Trial · NCT07907458
Digital Use, 24-Hour Movement Behaviors, and Myofascial Release in University Students With Neck Pain
NCT07907458, Not applicable, Not yet recruiting, Karabuk University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Digital Use, 24-Hour Movement Behaviors, and Myofascial Release in University Students With Neck Pain. Trials, record NCT07907458. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07907458
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Digital Use, 24-Hour Movement Behaviors, and Myofascial Release in University Students With Neck Pain
- NCT number
- NCT07907458
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 56 participants, estimated
- Lead sponsor
- Karabuk University
- Conditions
- Forward Head Posture, Chronic Nonspecific Neck Pain
- Interventions
- Integrated Myofascial Release, Light-Touch Control
- First posted
- 2026-10-30
- Last updated
- 2026-10-30
Source ClinicalTrials.gov
Registered outcomes8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change in Pressure Pain Threshold | Baseline and immediately after six sessions (2 weeks) | Pressure pain threshold measured with a digital algometer with a 1 cm2 probe at standardized cervical muscle sites. Repeated measurements at each site are averaged and reported in kPa. A higher threshold indicates lower mechanical pain sensitivity. The primary comparison is baseline to completion of six sessions. |
| Secondary | Change in Craniovertebral Angle | Baseline, immediately after six sessions (2 weeks), and 1 month after treatment (approximately week 6), where feasible | Craniovertebral angle in degrees measured by standardized lateral photogrammetry using the tragus and C7. A larger angle indicates less forward head posture. Assessed at the start, 10 minutes, and 20 minutes of a standardized smartphone task. |
| Secondary | Change in Neck Pain Intensity | Baseline, immediately after six sessions (2 weeks), and 1 month after treatment (approximately week 6), where feasible | Average neck pain over the preceding week measured using a 0-10 Numerical Rating Scale, where 0 means no pain and 10 means the worst imaginable pain. Lower scores indicate less pain. |
| Secondary | Change in Cervical Range of Motion | Baseline, immediately after six sessions (2 weeks), and 1 month after treatment (approximately week 6), where feasible | Active cervical flexion, extension, right and left rotation, and right and left lateral flexion measured in degrees using a clinical range-of-motion device or digital inclinometer. Each direction is analyzed separately. |
| Secondary | Change in Neck Disability Index | Baseline, immediately after six sessions (2 weeks), and 1 month after treatment (approximately week 6), where feasible | Turkish Neck Disability Index: 10 items, each scored 0-5; total 0-50. Higher scores indicate greater neck-related disability. |
| Secondary | Change in Body Awareness | Baseline, immediately after six sessions (2 weeks), and 1 month after treatment (approximately week 6), where feasible | Turkish Body Awareness Questionnaire assesses awareness of bodily processes and responses. Eighteen items rated 1-7 yield a total of 18-126, with higher scores indicating greater body awareness. |
| Secondary | Change in Neck Awareness | Baseline, immediately after six sessions (2 weeks), and 1 month after treatment (approximately week 6), where feasible | Turkish Fremantle Neck Awareness Questionnaire: nine items scored 0-4, total 0-36. Higher scores indicate greater disturbance of neck-related perception. |
| Secondary | Pressure Pain Threshold at Follow-up | Baseline and 1 month after completion of treatment (approximately week 6), where feasible | Digital algometry at the same standardized cervical sites used at baseline, with repeated measurements averaged and reported in kPa; higher values indicate lower mechanical pain sensitivity. |
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/NCT07907458
GET https://conductscience.org/api/trials/v1/NCT07907458/registered