Sensorimotor disturbances in neck disorders affecting postural stability, head and eye movement control.
Julia Treleaven
https://pubmed.ncbi.nlm.nih.gov/17702636Actively Recruiting
Led by Universidad Miguel Hernandez de Elche · Updated on 2025-12-29
81
Participants Needed
1
Research Sites
N/A
Total Duration
Researchers are evaluating the effects of combining pain neuroscience education with therapeutic exercise for people experiencing non-specific neck pain. This study focuses on how this combination impacts pain levels, fear of movement (kinesiophobia), catastrophizing thoughts, understanding of exercise, and upper limb function. The trial also aims to compare the results of exercise alone versus exercise combined with tailored pain education in improving these outcomes. Participants will be randomly assigned to one of three groups: one receiving pain neuroscience education plus exercise, one receiving exercise alone, and a control group receiving a placebo intervention involving a turned-off TENS device. The education session lasts 20 minutes and focuses on movement-related fears and benefits of exercise. Exercise interventions include specific upper limb performance tests with increasing difficulty based on fatigue levels. The placebo group receives no exercise or education but undergoes the placebo procedure for 15 minutes. Throughout the study session, participants will complete several assessments including pain ratings, fear of movement, catastrophizing scales, beliefs about pain and exercise, and upper limb performance tests. Measurements are taken before intervention, after education or rest, and after exercise or placebo. These evaluations aim to understand changes in pain, psychological factors, and physical function. The study participation involves a single session with multiple assessments and interventions conducted under blinded conditions to reduce bias.
CONDITIONS
Effects of Education and Exercise on Pain, Psychosocial Factors, and Upper Limb Function in Non-specific Neck 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 - Single day session
Participants undergo baseline assessments including pain, psychosocial factors, and upper limb function tests. Depending on group assignment, participants receive either pain neuroscience education combined with therapeutic exercise, therapeutic exercise alone, or a placebo intervention with a turned-off TENS device. The exercise involves variations of upper limb performance tests adjusted to participant fatigue levels.
1 visit (in-person)
Total: 1 location
1
Clínica de Franscisco Ortega Rehabilitación Avanzada S.L.
Elche, Alicante, Spain, 03203
Actively Recruiting
J
Jaime Gascón-Jaén, Physiotherapist, MSc
M
Miguel Delicado-Miralles, PhD
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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