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Clinical Trials/ISRCTN27934462
ISRCTN27934462
Completed
未知

The use of mindfulness-based cognitive therapy for improving quality of life for inflammatory bowel disease patients: a pilot randomised controlled trial with embedded process evaluation

niversity of Stirling (UK)0 sites40 target enrollmentAugust 9, 2013
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ConditionsInflammatory bowel diseaseDigestive SystemNoninfective enteritis and colitis

Overview

Phase
未知
Intervention
Not specified
Conditions
Inflammatory bowel disease
Sponsor
niversity of Stirling (UK)
Enrollment
40
Status
Completed
Last Updated
9 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
August 9, 2013
End Date
TBD
Last Updated
9 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
niversity of Stirling (UK)

Eligibility Criteria

Inclusion Criteria

  • •1\. Be able to verbally communicate and write in English (English language does not have to be first language)
  • •2\. Able to give informed consent
  • •3\. Age of 18 or over (no upper limit)
  • •4\. Confirmed diagnosis of Crohn's disease or Ulcerative Colitis (by clinician)
  • •5\. Ability to do light exercise (for example to lift arms above the head or bend knees)
  • •6\. To be able to commit to at least 6 sessions out of 8
  • •7\. To be able to commit to do home practice of up to 45 minutes daily over the 8 weeks of the study
  • •8\. No change of antidepressants (dose or type) within the last three months

Exclusion Criteria

  • •1\. Unable to give informed consent
  • •2\. Major psychiatric illness
  • •3\. Active alcohol or drug dependency
  • •4\. Scheduled for major surgery in the next three months
  • •5\. Participation in pharmacological study or psychological intervention study within the last six months or intention to participate in pharmacological study during the duration of this study
  • •6\. Have recently (within the last three months) been prescribed antidepressants
  • •7\. With exacerbated symptoms

Outcomes

Primary Outcomes

Not specified

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