← Eichor
Study identifier: NCT06069362 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

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

Condition: Cervical Radicular Pain · Cervical Radiculopathy · Cervical Pain  ·  Sponsor: University of Deusto

PhaseNA
Planned participants91
Who can joinAll sexes, 18 Years to 80 Years
Healthy volunteersYes

About this study

The goal of this clinical trial is to investigate about the characteristics that predict response to physiotherapy treatment in patients with nerve related neck arm pain. The main question to answer is whether there is a subgroup that responds better to physiotherapy treatment. Participants will be assessed for clinical and neurophysiological characteristics prior to treatment. Afterwards they will receive 6 sessions of manual physiotherapy treatment along with home nerve gliding exercises once a week. Baseline measurements will be taken again after treatment to know if there have been any changes.

This description comes directly from the study's public registry record.

Talk to the study team

Xabat Casado, PhD Cand  ·  943326600  ·  xabat.casado@deusto.es

Always discuss trial participation with your own doctor first.

Locations (1)

University of DeustoSan Sebastián, Gipuzkoa, SpainRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06069362