Entrapment Neuropathies: Challenging Common Beliefs With Novel Evidence.
Annina B Schmid, Louise Hailey, Brigitte Tampin
https://pubmed.ncbi.nlm.nih.gov/29385943Actively Recruiting
Led by University of Deusto · Updated on 2025-03-26
91
Participants Needed
1
Research Sites
N/A
Total Duration
U
University of Deusto
Lead Sponsor
U
University of the Basque Country (UPV/EHU)
Collaborating Sponsor
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
Predictors of Response to Manual Physiotherapy Using Somatosensory Profiles in Patients With Cervicobrachial Pain
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Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
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
Total: 1 location
1
University of Deusto
San Sebastián, Gipuzkoa, Spain, 20012
Actively Recruiting
X
Xabat Casado, PhD Cand
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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Annina B Schmid, Louise Hailey, Brigitte Tampin
https://pubmed.ncbi.nlm.nih.gov/29385943Nikolai Bogduk
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https://pubmed.ncbi.nlm.nih.gov/27586831