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Efficacy of a mindfulness-based intervention for spinal cord injured outpatients with chronic neuropathic pain

Efficacy of a mindfulness-based intervention for spinal cord injured outpatients with chronic neuropathic pain: a randomised controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN14165286
Enrollment
48
Registered
2014-12-02
Start date
2015-01-05
Completion date
Unknown
Last updated
2018-02-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Spinal Cord Injury: Chronic Pain

Interventions

For this research, all SCI patients who have been discharged from Stoke Mandeville Hospital within the last 20 years will be contacted. Of those who respond reporting chronic pain, 24 SCI participants

Sponsors

The University of Buckingham
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Participants with a spinal cord injury must be one year post-discharge from a spinal unit. 2. Each SCI participant must have a partner or primary caregiver willing to also take part. 3. All participants both male and female must be over 18 years of age and sufferers of chronic pain for three months or longer. There is no upper age limit. 4. Sufficient understanding of English must be held by all participants.

Exclusion criteria

Exclusion criteria: 1. Participants will not be recruited if they hold any cognitive impairment or mental illness. 2. Participants with articulation difficulties and an insufficient understanding of English will be excluded from this study. 3. Any respondents with any other long term health condition that may affect the experience of pain, or be the cause of chronic pain (as opposed to the spinal injury) will be excluded.

Design outcomes

Primary

MeasureTime frame
1. Quality of life 2. Depression 3. Anxiety Outcome measures will be assessed using online questionnaires, and will be measured at baseline, four weeks, eight weeks (or upon completion of the online course), and 20 weeks (or three months post-completion of the course).

Secondary

MeasureTime frame
1. Pain-related outcomes (catastrophising, pain intensity) 2. Social relationship measures.

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026