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Active, not recruitingNCT07929727Updated Nov 10, 2026

Effects of TENS With and Without Core Stabilization Exercises on Low Back Pain, Inter-Recti Distance, and Transversus Abdominis Thickness in Postpartum Women With Diastasis Recti Abdominis

An interventional study of Transcutaneous Electrical Nerve Stimulation (TENS) alone. and TENS combined with Core Stabilization Exercises in Diastasis Recti Abdominis (Postpartum), sponsored by University of Management and Technology Lahore. Active, not recruiting at 1 site in Pakistan. Open to female participants aged 21 Years to 45 Years. Per ClinicalTrials.gov, last updated 2026-11-10.

Sponsored by University of Management and Technology Lahore · Not applicable, Interventional, and Treatment

Updated Nov 10, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
36
Allocation
Randomized
Ages
21 Years to 45 Years
Sex
Female
01

Study summary

Low back pain is a common complaint among postpartum females, often associated with diastasis recti abdominis (DRA), a condition characterized by the separation of the rectus abdominis muscles. This separation can lead to reduced core stability, altered biomechanics, and impaired functional performance. Effective rehabilitation strategies are essential to address pain, restore abdominal muscle integrity, and improve overall function in this population. This study aims to investigate the effects of Transcutaneous Electrical Nerve Stimulation (TENS) with and without core stabilization exercises on low back pain, inter-recti distance (IRD), and transversus abdominis (TrA) thickness in postpartum females with diastasis recti abdominis. A randomized clinical trial will be conducted in which participants will be divided into two groups: one receiving TENS alone and the other receiving TENS combined with core stabilization exercises. Outcome measures will include pain intensity assessed through standardized scales, inter-recti distance measured using musculoskeletal ultrasound, and transversus abdominis thickness evaluated at rest and during contraction. These measures will be recorded before and after the intervention period to determine treatment effectiveness. Group A will receive TENS for pain relief.

Group B will receive TENS combined with core stabilization exercises such as abdominal drawing-in, pelvic tilts, and bridging for 4-6 weeks. Data will be analyzed using SPSS. Paired t-tests will assess within-group changes, and independent t-tests will compare between groups. A p-value ≤ 0.05 will be considered significant. The findings of this study are expected to provide evidence regarding the added benefit of core stabilization exercises when combined with TENS in postpartum rehabilitation.

This may help in developing more effective physiotherapy protocols for managing low back pain and abdominal muscle dysfunction in females with diastasis recti abdominis.

02

Conditions studied

  • Diastasis Recti Abdominis (Postpartum)

Keywords

  • Inter recti distance,
  • Core stabilization exercises,
  • Transcutaneous electrical nerve stimulation,
  • abdominal muscle separation,
  • transversus Abdominus thickness
03

In context

Lead sponsor

University of Management and Technology Lahore is the lead sponsor of 39 studies on the registry; 20 are open to participants now.

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

04

Who can participate

Ages eligible
21 Years to 45 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients diagnosed with Diastasis Recti Abdominis (DRA).

    • Inter-recti distance of ≥2 cm confirmed by clinical examination
    • Pain intensity ≥4 on the Numeric Pain Rating Scale (NPRS).
    • Females aged 21-45 years
    • Postpartum females at least 6 weeks after delivery.
    • Not undergoing any other physiotherapy treatment for DRA

Exclusion criteria

Exclusion Criteria:

    • Previous abdominal surgery within the last 6 months.

      • Presence of abdominal hernia requiring surgical intervention.
      • Pregnancy or high-risk pregnancy.
      • Neurological disorders affecting trunk muscle function.
      • Severe musculoskeletal disorders limiting participation in exercise.
      • Cardiac pacemaker or other implanted electrical devices contraindicating the use of TENS
05

Study design

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

Study arms

  • Experimental
    Transcutaneous Electrical Nerve Stimulation (TENS) alone,

    Continuous mode (burst mode), frequency 80-100 Hz, pulse duration 100-150 μs, intensity adjusted to a comfortable sensory level without muscle contraction, applied for 20 minutes. The intervention will be administered 3 sessions per week for 6 weeks..

    Other: Transcutaneous Electrical Nerve Stimulation (TENS) alone.

  • Active comparator
    TENS combined with Core Stabilization Exercises

    Participants will receive TENS using the same parameters as Group A for 20 minutes. Abdominal drawing-in maneuver: 3 sets × 10 repetitions .Pelvic tilts: 3 sets × 10 repetitions . Heel slides: 3 sets × 10 repetitions Bridging exercises: 3 sets × 10 repetitions. The intervention will be administered 3 sessions per week for 6 weeks.

    Other: TENS combined with Core Stabilization Exercises

Interventions

  • OtherTranscutaneous Electrical Nerve Stimulation (TENS) alone.

    Continuous mode (burst mode), frequency 80-100 Hz, pulse duration 100-150 μs, intensity adjusted to a comfortable sensory level without muscle contraction, applied for 20 minutes. The intervention will be administered 3 sessions per week for 6 weeks..

  • OtherTENS combined with Core Stabilization Exercises

    Participants will receive TENS using the same parameters as Group A for 20 minutes. Abdominal drawing-in maneuver: 3 sets × 10 repetitions .Pelvic tilts: 3 sets × 10 repetitions . Heel slides: 3 sets × 10 repetitions Bridging exercises: 3 sets × 10 repetitions. The intervention will be administered 3 sessions per week for 6 weeks.

06

What researchers measure

Primary outcomes

  1. DIGITAL VERNIER CALIPER

    A Digital Vernier Caliper is a precision measuring instrument used to measure linear distances accurately. In patients with Diastasis Recti Abdominis (DRA), it can be used to assess the Inter-Recti Distance (IRD), which is the separation between the two rectus abdominis muscles. The device provides measurements in millimeters (mm) and offers high accuracy and reliability for clinical assessment.

    Time frame: baseline and after 6 weeks

  2. MSK ULTRASOUND

    Musculoskeletal Ultrasound (MSK-US) is a real-time, non-invasive imaging tool used to measure the thickness and activation of the Transversus Abdominis (TrA), especially in postpartum females with Diastasis Recti.

    Time frame: baseline and after 6 weeks

  3. OSWESTRY DISABILITY INDEX

    The Oswestry Disability Index (also known as the Oswestry Low Back Pain Disability Questionnaire) is an extremely important tool that researchers and disability evaluators use to measure a patient's permanent functional disability. The test is considered the "gold standard" of low back functional outcome tools.

    Time frame: baseline and after 6 weeks

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: Yes — The results data collected , de-identified individual participant data will be shared.

Supporting information: Study protocol, Statistical analysis plan, Informed consent form

Time frame: 6 months after the publication of the manuscript.

Access criteria: The data can be requested from the corresponding author.

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Nov 10, 2026
Show all 1 update
  1. Nov 10, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07929727
Lead sponsor
University of Management and Technology Lahore
Responsible party
Tamknat Ilyas (ASSISTANT PROFESSOR, University of Management and Technology Lahore) — Principal investigator
First posted
Nov 10, 2026
Start date
Nov 5, 2026
Primary completion
Dec 31, 2026 (estimated)
Completion
Dec 31, 2026 (estimated)
Last update
Nov 10, 2026

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 active, not recruiting, as verified in Nov 2026. You cannot join it, but the record below documents what was studied.

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