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Effects of Core Stabilization Exercises and Myofascial Induction Therapy in Postpartum Low-back Pain

Combine Effects of Core Stabilization Exercises and Myofascial Induction Therapy on Lumber Pain, Core Endurance and Quality of Life in Postpartum Low-back Pain

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07576244
Enrollment
40
Registered
2026-05-08
Start date
2025-10-01
Completion date
2026-07-01
Last updated
2026-05-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Low Back Pain

Keywords

Exercises, Low-back pain, Postpartum, Quality of life, Induction therapy

Brief summary

The aim of this study is to determine the combine effects of core stabilization exercises and Myofascial Induction therapy on lumber pain, core endurance and quality of life on postpartum low-back pain.

Detailed description

A randomized controlled trial will be conducted at Bashir Hospital and Fatima Hospital, Sialkot recruiting 40 female patients (aged between 20-45 years) with postpartum low back pain. Participants will be randomly assigned into two groups using a non-probability convenience sampling technique. The Experimental group A will receive myofascial induction therapy along with core stabilization exercises thrice a week for a total of 8 weeks, and the Control group B will receive only core stabilization exercises three times a week for a total of 8 weeks. Both groups will also receive baseline treatment that includes a hot pack and TENS for 15 minutes. Outcome measures include lumbar pain, core endurance and quality of life will be measured by using the Numeric Pain Rating Scale (NPRS), Supine Bridge test and the Short Form health survey (SF-36) and. Data will be analyzed by SPSS version 21. Outcome measures will be assessed pre-test and post-test.

Interventions

OTHERCORE STABILIZATION EXERCISES

Total 5 sets will perform and each set contain 10 repetitions with rest period of 10 sec between each set. Three sessions will be given per week for a total of 8 weeks and each session will be of 30- 45 mins

All of the MIT techniques, will applied to the patients for a total of 40 min in a session, three time per week for eight weeks

Sponsors

Riphah International University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* Will have a NPRS scoring ranging 3-8 * Female with normal vaginal delivery (SVD) * Patients within 6 months of postpartum * BMI \< 30 kg/ m2

Exclusion criteria

* Spinal fracture or deformity * Arthritis * Lumber radiculopathy * Inflammatory condition that cause low back pain * Severe discopathy

Design outcomes

Primary

MeasureTime frameDescription
Numeric Pain rating Scale (NPRS)8th weekThe NPRS is a commonly used, valid, flexible, and reliable outcome measure of pain. It consists of an 11-point rating system that takes a number between 0 and 10, where 0 means "no pain" and 10 means "worst imaginable pain." Patients are asked to select the value from scale that best represents their degree of pain.
Short Form Health survey (SF-36)8th weekShort Form Health survey (SF-36) is a self-reported health outcome measuring tool. There are 36 questions total, covering eight different health domains.
Spine Bridge test (SUBT)8th weekThe supine bridge test is the most frequently recommended test for evaluating the core muscles. Starting with a supine posture, each participant placed their feet on a bed near to but without touching one another. and both knees flexed 90 degrees. Next to the torso were the arms. With the shoulders, hips, and knees all in a straight alignment, the individual raised their pelvis off the bed. The test posture was maintained until it was no longer possible due to discomfort. If the participant completed two minutes in the test posture, one support point was removed and the dominant limb was extended in air.

Countries

Pakistan

Contacts

CONTACTimran amjad
imran.amjad@riphah.edu.pk03324390125
PRINCIPAL_INVESTIGATORhina G gul, PhD*

Riphah International University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 9, 2026