Physiotherapy Post Lumbar Discectomy: Prospective Feasibility and Pilot Randomised Controlled Trial
Alison Rushton1, Nicola R Heneghan1, Melanie Calvert2
1School of Sport, Exercise and Rehabilitation Sciences, College of Life and Environmental Sciences, University of Birmingham, Birmingham, United Kingdom.
This pilot study found physiotherapy and patient leaflets acceptable for post-lumbar discectomy patients, showing a trend in reduced disability. Further trials are needed to confirm effectiveness and optimize design for spinal surgery recovery.
Area of Science:
- Orthopedics and Sports Medicine
- Rehabilitation Sciences
- Clinical Trial Methodology
Background:
- A pilot randomized controlled trial was conducted in UK secondary care settings.
- The study focused on patients over 18 years old following primary, single-level lumbar discectomy.
- Trial registration: ISRCTN registry 33808269.
Purpose of the Study:
- To assess the acceptability and feasibility of trial procedures for post-lumbar discectomy patients.
- To evaluate the score distribution of the Roland Morris Disability Questionnaire (RMDQ).
- To examine the efficient functioning of trial components for future research.
Main Methods:
- Participants were randomized 1:1 to receive either a patient leaflet alone or physiotherapy outpatient management plus a patient leaflet.
- Blinded assessments were performed at 4 weeks (baseline) and 12 weeks post-surgery.
- Secondary outcomes included pain, function, quality of life, and medication use.
Main Results:
- Recruitment achieved 54% of eligible consented patients, with 39% loss to follow-up at 12 weeks.
- Both groups showed a trend towards reduced RMDQ scores at 12 weeks, indicating no floor effect.
- Participant adherence was good, and no adverse events were reported.
Conclusions:
- Physiotherapy and patient leaflet interventions were acceptable and showed a promising trend in reducing disability.
- A larger, adequately powered randomized controlled trial with a different design is recommended.
- Findings will inform the design of future trials, potentially using the RMDQ as the primary outcome measure.
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