ClinicalTrials.gg
RecruitingNCT07576244Updated Sep 24, 2026

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

An interventional study of CORE STABILIZATION EXERCISES and MYOFASCIAL INDUCTION THERAPY in Low Back Pain, sponsored by Riphah International University. Recruiting at 1 site in Pakistan. Open to female participants aged 20 Years to 45 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-24.

Sponsored by Riphah International University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 7 months after the study started (first participant enrolled Oct 2025, registered May 2026).
  • Started Oct 2025; still recruiting 1 year 1 month later.
Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
20 Years to 45 Years
Sex
Female
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 118 studies in Low Back Pain by Riphah International University — 33 open to participants now, 34 under way, none of them phase 3. Low Back Pain · Riphah International University.

Planned enrollment
51st of 112
40 · median 40
Started
2025
with 21 others
No phase
112 of 118
32 open now
Primary completion
2026-10
later than 28 of 33 live
Registered
110th of 118
by date

Among the 118 studies in Low Back Pain by Riphah International University, this one is the 51st largest by planned enrollment of the 112 interventional ones, is one of 22 that started in 2025, is one of 112 with no phase, reaches primary completion later than 28 of the 33 other live ones, and was the 110th registered.

By phase

118 studies; the count open now beside each. This study's row is marked.

No phasethis study112 · 32 open
Observational6 · 1 open

By the year they started

First in 2018; this study’s year is marked. 22 started in 2025.

Size and results

Median enrollment 40 across the 112 interventional studies, 140 across the 6 observational. Of the 75 that completed or were terminated, 0 (0%) have results posted.

Was this useful?
Watch this landscapeDownload CSVWith an account: a weekly mail of what changed among 118 studies in Low Back Pain by Riphah International University, or all of them as a file.
02

Study 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.

Read the 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.

03

Conditions studied

  • Low Back Pain

Keywords

  • Exercises
  • Low-back pain
  • Postpartum
  • Quality of life
  • Induction therapy
04

Who can participate

Ages eligible
20 Years to 45 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

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

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

Exclusion criteria

Exclusion Criteria:

  • Spinal fracture or deformity
  • Arthritis
  • Lumber radiculopathy
  • Inflammatory condition that cause low back pain
  • Severe discopathy
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

05

Study design

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

Study arms

  • Experimental
    CORE STABILIZATION EXERCISES & MYOFASCIAL INDUCTION THERAPY

    Core stabilization exercises include bird-dog, side bridges, Curl ups and supine extension bridge. The Myofascial Induction therapy techniques related to the lumbopelvic region contain stroke application, deep induction application, cross-hands induction of the lumbar spine, and hip-flexor region induction.

    Other: CORE STABILIZATION EXERCISES · Other: MYOFASCIAL INDUCTION THERAPY

  • Active comparator
    CORE STABILIZATION EXERCISES

    Core stabilization exercises include bird-dog, side bridges, Curl ups and supine extension bridge.

    Other: CORE STABILIZATION EXERCISES

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

  • OtherMYOFASCIAL INDUCTION THERAPY

    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

06

What researchers measure

Primary outcomes

  1. Numeric Pain rating Scale (NPRS)

    The 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.

    Time frame: 8th week

  2. Short Form Health survey (SF-36)

    Short Form Health survey (SF-36) is a self-reported health outcome measuring tool. There are 36 questions total, covering eight different health domains.

    Time frame: 8th week

  3. Spine Bridge test (SUBT)

    The 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.

    Time frame: 8th week

07

Study locations

1 of 1 sites recruiting
08

References and documents

Publications

  • Abdelhaleem MD, Aly SM, Taha TS, Abdallah EA. Effect of 8 weeks of cognitive behavioral therapy versus 8 weeks core stabilization training in the management of subjects with non-specific low back pain: a randomized controlled trial. Bulletin of Faculty of Physical Therapy. 2024;29(1):37.
  • Smrcina Z, Woelfel S, Burcal C. A Systematic Review of the Effectiveness of Core Stability Exercises in Patients with Non-Specific Low Back Pain. Int J Sports Phys Ther. 2022 Aug 1;17(5):766-774. doi: 10.26603/001c.37251. eCollection 2022. PubMed 35949382 ↗
  • Prem L, Noman A, Muneeba A, Saifullah Khan D, Ghulam F, Ahmed Shahid A. Myofascial Release and Core Stability Exercises Among Chronic Lower Back Pain Patients: MFR and CSE for Chronic LBP. Journal of Health and Rehabilitation Research. 2024;4(3):1-5.
  • Gadre ST, Kanase SB, Mane D. Effect of core strengthening exercises on post-partum women with lumbar dysfunction. J Coast Life Med. 2022;10:210-9.
  • Mamipour H, Farazmehr S, Negahban H, Nazary-Moghadam S, Dehghan-Manshadi F, Navi Nezhad M, Jafari S, Sharifzadeh M. Effect of Core Stabilization Exercises on Pain, Functional Disability, and Quality of Life in Pregnant Women With Lumbar and Pelvic Girdle Pain: A Randomized Controlled Trial. J Manipulative Physiol Ther. 2023 Jan;46(1):27-36. doi: 10.1016/j.jmpt.2023.05.005. Epub 2023 Jul 7. PubMed 37422748 ↗

Individual participant data

Plan to share: No

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Oct 2025 (actual). Primary completion is estimated for Oct 2026, 12 months after the start.

Of 1,231 non-industry interventional studies with no phase under Low Back Pain, half reached primary completion within 11 months of starting (the median), counting those still running; a quarter within 5 and three quarters within 26. This study's planned 12 months is close to that.

Counting every sponsor, half of 1,286 studies reached it within 11 months; a quarter within 5 and three quarters within 27.

How these figures are worked out, and which studies are left out of them.

Registered
May 4, 2026
First posted
May 8, 2026
StartActual
Oct 1, 2025
Primary completionEst.
Oct 2026
CompletionEst.
Oct 2026
Last update
Sep 24, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 24, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07576244
Responsible party
Sponsor
First posted
May 8, 2026
Start date
Oct 1, 2025
Primary completion
Oct 2026 (estimated)
Completion
Oct 2026 (estimated)
Last update
Sep 24, 2026

Study contacts

imran amjad
Contact
imran.amjad@riphah.edu.pk
03324390125
hina G gul, PhD*
principal investigator · Riphah International University

Oversight

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

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

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