MedPath

Observed Actions in Chronic Neck Pain

Not Applicable
Completed
Conditions
Chronic Pain
Registration Number
NCT02553759
Lead Sponsor
AG Clinic
Brief Summary

The aim of the present protocol is to prove if the observed actions (AOb) will improve the cervical range of motion (CROM) in patients with non-specific chronic neck pain (CNP). This study is a parallel-group double blind randomized clinical. Outcome measures were CROM, and pressure pain detection thresholds (PPDT) with a digital algometer. The follow-up will consist of three evaluations: pre- treatment, post-treatment and 10 minutes after second measurement (motor imagery).

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
28
Inclusion Criteria
  • Non specific chronic neck pain
  • Diagnosed by medical specialist
Exclusion Criteria
  • cervical osteoarthritis or polyarthrosis
  • rheumatic disease
  • history of cervical hernia
  • whiplash syndrome
  • surgery on the neck, face or shoulders,
  • systemic disease, medical history of cancer
  • significant trauma that the patient relates to their pain and/or refusal to participate

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Range of motion degrees10 minutes
Secondary Outcome Measures
NameTimeMethod

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.