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RecruitingNCT06303401Updated Mar 12, 2024

Comparison of Thrust Manipulation of Sacroiliac Joint and Pelvic Stabilization Exercises in Post Partum Low Back Pain

An interventional study of SI joint thrust manipulation and pelvic stabilization exercises in Low Back Pain, Post Partum, sponsored by Riphah International University. Recruiting at 1 site in Pakistan. Open to female participants aged 20 Years to 40 Years. Per ClinicalTrials.gov, last updated 2024-03-12.

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

From the registry’s dates

  • Primary completion was expected by Jul 2024, 2 years 2 months ago, but the record still lists the study as recruiting.
  • Registered 5 months after the study started (first participant enrolled Sep 2023, registered Mar 2024).
  • Started Sep 2023; still recruiting 3 years later.
Phase
Not applicable
Study type
Interventional
Enrollment
44
Allocation
Randomized
Ages
20 Years to 40 Years
Sex
Female
01

Study summary

compare the effectiveness of SI joint thrust manipulation and pelvic stabilization exercises on Modified OSWESTRY Low Back pain Index (ODI) and Numeric Pain Rating Scale (NPRS) in patients with post-partum lower back pain.

Read the detailed description

Patients fulfilling the inclusion criteria will be divided into 2 groups i.e. Group A and Group B. Patients in Group A will receive thrust manipulation technique and Group B will receive pelvic stabilization exercises, heating pad will be given to both groups. Patients will be treated 3 times per week for 4 consecutive weeks. Patient will be evaluated at baseline, midline and at end of 4th week. Pain, functional status and disability will be evaluated after every 3 sessions.

02

Conditions studied

  • Low Back Pain, Post Partum
03

In context

Back Pain

2,373 studies on the registry are indexed under Back Pain; 284 are open to participants now.

This study's planned enrollment of 44 is below the median of 60 across 1,941 interventional studies indexed under Back Pain.

Browse Back Pain studies →

Lead sponsor

Riphah International University is the lead sponsor of 2,133 studies on the registry; 633 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

  • age 20-40 years
  • Postpartum women (after 6 weeks)(3, 12)
  • Postpartum LBP patient
  • Patient pain increased by provocation test i.e. Faber test, High thrust test and Gaenslen test

Exclusion criteria

Exclusion Criteria:

  • C-section
  • inflammatory or malignant type of pain
  • Neurological deficit
  • Severe trauma
  • Pelvic fracture
  • Osteoporosis, spinal stenosis, spondylolysis, spondoloesthesisi
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Investigator)
Enrollment
44 participants (estimated)

Study arms

  • Experimental
    SI joint thrust Manipulation

    The patient was supine and the therapist stood contralateral to the side which was to be manipulated. The patient was passively moved into side bending toward the side to be manipulated. The therapist passively rotated the patient, and then delivered a quick thrust to the Anterior Superior Iliac Spine (ASIS) in a posterior and inferior direction

    Other: SI joint thrust manipulation

  • Active comparator
    Pelvic Stabilization Exercises

    Heating pad for 10- 15 mints Pelvic stabilization exercises. Bridging (3 sets x 10 reps with 10 secs hold), Pelvic Tilt exercise (3 sets x 10 reps with 10 secs hold), Bird-Dog Exercise (3 sets x 10 reps with 10 secs hold), clamshell Exercise (3 sets x 10 reps with 10 secs hold).

    Other: pelvic stabilization exercises

Interventions

  • OtherSI joint thrust manipulation

    experimental group given the thrust manipulation along with heating pad. 3 sessions per week will be given for 4 weeks. The pain measure by using NPRS, functional status and disability through ODI will be evaluated. after every 3 sessions.

  • Otherpelvic stabilization exercises

    Heating pad for 10- 15 mints Pelvic stabilization exercises include Bridging (3 sets x 10 reps with 10 secs hold) Pelvic Tilt exercise(3 sets x 10 reps with 10 secs hold) Bird-Dog Exercise (3 sets x 10 reps with 10 secs hold) clamshell Exercise (3 sets x 10 reps with 10 secs hold) .3 sessions per week will be given for 4 weeks. The pain using NPRS , functional status and disability will be evaluated by using ODI after every 3 sessions.

06

What researchers measure

Primary outcomes

  1. Numeric pain rating scale (NPRS)

    The Numeric Pain Rating Scale (NPRS) measures the subjective intensity of pain. The NPRS is an eleven-point scale: the patient rates pain from 0 (no pain) to 10 (worst imaginable pain).

    Time frame: 4th week

  2. Modified Oswestry Disability Index (ODI)

    The ODI is a disease specific disability measure is used to establish a level of disability stage on a patient activity status and monitor change over the time. The ODI is made up of 10 questions. Each question is scored from (o-5) minimum to maximum.

    Time frame: 4th week

07

Study locations

1 of 1 sites recruiting
  • Lady Reading Hospital and Shahab Orthopedic & General Hospital
    Peshawar, KPK 25000, Pakistan
    • Asmar Fatima, MS OMPT · Contact · asmar.fatima@riphah.edu.pk · 03336195644
    • Gull alay, MS OMPT* · Principal investigator
    • Asmar Fatima, MS OMPT · Sub investigator
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 12, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06303401
Lead sponsor
Riphah International University
Responsible party
Sponsor
First posted
Mar 12, 2024
Start date
Sep 27, 2023
Primary completion
Jul 31, 2024 (estimated)
Completion
Aug 30, 2024 (estimated)
Last update
Mar 12, 2024

Study contacts

Imran Amjad, Phd
Contact
imran.amjad@riphah.edu.pk
03324390125
Asmar Fatima, MS OMPT
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 ↗

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