Trial · NCT07908693
A Novel Treatment for Chronic Low Back Pain Using Multi Angular Isometric Lumbar Exercise: Randomized Clinical Trial.
NCT07908693, Not applicable, Recruiting, Hamad Medical Corporation
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. A Novel Treatment for Chronic Low Back Pain Using Multi Angular Isometric Lumbar Exercise: Randomized Clinical Trial. Trials, record NCT07908693. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07908693
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- A Novel Treatment for Chronic Low Back Pain Using Multi Angular Isometric Lumbar Exercise: Randomized Clinical Trial.
- NCT number
- NCT07908693
- Status
- Recruiting
- Phases
- Not applicable
- Enrollment
- 98 participants, estimated
- Lead sponsor
- Hamad Medical Corporation
- Conditions
- Nonspecific Low Back Pain, Low Back Pain, Chronic Low-back Pain (cLBP)
- Interventions
- MAILE (Multi Angular Isometric Exercise)
- First posted
- 2026-11-02
- Last updated
- 2026-11-02
Source ClinicalTrials.gov
Registered outcomes4
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Visual Analogue Scale (VAS) | Baseline assessment before intervention, midpoint assessment after 2 treatment sessions, and final assessment after completion of 6 sessions over a total intervention period of 3 weeks. | Pain Intensity measured using Visual Analogue Scale (VAS) |
| Secondary | Oswestry Disability Index (ODI) | Baseline assessment before intervention, midpoint assessment after 2 treatment sessions, and final assessment after completion of 6 sessions over a total intervention period of 3 weeks. | Measured using the Oswestry Disability Index (ODI) to evaluate how low back pain affects daily activities and overall function. |
| Secondary | Functional Stability (Core Stability) | Baseline assessment before intervention, midpoint assessment after 2 treatment sessions, and final assessment after completion of 6 sessions over a total intervention period of 3 weeks. | Assessed using: Single Leg Balance Test Single Leg Squat Test Three-Plane Core Test These tests evaluate lumbo-pelvic-hip stability and movement control. |
| Secondary | Lumbar Muscle Strength / Transversus Abdominis Activation | Baseline assessment before intervention, midpoint assessment after 2 treatment sessions, and final assessment after completion of 6 sessions over a total intervention period of 3 weeks. | Measured using the Pressure Biofeedback Unit (PBU) during the abdominal drawing-in maneuver (ADIM) to assess deep core muscle activation and control. |
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.
Papers14
The papers the trial lists on ClinicalTrials.gov.
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/NCT07908693
GET https://conductscience.org/api/trials/v1/NCT07908693/registered