence interval.

Expected Clinical Significance:

It is hypothesized that TrA activation exercises will lead to a greater reduction in IRD and improvement in core stability compared to RA strengthening alone. The combined exercise group (TAA + RAS) is expected to demonstrate the most comprehensive benefits due to synergistic activation of both deep and superficial abdominal muscles. The study outcomes are anticipated to provide evidence-based guidance for physiotherapists in postpartum rehabilitation, contributing to the development of standardized, non-invasive exercise protocols for DRA management and improved quality of life in postpartum women.

02

Conditions studied

  • Diastasis Recti Abdominis (DRA)

Keywords

  • Diastasis Rectus Abdominus
  • Inter rectus distance
  • Rectus abdominus strenghtheing
03

In context

Lead sponsor

Lahore University of Biological and Applied Sciences is the lead sponsor of 75 studies on the registry; 55 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years to 40 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Inclusion criteria

. Postpartum women diagnosed with DRA

  • Multigravida
  • Delivered a singleton pregnancy via vaginal breech or instrumental delivery

Exclusion criteria

Exclusion Criteria:

. Pregnancy

  • Abdominal and pelvic hernias or severe musculoskeletal conditions
  • Patients with abdominal and pelvic surgery
  • Patients with disc herniation
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
33 participants (estimated)

Study arms

  • Experimental
    Group A (Transverse abdominis activation)

    Other: Transverse Abdominis activation exercises

  • Experimental
    Group B (Rectus abdominis strengthening)

    Other: Rectus Abdominis Strengthening exercises

  • Experimental
    Group C (Transverse abdominis activation +rectus abdominis strengthening)

    Other: combined protocol of both transverse abdominis activation and rectus abdominis strengthening.

Interventions

  • OtherTransverse Abdominis activation exercises

    Group A (TAA) will perform abdominal drawing-in maneuvers (ADIM) in crook lying, side lying, and quadruped positions. They will be instructed to gently draw the belly button inward toward the spine without moving the pelvis or rib cage, emphasizing breathing coordination and pelvic floor co-activation. In the supervised phase, participants will perform 3 sets of 10 repetitions, with each contraction held for 10-20 seconds, and a rest interval of 3 minutes between sets

  • OtherRectus Abdominis Strengthening exercises

    Group B (RAS) will perform exercises in supine lying with knees bent, including partial curl-ups, reverse crunches, pelvic tilts, and leg raises with abdominal bracing. The command will be tighten your abdominals as if bracing for a punch, and lift without straining your neck. Each supervised session will include 3 sets of 10-15 repetitions per exercise, progressing in difficulty using added resistance if tolerated, with a 3-minute rest interval between sets

  • Othercombined protocol of both transverse abdominis activation and rectus abdominis strengthening.

    Group C (TAA+RAS) will perform a hybrid protocol integrating both TrA activation and RA strengthening exercises. Each session will begin with ADIM in crook lying, side lying, and quadruped positions, followed by RA exercises including curl-ups, pelvic tilts, and leg raises. The command will be to activate your deep core with breathing, then strengthen your outer abdominals through controlled movements. Each supervised session will consist of 3 sets of 10 repetitions for TrA exercises (10-20 seconds hold) and 3 sets of 10-15 repetitions for RA exercises, with a rest period of 3 minutes between all sets.

06

What researchers measure

Primary outcomes

  1. Inter-rectus Distance (IRD)

    The Inter-rectus Distance (IRD) is the measurement of the separation between the two rectus abdominis muscles along the linea alba. It is assessed using ultrasound imaging while the participant is in a supine position with knees bent.. A high-frequency (7.5 MHz) linear probe will be placed on the abdomen while the patient lies on their back. Images will be taken at three points above, at, and below the belly button.

