Skip to main content
Clinical Trials/NCT01706731
NCT01706731
Unknown
N/A

A Randomized Controlled Trial of Cognitive Behavior Therapy Provided by Buddhist Monks vs. Treatment as Usual in the Treatment of Late Life-depression

Chiang Mai University1 site in 1 country62 target enrollmentOctober 2012

Overview

Phase
N/A
Intervention
Not specified
Conditions
Major Depressive Disorder
Sponsor
Chiang Mai University
Enrollment
62
Locations
1
Primary Endpoint
Evidence of clinically depression confirmed by clinician
Last Updated
13 years ago

Overview

Brief Summary

This research is to study the effectiveness of cognitive behavioral therapy-CBT and Psychotherapy by trained buddhist monks. There are generally accepted that both cognitive and Buddhist concepts are related. This randomized controlled trial is to study the elderly participants who suffer major depressive disorder according to DSM-IV. The subjects will be divided into two groups. The experimental group will receive 12 sessions of CBT 2 times per week for 6 weeks in addition to usual treatment. The control group will receive treatment as usual and general conversation (non-CBT) with monks. Pretreatment factors (such as attachment style, interpersonal factors) of both therapist monks and patient participants will be studied.

Registry
clinicaltrials.gov
Start Date
October 2012
End Date
October 2013
Last Updated
13 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Nahathai Wongpakaran

Associate Professor

Chiang Mai University

Eligibility Criteria

Inclusion Criteria

  • Meet criteria for Major depressive disorder
  • receiving antidepressant

Exclusion Criteria

  • presence of intense suicidal intent behaviors that require inpatient admission
  • history of alcohol or drug dependence
  • presence of hallucinations or delusions
  • currently receiving electroconvulsive therapy or repetitive-transcranial magnetic stimulation,
  • patients' involvement in other clinical trials.

Outcomes

Primary Outcomes

Evidence of clinically depression confirmed by clinician

Time Frame: 2 months after the end of the intervention

Depression will be assessed by HAMD-7 (McIntyre, 2005)

Depression- self report

Time Frame: 2 month after the end of the inetrvention

depression will be assessed by Geriatric Depression Scale (GDS)(Shiekh \& Yesavage, 1986)

Secondary Outcomes

  • Dimensional psychological distress (anxiety, depression,and somatization)(week 6, 12, 20)
  • Dimensional psychological distress ( perception of stress)(Week 6, 12, 20)

Study Sites (1)

Loading locations...

Similar Trials