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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01323699
Other study ID # H-28002
Secondary ID
Status Completed
Phase Phase 1/Phase 2
First received March 25, 2011
Last updated April 30, 2013
Start date November 2011
Est. completion date February 2013

Study information

Verified date April 2013
Source Michael Debakey Veterans Affairs Medical Center
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review BoardUnited States: Federal Government
Study type Interventional

Clinical Trial Summary

Behavioral Treatments for Anxiety and Depression (BehTA-D) is a research study for anxiety and depression in individuals with Parkinson's disease (PD). The research clinicians try to teach skills that may help participants cope with anxiety and depression in the context of Parkinson's disease. Research clinicians will also discuss ways improve management of Parkinson's symptoms. Other skills taught include how to relax, change thinking, add in meaningful pleasant activity.


Description:

Components of evidence-based cognitive behavioral therapy (CBT) treatments from current manuals developed for depression and anxiety will be used to construct the 8-week treatment program. The flexibility of modular based treatment allows patients and counselors to personalize interventions and skills for managing anxiety and depressive symptoms. The first treatment session will be in-person. All following sessions will be provided by telephone. Caregivers will have the option of being involved in 2 ways throughout treatment - as a "coach" to facilitate use of new skills by their loved one with PD and as a recipient of stress- management support. The scope of caregiver involvement will vary across patients, based on their preference. Involved caregivers will be given the opportunity to participate in 1 telephone-based stress-management session and 1 follow-up call scheduled individually during the first 4 weeks of treatment.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date February 2013
Est. primary completion date February 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

1. Have a confirmed diagnosis of idiopathic Parkinson's disease

2. Have significant anxiety and/or depressive symptoms as indicated by a score of greater than 4 on the Geriatric Depression Scale -15 or greater than 5 on the Hospital Anxiety and Depression anxiety subscale

Exclusion Criteria:

Patients will be excluded if they have cognitive impairment as indicated by the Montreal Cognitive Assessment (MoCA < 23) or if they have a condition that threatens their safety or life including suicidal intent, current psychosis, bipolar, substance abuse or impulse control disorders within the past month.

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Intervention

Behavioral:
Cognitive Behavioral Therapy
A modified version of existing Cognitive Behavioral Treatment and Self-management manuals.

Locations

Country Name City State
United States Michael E. DeBakey Veteran Affairs Medical Center Houston Texas

Sponsors (2)

Lead Sponsor Collaborator
Michael Debakey Veterans Affairs Medical Center South Central VA Mental Illness Research, Education & Clinical Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Hospital Anxiety and Depression Scale and Hamilton Anxiety Scale Baseline, 3-months and 4-months No
Primary Hamilton Depression Scale and Geriatric Depression Scale - 15 Baseline, 3-months, and 4-months No
Secondary Parkinson's Disease Questionnaire -8 Baseline, 3-months and 4-months No
Secondary Client Satisfaction Questionnaire 3-months and 4-months No
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