Chronic Pain Clinical Trial
— OsteoMAPOfficial title:
Stage 2 Delivery and Evaluation of an Integrated Osteopathy, Mindfulness and Acceptance-based Programme for Patients With Persistent Pain
Verified date | May 2017 |
Source | The British School of Osteopathy |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The purpose of this pre and post intervention observational study is to evaluate
patient-reported outcomes from an new clinical course which integrates Mindfulness and
Acceptance-based approaches from '3rd wave' Cognitive Behavioural Therapy with osteopathic
manual therapy treatment for patients with persistent pain.
It is being conducted by the British School of Osteopathy (BSO) in London. In Stage 1 (in
progress, June 2013 to August 2014), a course was developed for self-referring patients
attending the BSO Clinic. In Stage 2 (September 2014 to May 2016), delivery will be expanded
to evaluate outcomes for patients attending National Health Service (NHS) General
Practitioner (GP) surgeries in South East London.
The intervention consists of a pre-course screening interview; a structured course of six,
weekly, one-hour treatment sessions for individual patients; and an optional follow-up
interview after three months.
The evaluation study is being conducted by an independent study team from the National
Council for Osteopathic Research. Patients complete a set of standardised questionnaires
before the course and after six months to assess self-reported changes in quality of life,
well-being, activity levels, mindfulness and use of health resources. A sample of patients
will be invited to provide consent for a treatment session to be observed and/or recorded,
or to attend a follow-up interview after six months, to evaluate the quality of course
delivery. This is an observational study of patient-reported outcomes from a new
intervention in a single cohort of patients, so there is no formal study hypothesis but it
is anticipated that outcomes will include increased quality of life, well-being, and active
engagement with valued activities.
Status | Completed |
Enrollment | 255 |
Est. completion date | January 2017 |
Est. primary completion date | January 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Adults over the age of 18 - Persistent musculoskeletal pain for more than six months duration - Known medical diagnosis and stable condition - Pain or pain-related behaviour limits activity - Can identify scope for change - Motivated to participate in a six week, experiential self-management course - Suitable for osteopathic manual therapy - Able to provide informed consent - Sufficient spoken English to participate in consultations without an interpreter - Able to attend the selected clinic locations when appointments are available Exclusion Criteria: - Do not conform to the inclusion criteria above - Active, uncontrolled alcohol or substance abuse - Active uncontrolled psychotic mental health problem - Undergoing or awaiting further diagnostic medical investigations - Currently attending a pain clinic or other psychological support service |
Country | Name | City | State |
---|---|---|---|
United Kingdom | Iveagh House Surgery | London | |
United Kingdom | Stockwell Group Practice | London | |
United Kingdom | The British School of Osteopathy Clinical Centre | London |
Lead Sponsor | Collaborator |
---|---|
The British School of Osteopathy |
United Kingdom,
Abbey H & Nanke L. The development of a chronic pain self-management course within the British School of Osteopathy Clinic. International Journal of Osteopathic Medicine 16: e5-e6, 2013.
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | European Quality of Life Questionnaire (EQ5D) | To assess changes in quality of life from before the start of the six week course to six months after the course ends. | Pre-course baseline at week 0 to 30 weeks | |
Secondary | Activity Avoidance Questionnaire (AAQ-IIR) Questionnaire | To assess changes in activity levels from before the six week course starts to six months after the course ends. | Pre-course week 0 to week 30 | |
Secondary | Freiburg Mindfulness Inventory for mindfulness skills | To assess changes in mindfulness skills from before the start of the six week course to six months after the course ends | Pre-course week 0 to week 30 | |
Secondary | Bournemouth Questionnaire for pain-related beliefs and behaviour | To assess changes in pain avoidance beliefs and behavioural responses from before the start of the six week course to six months after the course ends | Pre-course week 0 to week 30 | |
Secondary | Self-reported changes in health resource utilisation | To assess participants' reports of changes in use of pain medication, GP consultations, and other healthcare interventions in the six months following the course | Single measure at 30 weeks |
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