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Pilot randomised controlled trial of a brief mindfulness-based intervention for those with persistent pain.

Journal of behavioral medicine
December 1, 2019
Ana Howarth et al. (9 authors)
Journal ArticleRandomized Controlled TrialHuman StudyClinical
Study Details

Study Goal

The researchers aimed to examine the effects of a brief mindfulness-based intervention (MBI) on persistent pain patients and assess the feasibility of conducting a definitive RCT.

Results Summary

The study found no significant immediate effects of the MBI but reported positive effects for intervention 'usefulness' at 1 week and pain self-efficacy at 1 month compared to the control group. Recruitment was feasible, but retention strategies were needed.

Population

Persistent pain patients

Effective Dosage

15-minute mindfulness body-scan audio, used independently over 1 month

Duration

1 month

Interactions

None mentioned

Extracted Claims (3)
InterventionDirectionEndpointPopulationDosageImpactClaim #
brief mindfulness-based intervention (MBI)
no change
pain severity, distraction and distress
persistent pain patients
no significant change
no significant immediate intervention effects
#1
brief mindfulness-based intervention (MBI)
increase
intervention 'usefulness'
persistent pain patients
p = 0.044
significant positive effects for ratings of intervention 'usefulness'
#2
brief mindfulness-based intervention (MBI)
increase
pain self-efficacy
persistent pain patients
p = 0.039
significant positive effects for pain self-efficacy
#3
Abstract

A pilot-randomised controlled trial (RCT) examined the effects of a brief mindfulness-based intervention (MBI) on persistent pain patients and assessed the feasibility of conducting a definitive RCT. A brief (15 min) mindfulness body-scan audio was compared with an active control administered in a clinic and then used independently over 1 month. Immediate effects of the intervention were assessed with brief measures of pain severity, distraction and distress. Assessments at baseline, 1 week and 1 month included pain severity and interference, mood, pain-catastrophizing, mindfulness, self-efficacy, quality of life and intervention acceptability. Of 220 referred patients, 147 were randomised and 71 completed all assessments. There were no significant immediate intervention effects. There were significant positive effects for ratings of intervention 'usefulness' at 1 week (p = 0.044), and pain self-efficacy at 1 month (p = 0.039) for the MBI group compared with control. Evidently, it is feasible to recruit persistent pain patients to a brief MBI study. Strategies are needed to maximise retention of participants.Trial registration Current controlled trials ISRCTN61538090. Registered 20 April 2015.

Medical Subject Headings (MeSH)
AdultAgedCatastrophizationChronic PainFemaleHumansMaleMiddle AgedMindfulnessPilot ProjectsQuality of LifeSelf EfficacyTreatment Outcome
Study Links
Quality Scores
SafetyNot Assessed
Efficacy65/10
Quality75/10
Citation Metrics
Total Citations7
Citations/Year1.2
Relative Citation Ratio0.56
NIH Percentile30.5%
Research Impact Scores
APT Score0.50
Weight Score2.02
Normalized Score0.61
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