The Cervical "STRETCH" Study
Public ClinicalTrials.gov record NCT07440030. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
The Cervical "STRETCH" (Stretching Trials for Range, Ease, and Teaching Curriculum Health) Study
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
Neck pain and reduced cervical range of motion (ROM) are common musculoskeletal concerns that can significantly impact an individual's quality of life and daily routine. This is especially true for medical students who spend a disproportionate amount of time on their computers or mobile devices, as is required by their long study hours. A simple stretching routine is often recommended by physicians and physical therapists alike, but there is little research examining short-term changes in cervical range of motion (ROM) and pain when a brief, structured daily stretching program is used. The goal of this single-group study is to test feasibility and determine how well a daily cervical stretching regimen affects cervical ROM and self-reported pain in osteopathic medical students with cervical ROM restrictions. Researchers will measure changes in cervical ROM using a goniometer and changes in pain levels via the Visual Analog Scale (VAS). Participants will be asked to complete a 7-day period of no stretching, during which natural measurements will be taken, followed by 7 days of completing the 5-minute stretching routine, after which more measurements will be taken. Participants will also be asked to complete a post-study survey and a 1-month follow-up survey to provide feedback on the study and the stretching routine.
Study identification
- NCT ID
- NCT07440030
- Recruitment status
- Not yet recruiting
- Study type
- Interventional
- Phase
- Not applicable
- Enrollment
- 75 participants
Conditions and interventions
Conditions
Eligibility (public fields only)
- Age range
- 18 Years and older
- Sex
- All
- Healthy volunteers
- Accepts healthy volunteers
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Mar 9, 2026
- Primary completion
- May 31, 2026
- Completion
- Aug 29, 2026
- Last update posted
- Feb 26, 2026
2026
United States locations
- U.S. sites
- 1
- U.S. states
- 1
- U.S. cities
- 1
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Western University of Health Sciences | Pomona | California | 91767 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT07440030, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Feb 26, 2026 · Synced Sep 6, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT07440030 live on ClinicalTrials.gov.