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Predictors of Response After Physiotherapy Treatment in People With Chronic Non-specific Neck Pain

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goal of this clinical trial is to investigate whether electroencephalographic features are associated with the multidimensional clinical characteristics of adults with chronic non-specific neck pain and whether clinical and brain function measures change following physiotherapy. Participants with chronic non-specific neck pain will receive six weekly treatment sessions consisting of a manual physiotherapy and neck-specific exercise programme, including a home exercise programme. Clinical, psychophysical, and 64-channel electroencephalographic assessments will be performed at baseline and approximately one week after completion of the intervention. Clinical outcomes will also be reassessed 12 weeks after the last treatment session. Electroencephalographic recordings will be obtained while participants are seated comfortably and instructed to remain relaxed. EEG-derived measures will be examined in relation to pain intensity, neck-related disability, psychological and cognitive-affective factors, sleep quality, and psychophysical pain responses. Healthy participants without chronic neck pain will undergo a comparable baseline assessment to provide reference data for the interpretation of brain function in the clinical group.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:

• Chronic non-specific neck pain (\>3 months duration)

• Willing and able to sign informed consent for study participation

Locations
Other Locations
Spain
Ander Cervantes Benítez
RECRUITING
San Sebastián
Time Frame
Start Date: 2024-03-21
Estimated Completion Date: 2027-12
Participants
Target number of participants: 100
Treatments
Experimental: Physiotherapy group
Participants with chronic non-specific neck pain will receive a 6-week physiotherapy intervention consisting of six individual treatment sessions, including manual therapy directed at the cervical and thoracic regions, together with a home exercise program. Clinical and brain activity assessments will be performed before the intervention and approximately one week after completion of the intervention.
No_intervention: Healthy control group
Healthy participants without chronic neck pain will undergo baseline clinical, psychophysical, and electroencephalographic assessments for comparison with participants with chronic non-specific neck pain. They will not receive the physiotherapy intervention or undergo a post-intervention assessment.
Related Therapeutic Areas
Sponsors
Leads: Ander Cervantes Benítez

This content was sourced from clinicaltrials.gov