About this trial
This study aimed to evaluate the effectiveness of adding oculomotor techniques and hands-on treatments to routine exercise protocols for individuals with non-specific chronic neck pain (NSCNP).
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
The inclusion criteria included being between ages 18 and 65 old, having been diagnosed with nonspecific neck pain, being able to comply with exercise instructions and understand evaluation questions, and volunteering to participate in the research.
Disqualifiers
None
Trial design
Parallel
Treatments tested in this trial
Exercise
Other interventionIndividuals were randomly assigned to the REP (Routine Exercise Program) group and the OHP group. The REP group received the traditional exercise protocol and the OHP group received oculomotor exercises and myofascial release techniques in addition to the traditional exercise. The groups were evaluated before the treatment and at the end of the 6-week treatment sessions. Patient education was given to the patients before both programs. Patient education included information about nonspecific chronic neck pain, symptoms, and complications, as well as assessment methods, parameters, tests, and exercises. The first group, the REP group (n=19), received routine exercises, and the second group, the OHP group (n=19), received oculomotor exercises and myofascial relaxation techniques in addition to the routine exercise program. The treatments were applied for six weeks, three sessions per week, under the supervision and guidance of a physiotherapist in the clinic.
Treatment groups
Trial outcomes
Primary outcomes
Pain intensity
Pain intensity was measured with a visual analog scale (VAS).
Secondary outcomes
Proprioception
joint position sense (JPS) was assessed using a laser pointer.
Sponsors and contacts
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