Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
Healthy Volunteers
ID06069362

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

Led by University of Deusto · Updated on 2025-03-26

91

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

U

University of Deusto

Lead Sponsor

U

University of the Basque Country (UPV/EHU)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are studying patients with nerve-related neck and arm pain, known as cervicobrachial pain, to find out which characteristics predict better response to physiotherapy. The main goal is to identify if a subgroup of patients responds better to manual physiotherapy treatment. This interventional study is sponsored by the University of Deusto and aims to evaluate how somatosensory profiles relate to treatment outcomes. Participants will undergo assessments including sensory testing, questionnaires about pain and disability, and clinical tests of neck movement and nerve sensitivity. The treatment involves six weekly sessions of manual physiotherapy focusing on gentle mobilisation techniques around the nerve root area, combined with home exercises to improve nerve mobility and cervical movement. After completing the treatment, initial measurements and a global rating of change scale will be repeated to determine treatment response. During the study, participants will provide demographic and clinical data, complete various questionnaires and sensory tests before and after treatment, and allow access to their imaging tests. Researchers will measure outcomes such as pain levels, disability, nerve sensitivity, and psychosocial factors at baseline, after six weeks, and at 14 weeks. The total study involvement includes initial assessment, six weeks of treatment, and follow-up evaluations to monitor changes and treatment effects.

CONDITIONS

Brief Title

Predictors of Response to Manual Physiotherapy Using Somatosensory Profiles in Patients With Cervicobrachial Pain

Who Can Participate

Age: 18Years - 80Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Subjects with unilateral cervicobrachial pain
  • Age between 18 and 80 years
Not Eligible

You will not qualify if you...

  • Signs of severe disease such as cervical myelopathy, tumor, rheumatic diseases, or central neurological pathology
  • Cervicobrachial pain caused by trauma or whiplash
  • Previous surgical intervention of the cervical spine

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 6 weeks

Participants receive manual physiotherapy including cervical passive mobilisation techniques and home neurodynamic exercises to reduce nervous system irritability.

Weekly visits for up to 6 weeks

Follow-up

Duration - Up to 8 weeks after treatment ends

After treatment completion, participants repeat initial assessments and complete a global rating of change to evaluate response to therapy.

1 follow-up visit at week 14

Trial Site Locations

Total: 1 location

1

University of Deusto

San Sebastián, Gipuzkoa, Spain, 20012

Actively Recruiting

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Research Team

X

Xabat Casado, PhD Cand

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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Published Research Related To This Trial