Trial · NCT07894965
Dual-Task Core Stabilization Training in Chronic Nonspecific Low Back Pain
NCT07894965, Not applicable, Not yet recruiting, Karabuk University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Dual-Task Core Stabilization Training in Chronic Nonspecific Low Back Pain. Trials, record NCT07894965. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07894965
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Dual-Task Core Stabilization Training in Chronic Nonspecific Low Back Pain
- NCT number
- NCT07894965
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 90 participants, estimated
- Lead sponsor
- Karabuk University
- Conditions
- Chronic Nonspecific Low Back Pain
- Interventions
- Dual-Task Core Stabilization Exercise, Single-Task Core Stabilization Exercise
- First posted
- 2026-10-26
- Last updated
- 2026-11-03
Source ClinicalTrials.gov
Registered outcomes6
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Motor Dual-Task Cost During the Timed Up and Go Test | Baseline and post-intervention (approximately 6 weeks) | Motor dual-task cost will be calculated as \[(dual-task TUG time - single-task TUG time) / single-task TUG time\] × 100. TUG time will be measured in seconds. During the dual-task condition, participants will count backward by threes while performing the TUG test. Two trials per condition will be averaged. Higher percentages indicate greater deterioration in motor performance under dual-task conditions. The primary comparison will be the post-intervention value adjusted for baseline performance and age stratum. |
| Secondary | Cognitive Dual-Task Cost During the Timed Up and Go Test | Baseline, post-intervention (approximately 6 weeks), and 12-week follow-up. | Cognitive performance will be assessed by counting backward by threes under seated single-task and walking dual-task conditions. The correct response rate will be calculated as correct responses per second. Cognitive dual-task cost (%) = \[(single-task correct response rate - dual-task correct response rate) / single-task correct response rate\] × 100. Higher values indicate greater cognitive performance deterioration. |
| Secondary | Walking Speed During the 10-Meter Walk Test | Baseline, post-intervention (approximately 6 weeks), and 12-week follow-up. | Walking speed will be assessed under single-task and cognitive dual-task conditions on a 14-meter walkway, with the central 10 meters timed. During the dual-task condition, participants will count backward by threes. Two trials per condition will be averaged. Walking speed will be expressed in meters per second (m/s), with higher values indicating faster walking. |
| Secondary | Single-Leg Stance Test Performance | Baseline, post-intervention (approximately 6 weeks), and 12-week follow-up. | Static balance will be assessed on the preferred leg with arms crossed over the chest under three conditions: eyes open, eyes open with serial subtraction by threes, and eyes closed. Each trial will be limited to 45 seconds. The better result of two trials will be recorded for each condition. Performance will be expressed in seconds, with longer duration indicating better balance. |
| Secondary | Pain Intensity Measured by the Numerical Rating Scale | Baseline, post-intervention (approximately 6 weeks), and 12-week follow-up. | Average low back pain intensity during the previous week will be assessed using an 11-point Numerical Rating Scale (NRS), ranging from 0 (no pain) to 10 (worst imaginable pain). Higher scores indicate greater pain intensity. A reduction of at least 2 points or 30% will be considered clinically important. |
| Secondary | Disability Measured by the Oswestry Disability Index | Baseline, post-intervention (approximately 6 weeks), and 12-week follow-up. | Low back pain-related disability will be assessed using the validated Turkish version of the Oswestry Disability Index (ODI). Scores will be expressed as percentages from 0% (no disability) to 100% (maximum disability). Higher scores indicate greater disability. |
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.
Tests1
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as |
|---|---|
| Arithmetic Fluency Task | Secondary outcome |
Source ConductCognition
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/NCT07894965
GET https://conductscience.org/api/trials/v1/NCT07894965/registered