Ignite Creation Date:
2024-05-05 @ 11:54 AM
Last Modification Date:
2024-10-26 @ 9:16 AM
Study NCT ID:
NCT00169286
Status:
COMPLETED
Last Update Posted:
2017-10-13
First Post:
2005-09-12
Brief Title:
Organized Self-management Support for Chronic Depression
Sponsor:
Kaiser Permanente
Organization:
Kaiser Permanente
Study Overview
Official Title:
Organized Self-management Support for Chronic Depression
Status:
COMPLETED
Status Verified Date:
2017-10
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This study aims to adapt and pilot test two core elements of an organized care program systematic telephone outreach and monitoring to improve quality and continuity of pharmacotherapy and structured psychoeducational group programs focused on patient activation and self-management in a population-based sample of patients with chronic or recurrent depression
Detailed Description:
This study aims to adapt and pilot test two core elements of an organized care program systematic telephone outreach and monitoring to improve quality and continuity of pharmacotherapy and structured psychoeducational group programs focused on patient activation and self-management in a population-based sample of patients with chronic or recurrent depression Two forms of group self-management training will be evaluated a Peer-Led Chronic Disease Self-Management Group after that developed by Lorig and colleagues and a Therapist-Led Cognitive-Behavioral Therapy Group Approximately 100 patients with chronic or recurrent depression were randomly assigned to one of four conditions 1 usual care 2 phone care management 3 phone care management plus peer-led self-management group or 4 phone care management plus therapist-led CBT group Blinded assessments will examine clinical outcomes SCL depression score depression diagnosis by SCID functional outcomes and process variables self-efficacy for managing depression use of coping strategies over 12 months If patients choose not to participate in treatment reasons for dropout were assessed The data collected will provide1 an evaluation of the feasibility and acceptability including recruitment intervention uptake and continued participation of the intervention programs 2 preliminary evaluation of effectiveness ie the effects of each intervention on patient outcomes and process of care and 3 information to inform the design and implementation of a full-scale effectiveness trial refinement of intervention programs and measurement strategy necessary sample size
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None