Validating a Clinical Prediction Rule to Guide Manual Therapy and Exercise for Neck Pain Relief
Part of paid clinical trials in Rochester, Minnesota.
- Sponsor
- Baylor University
- Study ID
- NCT06906107
- Status
- Recruiting
Conditions
- Cervicalgia
- Neck Pain Musculoskeletal
- Neck Pain Treatment
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 70 Years
- Healthy Volunteers
- Not accepted
Interventions
- Cervical Manipulation — PROCEDUREHigh velocity low amplitude thrust joint manipulation to the cervical spine facet joints
- Exercise — PROCEDURETherapeutic exercises to the cervical, thoracic, and scapular musculature
- Mobilization — PROCEDURELow velocity, low amplitude movements applied to the cervical spine facet joints (Grade I or II)
Study Details
Neck pain is a common issue that can lead to long-term disability and lost work time for many individuals. Despite numerous studies, finding effective treatment strategies has been challenging. One possible reason for this is that treatments may not have been tested on the specific groups of people who would benefit most. A method was developed to identify people with neck pain who are likely to see significant improvements from a manipulation technique used by physical therapists, called cervical spine thrust joint manipulation. The investigators believe that patients identified as likely responders to cervical spine manipulation will show greater improvements in disability. The investigators aim to test whether this method works with different patients and therapists across the country through a multicenter randomized clinical trial. In this study, 160 patients with primary complaints of neck pain will be enrolled from 9 clinical sites. Designed with stringent criteria for inclusion, this study is a testament to our commitment to participant safety and the effectiveness of the treatment. Participants will be randomly assigned to one of two groups: (1) one group will receive 2 sessions of cervical spine manipulation followed by 3 sessions of exercise, and (2) the other group will receive 2 sessions of gentle hands-on treatment followed by 3 sessions of exercise. The primary goal is to measure changes in disability 4 weeks after starting treatment, with follow-ups after one week, 4 weeks, 3 months, and 6 months to assess both immediate and long-term effects. By providing crucial data on the reliability of our method in identifying patients who will benefit most from cervical spine manipulation, this study has the potential to significantly enhance decision-making leading to rapid improvement. Results from this study will provide clearer guidelines on the optimal use of cervical spine manipulation, potentially revolutionizing the way patients recover from neck pain.
Key Dates
- Start date
- Jun 1, 2025
- Status verified
- Apr 2026
- Primary completion
- Dec 31, 2026
- Completion
- Dec 31, 2026
Study Design
- Enrollment
- 160 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Cervical ManipulationPatients will receive cervical manipulation on 2 visits, followed by 3 visits of therapeutic exercise.
- Other: Exercise and MobilizationsPatients will receive low-grade cervical mobilizations on 2 visits, followed by 3 visits of therapeutic exercises
Primary Outcome Measure
Neck Disability Index [ Time Frame: 6 months ]
Central Contacts
- Jessica T Feda, DSc5079906446
- Tiffany L Barrett, DSc702-321-2144
Locations (4)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| ActivePT | Rochester | Minnesota | 55901 | |
| PROActivePT | Syracuse | New York | 13201 | |
| ActiveTherapy Alliance | Waco | Texas | 76798 | |
| Emplify by Bellin Health Ashwaubenon | Green Bay | Wisconsin | 54313 |
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