4-week Mindfulness Program for Adults With Chronic Pain



Status:Completed
Conditions:Chronic Pain, Chronic Pain
Therapuetic Areas:Musculoskeletal
Healthy:No
Age Range:18 - Any
Updated:12/7/2018
Start Date:April 23, 2018
End Date:October 26, 2018

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Feasibility of a 4-week, Adapted Mindfulness Program for Adults With Chronic Pain

The objective of this study is to determine the feasibility and acceptability of a 4-week
mindfulness training program for adults with chronic pain (noncancer related). The
intervention is based on the MIndfulness-based Stress Reduction Program, an 8-week
mindfulness training program developed to help people manage stress-related and chronic
conditions. The adapted mindfulness intervention will consist of four, weekly 1 hour and 30
minute group sessions that are modified from the original program to fit the shorter length
and to directly address chronic pain management. Participants will complete pre- and
post-intervention surveys and daily mindfulness practice diaries, all online. The surveys
will help us determine if participants experience decreased pain interference, increased
quality-of-life, and increased psychological well-being over the course of the intervention.
Participants will also complete a post-intervention telephone interview to help determine
satisfaction with the intervention and areas where the intervention can be improved.


Inclusion Criteria:

- One or more chronic noncancer pain diagnoses (daily pain for at least 3 months)

- Has a pain management provider

- Reports more than minimal pain bothersomeness and interference in general activities

- Able to read and understand English

Exclusion Criteria:

- Diagnosis of mental illness with psychotic features

- History of inpatient admission for psychiatric disorder in past 2 years

- Active alcohol or substance abuse within the past year

- Has completed a mindfulness-based stress reduction or other mindfulness course; has or
previously had a regular mindfulness meditation practice.

- Unable or unwilling to comply with study procedures (online questionnaires and
practice diaries, 4 weekly intervention sessions, home practice, and one
semi-structured phone interview).
We found this trial at
1
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Chapel Hill, North Carolina 27599
(919) 962-2211
Phone: 919-445-6109
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