Trial · NCT07887698
Effects of Instrument-Assisted Soft Tissue Mobilization Versus Post Facilitation Stretch Technique in Chronic Neck Pain
NCT07887698, Not applicable, Recruiting, Foundation University Islamabad
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Effects of Instrument-Assisted Soft Tissue Mobilization Versus Post Facilitation Stretch Technique in Chronic Neck Pain. Trials, record NCT07887698. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07887698
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Effects of Instrument-Assisted Soft Tissue Mobilization Versus Post Facilitation Stretch Technique in Chronic Neck Pain
- NCT number
- NCT07887698
- Status
- Recruiting
- Phases
- Not applicable
- Enrollment
- 38 participants, estimated
- Lead sponsor
- Foundation University Islamabad
- Conditions
- Cerival Pain, Chronic Neck Pain
- Interventions
- Instrument Assisted Soft Tissue Mobilization, Post Facilitation Stretch
- First posted
- 2026-10-21
- Last updated
- 2026-10-21
Source ClinicalTrials.gov
Registered outcomes3
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Neck Pain | Baseline and after 2 weeks | Pain intensity will be the primary outcome of this study and will be assessed using the Numeric Pain Rating Scale (NPRS). The NPRS is an 11-point self-reported scale ranging from 0 to 10, where 0 indicates no pain and 10 represents the worst imaginable pain. |
| Primary | Cerical Range of motion | Baseline and after 2 weeks | Cervical range of motion (ROM) will be the second primary outcome of this study and will be assessed using the Cervical Range of Motion (CROM) instrument. The CROM device is a valid, reliable, and clinically accepted tool designed to measure active cervical movements, including flexion, extension, right and left lateral flexion, and right and left rotation. It provides objective and precise measurements in degrees, allowing accurate evaluation of cervical mobility. |
| Primary | Neck Disability | Baseline and after 2 weeks | Neck disability will be the primary outcome of this study and will be assessed using the Neck Disability Index (NDI). The NDI is a valid, reliable, and widely used self-administered questionnaire that evaluates the impact of neck pain on functional activities and daily living. It consists of 10 items assessing pain intensity, personal care, lifting, reading, headaches, concentration, work, driving, sleeping, and recreation, with each item scored from 0 to 5. The total score ranges from 0 to 50, with higher scores indicating 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.
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/NCT07887698
GET https://conductscience.org/api/trials/v1/NCT07887698/registered