Rotator Cuff Injuries Clinical Trial
Official title:
A Pilot Randomized, Controlled Trial of the Effectiveness of Pain Neuroscience Education on Pain Intensity, Patients' Attitudes and Beliefs About Pain, Disability and Quality of Life After Arthroscopic Rotator Cuff Repair
The aim of this study was to evaluate the effects of a 8-week pain neuroscience education programme compared to a biomedical education programme on the rehabilitation of patients who undergo arthroscopic rotator cuff repair. Outcome measures included pain intensity, patients' attitudes and beliefs about pain, disability and quality of life.
This was a single-blinded, randomized parallel study. Twenty- nine patients who undergo
arthroscopic rotator cuff repair took part in a multimodal physiotherapy programme and were
allocated to two groups. Patients in the experimental group - PNE (n= 16) received multimodal
physiotherapy along with pain neuroscience education, and the control group- PME (n=13)
received multimodal physiotherapy along with biomedical education. The multimodal treatment
included 1-hour sessions 3 times per week for 8 weeks (24 sessions). In addition, the
education component (PNE, PME) consisted of 4 education sessions of 30 minutes duration, on a
one-to-one basis, once per week at the start of the programme.
Physiotherapists involved in the delivery of the interventions were previously trained on
both, the theoretical and practical aspects related to the protocols of multimodal
physiotherapy and specially on the education component.
Outcome measures included pain intensity (pain intensity numerical rating score),
catastrophizing, kinesiophobia, disability and quality of life.
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