Trial · NCT07905391
McGill Stabilization Exercises Versus Pilates for Chronic Low Back Pain
NCT07905391, Not applicable, Not yet recruiting, University of Management and Technology Lahore
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. McGill Stabilization Exercises Versus Pilates for Chronic Low Back Pain. Trials, record NCT07905391. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07905391
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- McGill Stabilization Exercises Versus Pilates for Chronic Low Back Pain
- NCT number
- NCT07905391
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 40 participants, estimated
- Lead sponsor
- University of Management and Technology Lahore
- Conditions
- Chronic Non-Specific Low Back Pain
- Interventions
- McGill Stabilization Exercises, Pilates
- First posted
- 2026-10-29
- Last updated
- 2026-10-29
Source ClinicalTrials.gov
Registered outcomes4
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Numeric pain Rating Scale | Baseline and after 6 weeks | The 11-point Numeric Pain Rating Scale (NPRS) is a commonly used tool for assessing the intensity of pain. Participants are asked to rate their pain on a scale ranging from 0 to 10, where 0 indicates no pain and 10 represents the worst possible pain. Participants rate the intensity of pain experienced on the day of assessment. |
| Primary | Modified Modified Schober Test (MMST) | Baseline and after 6 weeks | The Modified Modified Schober Test (MMST) is a clinical measurement tool used to assess lumbar spine flexibility and mobility. The measurement is performed with the participant standing upright. The examiner palpates the lower border of the posterior superior iliac spines (PSIS), marks the identified point, and draws a horizontal line across the skin through both PSIS landmarks and the midline of the lumbar spine. A second horizontal mark is made 15 cm above the first mark using a measuring tape. The participant is then instructed to bend forward as far as comfortably possible, keeping the knees extended and avoiding painful movement. The examiner measures the distance between the two marks in the upright and forward-flexed positions. The difference between these measurements indicates lumbar flexion mobility, with a greater increase in distance suggesting greater lumbar flexibility. An increase of less than 5 cm is considered indicative of restricted lumbar mobility. |
| Primary | Modified Oswestry Disability Index | Baseline and after 6 weeks | Disability will be assessed using the Modified Oswestry Disability Index (MODI), a modified version of the original Oswestry Disability Index. In this version, the section on sexual activity is replaced with questions related to employment and homemaking abilities, as the sexual activity section is frequently left unanswered. The MODI score ranges from 0 to 100, with higher scores indicating greater disability. Scores are classified as minimal disability (0-20), moderate disability (21-40), severe disability (41-60), crippling disability (61-80), and bed-bound disability (81-100). |
| Primary | MSK Ultrasound | Baseline and after 6 weeks | Musculoskeletal ultrasonography will be used to assess transversus abdominis (TrA) muscle thickness using an ultrasound device equipped with a high-frequency linear array transducer (7.5-14 MHz). The probe will be positioned perpendicular to the muscle at the midpoint of the line connecting the iliac crest to the inferior angle of the last rib. Muscle thickness will be measured using a perpendicular caliper placed between the superficial and deep hyperechoic fascial borders. Three measurements will be obtained, and their average will be used for statistical analysis. |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07905391
GET https://conductscience.org/api/trials/v1/NCT07905391/registered