Clinical trial Recruiting at 1 site Interventional Ages 18 to 80

Identifying predictors for effective physiotherapy in neck and arm pain patients

Official title: Prediction of Response to Manual Physiotherapy Using Somatosensory Profiles in Patients With Cervicobrachial Pain

Run by University of Deusto · NCT06069362 · Data updated 2026-11-12

This study is testing whether certain traits can help predict which patients with neck and arm pain will benefit most from manual physiotherapy and nerve exercises.

Quick facts

Study typeInterventional
Ages18 Years to 80 Years
SexAll
Enrollment91 (estimated)
SponsorUniversity of Deusto
Academic / other
Locations1 site (San Sebastián, Gipuzkoa)
StatusRecruiting
StartedApril 20, 2023
Main results expectedJuly 20, 2025
Study endsJuly 20, 2025
Registry record updatedMarch 26, 2025
Trial IDNCT06069362 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are individuals experiencing unilateral cervicobrachial pain without severe underlying conditions.

Probably not a fit

Patients with severe diseases, cervical myelopathy, or those who have had previous cervical spine surgery may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial aims to identify characteristics that predict how well patients with cervicobrachial pain respond to manual physiotherapy. Participants will undergo a thorough assessment of their clinical and neurophysiological profiles before receiving six sessions of manual physiotherapy and home nerve gliding exercises. The study will evaluate changes in symptoms and functionality after treatment, using various clinical tests and questionnaires to gather comprehensive data on their condition. The goal is to determine if specific subgroups of patients benefit more from this treatment approach.

Why it matters

Potential benefit: If successful, this study could lead to more personalized and effective physiotherapy treatments for patients with cervicobrachial pain.

How similar studies have gone: Similar studies have shown promise in identifying predictors of treatment response, suggesting this approach may yield valuable insights.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Subjects with unilateral cervicobrachial pain

Exclusion Criteria:

* Signs of severe disease, cervical myelopathy, tumour, rheumatic diseases or a neurological pathology of central origin.
* Cervicobrachial pain of traumatic origin or as a result of whiplash.
* Previous surgical intervention of the cervical spine.

Where it's running

  • University of Deusto
    San Sebastián, Gipuzkoa, Spain
    Recruiting

Study contacts

  • Principal investigator: Xabat Casado, PhD cand — University of Deusto
  • Study coordinator: Xabat Casado, PhD Cand
  • Email: xabat.casado@deusto.es
  • Phone: 943326600

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.