Cognitive Behavioral Therapy, Self-Efficacy, and Depression in Persons With Chronic Pain
1 other identifier
observational
138
0 countries
N/A
Brief Summary
The investigators are exploring the role of Cognitive Behavioral Therapy (CBT), a treatment for depression, on self-efficacy (feeling empowered to accomplish a given task) and depression in persons with chronic pain and depression. Past research has shown that persons with chronic pain show improvement in self-efficacy and depression scores when they are using CBT. The Pain rehabilitation Center (PRC) at Mayo Clinic is adding CBT focused groups to better understand the role of CBT on self-efficacy and depression in persons with chronic pain and depression.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Oct 2009
Shorter than P25 for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 1, 2009
CompletedFirst Submitted
Initial submission to the registry
January 21, 2010
CompletedFirst Posted
Study publicly available on registry
January 25, 2010
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2010
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2010
CompletedMay 3, 2012
May 1, 2012
8 months
January 21, 2010
May 1, 2012
Conditions
Outcome Measures
Primary Outcomes (1)
Change on a depression and self-efficacy scale
3 weeks
Interventions
6 cognitive behavior therapy groups
Eligibility Criteria
Persons with chronic pain and depressive symptoms in a pain rehabilitation program.
You may qualify if:
- and over with chronic pain and
- score of 27 or higher on CES-D scale
You may not qualify if:
- or younger, no chronic pain,
- cognitively unable to participate in programming
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Mayo Cliniclead
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Virginia R Nash, RN, MS, CNS
Mayo Clinic
Study Design
- Study Type
- observational
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- RN, Clinical Nurse Specialist
Study Record Dates
First Submitted
January 21, 2010
First Posted
January 25, 2010
Study Start
October 1, 2009
Primary Completion
June 1, 2010
Study Completion
June 1, 2010
Last Updated
May 3, 2012
Record last verified: 2012-05