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Clinical Trials/NCT01776645
NCT01776645
Completed
Not Applicable

Compassion Training and Pain

Stanford University1 site in 1 country56 target enrollmentJanuary 2013
ConditionsChronic Pain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chronic Pain
Sponsor
Stanford University
Enrollment
56
Locations
1
Primary Endpoint
Change in Brief Pain Inventory
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

The purpose of this study is to determine whether compassion training will improve the physical and psychological well-being of patients with chronic pain. The investigators also want to determine whether any benefit of compassion training in the patients "spreads" to significant others with whom the patient has a close relationship.

Registry
clinicaltrials.gov
Start Date
January 2013
End Date
May 2013
Last Updated
12 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age 18+ and chronic pain for \>6months
  • Pain over the last month
  • Ability to read, write, and converse in English
  • If being treated for pain condition, then stable treatment regimen.
  • For significant others:
  • 18 years of age or older 2)Ability to read, write, and converse in English

Exclusion Criteria

  • For patients and significant others:
  • Current or history of a psychological disorder that would interfere with study procedures, at the discretion of the researcher.
  • For patients only:
  • prior compassion meditation experience
  • on going legal action or disability claim
  • currently pregnant or planning to become pregnant

Outcomes

Primary Outcomes

Change in Brief Pain Inventory

Time Frame: Baseline and end of 9-week treatment protocol

Intensity - pain severity as measured by a 0 to 10 visual analogue scale. 0 = no pain, 10 = worst pain imaginable

Change in Chronic Pain Acceptance Questionnaire

Time Frame: Baseline and end of 9-week treatment protocol

Secondary Outcomes

  • Change in Brief Pain Inventory(Baseline to end of 9-week treatment protocol)

Study Sites (1)

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