header advert
Orthopaedic Proceedings Logo

Receive monthly Table of Contents alerts from Orthopaedic Proceedings

Comprehensive article alerts can be set up and managed through your account settings

View my account settings

Visit Orthopaedic Proceedings at:

Loading...

Loading...

Full Access

Spine

OSCAR (OSTEOPATHIC SINGLE CASE RESEARCH) – ASSESSING THE EFFECTS OF STANDARD AND BIOPSYCHOSOCIALLY INFORMED OSTEOPATHIC MANAGEMENT FOR PATIENTS WITH NON-SPECIFIC LOW BACK PAIN: PROTOCOL FOR A SINGLE CASE EXPERIMENTAL DESIGN (SCED)

The Society for Back Pain Research (SBPR) Annual General Meeting, ‘PANNING FOR GOLD’ 50+ Anniversary Meeting, Coventry, England, 30 June – 1 July 2022.



Abstract

Background

Osteopathy has been shown to be effective in the management of chronic low back pain. Guidelines recommend biopsychosocial care for chronic, complex musculoskeletal conditions, including non-specific low back pain but there is a lack of evidence comparing standard osteopathic care, which has traditionally been based on dated and disputed biomechanical theories of dysfunction, with more contemporary biopsychosocial approaches.

Methods and results

A multiple baseline single case experimental design trial with 11 UK osteopaths and 60 patients is currently assessing effectiveness of osteopathic treatment for patients with non-specific low back pain of more than 12 weeks’ duration. Patients are randomised to early, middle, or late treatment start dates to increase the validity of inferences about the effects of treatment. Osteopaths have participated in one course on the study protocol and processes pre-participation and will take an e-learning course on the biopsychosocial management of patients with low back pain after the first patient recruitment stage. Statistical analysis will assess the degree and rate of change between baseline, intervention and follow-up periods, and whether differences in effect are observed after the osteopaths have completed the biopsychosocial patient management training course. Primary outcomes will be the Numeric Pain Rating and Patient Specific Function Scales, measured daily at baseline and for 6 weeks during the intervention stage, and weekly or fortnightly during a 12-week follow-up period.

Conclusion

This experimental design will offer osteopaths in practice the opportunity to engage in research evaluating the effectiveness of osteopathic care and the influence of a training programme to augment biopsychosocial osteopathic care.

Study registration: https://clinicaltrials.gov/ct2/show/NCT05120921

Sources of funding: The Osteopathic Foundation

Conflict of interest: The authors declare no competing interests.

Previous publication of work: This protocol is under review with a peer-reviewed journal.


Email: