Trial · NCT07892040
Comparative Effects of Exercises on Pain, Cervical Proprioception, Neck Disability and Visual Performance in Patients With Computer Vision Syndrome.
NCT07892040, Not applicable, Not yet recruiting, University of Management and Technology Lahore
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Comparative Effects of Exercises on Pain, Cervical Proprioception, Neck Disability and Visual Performance in Patients With Computer Vision Syndrome. Trials, record NCT07892040. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07892040
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Comparative Effects of Exercises on Pain, Cervical Proprioception, Neck Disability and Visual Performance in Patients With Computer Vision Syndrome.
- NCT number
- NCT07892040
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 46 participants, estimated
- Lead sponsor
- University of Management and Technology Lahore
- Conditions
- Computer Vision Syndrome
- Interventions
- Cervical Sensorimotor Training, Occulomotor Training
- First posted
- 2026-10-23
- Last updated
- 2026-10-23
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 post treatment | Numeric Rating Scale (NPRS) is most frequently used instruments to measure pain intensity .The 11-point numeric with 0 representing No pain, 1-3 representing Mild Pain (nagging, annoying, interfering little with ADLs), 4-6 representing Moderate Pains (interferes significantly with ADLs), 7-10 representing Sever Pain (disabling, unable to perform ADLs). |
| Primary | Neck Disability Index | Baseline and after 6 weeks post treatment | The NDI is a self-reported questionnaire that checks how much neck pain impacts daily life. It covers 10 areas (like pain, self-care, work, and recreation), each scored from 0 to 5. A higher total (out of 50) means more disability: * 0-4: No disability * 5-14: Mild * 15-24: Moderate * 25-34: Severe Above 34: Complete disability The NDI is a reliable way to assess neck-related issues. |
| Primary | Cervical Joint Position Error Test (JPE) | Baseline and after 6 weeks post treatment | This test measures neck proprioception (body awareness). A laser pointer on the head tracks how close someone can return to their starting position after moving their head with eyes closed. The closer they get, the better their proprioception. A difference over 4.5° suggests impaired awareness. The JPE test is dependable for checking neck movement sense |
| Primary | Visual Complaint Index (VCI) | Baseline and after 6 weeks post treatment | The VCI is a questionnaire that asks about vision problems like eye strain, blurred or double vision, headaches, sensitivity to light, and fatigue-especially from screen use or neck problems. Each symptom is rated for how bad and how often it is. Multiply those scores for each symptom and add them up for a total. Higher totals mean more symptoms. The VCI helps spot issues linked to Computer Vision Syndrome and neck-related visual problems |
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/NCT07892040
GET https://conductscience.org/api/trials/v1/NCT07892040/registered