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 — PROCEDURE
    High velocity low amplitude thrust joint manipulation to the cervical spine facet joints
  • Exercise — PROCEDURE
    Therapeutic exercises to the cervical, thoracic, and scapular musculature
  • Mobilization — PROCEDURE
    Low 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 Manipulation
    Patients will receive cervical manipulation on 2 visits, followed by 3 visits of therapeutic exercise.
  • Other: Exercise and Mobilizations
    Patients 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

Locations (4)

FacilityCityStateZIPSite coordinators
ActivePTRochesterMinnesota55901
Jessica Feda, DSc
5079906446
Jake Hoeppner, DPT
507-322-3460
PROActivePTSyracuseNew York13201
Kyle R Adams, DSc
315-807-8160
Dan Gridley, DPT
315-458-2552
ActiveTherapy AllianceWacoTexas76798
Tiffany Barrett, DSc
254-457-8654
Erika Sutton, DPT
254-300-1941
Emplify by Bellin Health AshwaubenonGreen BayWisconsin54313
Jessica Feda Principal Investigator, DPT, DScPT
507-990-6446
Joe Kucksdorf Physical Therapy Supervisor - Emplify, DPT, DScPT
920-433-6757

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