    Time frame: Baseline: Before starting the intervention Post-intervention: At the end of 6 weeks of the exercise program

Secondary outcomes

  1. Core stability

    core stability was assessed using the pressure biofeedback unit (PBU), a reliable and non-invasive tool designed to evaluate the activation and control of deep abdominal muscles, particularly TrA. The PBU consists of a pressure cuff connected to an analog pressure gauge and provides visual feedback on pressure changes in response to subtle lumbo pelvic movements (57). For assessment, participants were positioned in a crook lying position, and the cuff was positioned under the lumbar spine (L4-L5 region). The device was inflated to a baseline pressure of 40 mmHg, and participants will be instructed to perform the abdominal drawing-in maneuver, aiming to reduce the pressure by 6-10 mmHg without moving the pelvis or spine. They were asked to maintain this contraction for 10 seconds, and the procedure will be repeated three times, with the average score recorded for analysis.

    Time frame: Baseline (pre-intervention) and 6 weeks (post-intervention)

07

Study locations

2 sites
  • Lahore University of biological and applied sciences
    Lahore, Punjab Province, Pakistan
  • Pakistan Society for Rehabilitation of Differently Abled
    Lahore, Punjab Province, Pakistan
08

References and documents

Publications

  • Benjamin DR, Frawley HC, Shields N, van de Water ATM, Taylor NF. Relationship between diastasis of the rectus abdominis muscle (DRAM) and musculoskeletal dysfunctions, pain and quality of life: a systematic review. Physiotherapy. 2019 Mar;105(1):24-34. doi: 10.1016/j.physio.2018.07.002. Epub 2018 Jul 24. PubMed 30217494 ↗
  • Olsson A, Woxnerud K, Kiwanuka O, Sandblom G, Stackelberg O. The TOR concept (training, operation, and rehabilitation) applied to a cohort of postpartum women with training-resistant symptomatic rectus diastasis: evaluation 1 year after surgery. BJS Open. 2023 Jan 6;7(1):zrac162. doi: 10.1093/bjsopen/zrac162. PubMed 36734959 ↗
  • Gluppe SL, Hilde G, Tennfjord MK, Engh ME, Bo K. Effect of a Postpartum Training Program on the Prevalence of Diastasis Recti Abdominis in Postpartum Primiparous Women: A Randomized Controlled Trial. Phys Ther. 2018 Apr 1;98(4):260-268. doi: 10.1093/ptj/pzy008. PubMed 29351646 ↗
  • Pascoal AG, Dionisio S, Cordeiro F, Mota P. Inter-rectus distance in postpartum women can be reduced by isometric contraction of the abdominal muscles: a preliminary case-control study. Physiotherapy. 2014 Dec;100(4):344-8. doi: 10.1016/j.physio.2013.11.006. Epub 2014 Jan 18. PubMed 24559692 ↗
  • Berg-Poppe P, Hauer M, Jones C, Munger M, Wethor C. Use of exercise in the management of postpartum diastasis recti: a systematic review. The Journal of Women's & Pelvic Health Physical Therapy. 2022;46(1):35-47.

Individual participant data

Plan to share: Yes — De-identified individual participant data (IPD) will be shared, including demographic characteristics (age, parity, BMI), baseline and post-intervention ultrasound measurements of inter-rectus distance (IRD), abdominal muscle strength scores, and functional outcome or patient-reported measures related to abdominal function. Data will also include group allocation (Transverse Abdominis Activation or Rectus Abdominis Strengthening) for analysis comparison. All shared data will be stripped of any personal identifiers to ensure participant confidentiality. The shared dataset will be available in a coded format for secondary analysis and research transparency purposes only.

Supporting information: Study protocol, Sap, Icf, Csr

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 28, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07253844
Lead sponsor
Lahore University of Biological and Applied Sciences
Responsible party
Sponsor
First posted
Nov 28, 2025
Start date
Nov 25, 2025 (estimated)
Primary completion
May 25, 2026 (estimated)
Completion
May 30, 2026 (estimated)
Last update
Nov 28, 2025

Study contacts

Attia Mehboob, Doctor of Physical Therapy
Contact
attiakhan455@gmail.com
+923230016002
Muhammad Tariq Shafi, BSPT, t-DPT
Contact
muhammad.tariq@ubas.edu.pk
+923454190056
Muhammad tariq Shafi, BSPT,tDPT
study chair · Lahore University of Biological and Applied Sciences

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Nov 2025. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion