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Telephone-Based Counseling for Depression in Parkinson's Disease (TH-CBT)

Primary Purpose

Depression, Parkinson's Disease

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
TH-CBT
Enhanced Usual Care
Sponsored by
Rutgers, The State University of New Jersey
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Depression

Eligibility Criteria

35 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Confirmed diagnosis of Parkinson's disease.
  2. Clinically significant depressive symptoms (e.g., symptoms are pervasive, distressing, and make life harder). The presence of a formal depressive disorder will be determined by study staff based on standardized criteria (e.g., SCID).
  3. 35-85 years old
  4. Stable medication regimen ≥ 6 weeks
  5. No change in mental health treatment in the past 2 months
  6. Family member or friend willing to participate
  7. Access to a telephone
  8. Live in the United States of America (USA)

Exclusion Criteria:

  1. Suicidal plans or intent
  2. Probable Dementia or Significant Cognitive Impairment
  3. Significant motor fluctuations (i.e., ≥ 50% of the day)
  4. Unstable medical conditions
  5. Bipolar, Psychotic Spectrum, or Substance Abuse Disorders

Sites / Locations

  • Rutgers University-Robert Wood Johnson Medical School

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

TH-CBT

Enhanced Usual Care

Arm Description

The treatment works by teaching people with PD (PWP) the coping skills needed to manage their emotional reactions to the numerous challenges posed by the disease. Specifically, the treatment targets maladaptive thought patterns (e.g., I have no control; I am helpless) and behaviors (e.g., social isolation, lack of exercise, poor sleep habits, excessive worry), and critically, provides caregivers with the tools needed to encourage the PWPs' practice of their newly acquired coping skills. Treatment is administered over the phone and no travel is required.

All participants will continue to receive their routine medical treatment under the supervision of their personal doctors (e.g., neurologists, psychiatrists, primary care physicians, therapists) while participating in the study. This routine treatment (e.g., usual care) will be further enhanced with the provision of written educational materials for effective coping with PD, the close clinical monitoring of depressive symptoms by study staff, and the provision of counseling resources in the local community.

Outcomes

Primary Outcome Measures

Depression on the Hamilton Depression Rating Scale
clinician-administered scale- depression

Secondary Outcome Measures

Treatment Response on the Clinical Global Impression- Improvement Scale
clinician-administered scale- treatment response
Anxiety on the Hamilton Anxiety Rating Scale
clinician administered scale-anxiety
Quality of life on the SF-36
self-report scale- quality of life

Full Information

First Posted
July 21, 2015
Last Updated
February 15, 2019
Sponsor
Rutgers, The State University of New Jersey
Collaborators
Michael J. Fox Foundation for Parkinson's Research
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1. Study Identification

Unique Protocol Identification Number
NCT02505737
Brief Title
Telephone-Based Counseling for Depression in Parkinson's Disease
Acronym
TH-CBT
Official Title
Improving Access to Depression Care in Parkinson's Disease: A Telehealth Approach
Study Type
Interventional

2. Study Status

Record Verification Date
February 2019
Overall Recruitment Status
Completed
Study Start Date
July 2015 (Actual)
Primary Completion Date
June 30, 2018 (Actual)
Study Completion Date
June 30, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rutgers, The State University of New Jersey
Collaborators
Michael J. Fox Foundation for Parkinson's Research

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
There is a critical need for treatments that address depression and barriers to mental health care in Parkinson's disease (PD). This randomized-controlled trial will evaluate a 10-session telephone-guided cognitive behavioral self-help program (TH-CBT) for depression in PD (dPD). 72 people with dPD (and their caregivers) will receive either TH-CBT plus enhanced usual care (INTERVENTION GROUP) or enhanced usual care only (CONTROL GROUP). Groups will be compared at baseline, midpoint, endpoint, and 1 and 6 months post-treatment. Participants assigned to the control group with have the opportunity to receive the experimental intervention (TH-CBT) after the data collection period (e.g., after the 6-month follow-up evaluation). Given the public health impact of improved depression treatment in PD, the knowledge to be gained may be significant and the project could directly impact clinical practice.
Detailed Description
All study procedures, including the initial evaluation, study treatment sessions, and follow-up study assessments, take place over the phone and no travel is required. All PWP across the USA may participate. All participants will continue to receive their routine medical treatment under the supervision of their personal doctors (e.g., neurologists, psychiatrists, primary care physicians, therapists) while participating in the study. In addition to usual care, half of the participants in the study will receive the experimental telehealth treatment (TH-CBT; intervention group), immediately after enrolling in the research program. The other half will only receive usual care (control group) and will have the option to receive TH-CBT, after completing all study related assessments (9 months after the initial evaluation). Group assignment will be decided randomly (i.e., by chance). Study eligibility will be determined by a qualified professional. Those who qualify for participation will be randomly assigned (e.g., flip of a coin) to either the intervention (TH-CBT) or the control group (enhanced usual care). Participants assigned to the TH-CBT group will receive a 10-chapter CBT self-help treatment workbook, tailored to the unique needs of people with PD, immediately following enrollment. Participants will read and complete one treatment module per week (approximately 60 minutes per module plus practice exercises throughout the week). The treatment materials will review different coping skills for the effective management of depression. Study therapists will call participants to review the treatment material over the phone every week (after every chapter) or every other week (after ever 2 chapters), based on participant needs. These telephone-based counseling sessions will last 60 minutes. It will take approximately 10 weeks to complete the study treatment materials. A family member or friend (carepartner) will also be asked to participate in 3-4 separate educational sessions (30-60 minutes each), evenly dispersed throughout the 10 week TH-CBT treatment period. The study treatment provided to the care-partner will teach the care-partner how to best support the participant with PD as he/she tries to incorporate the information learned during the study treatment, in day-to-day life. Participants will be re-evaluated 6, 11, 15, and 35 weeks after the initial evaluation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression, Parkinson's Disease

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
72 (Actual)

8. Arms, Groups, and Interventions

Arm Title
TH-CBT
Arm Type
Experimental
Arm Description
The treatment works by teaching people with PD (PWP) the coping skills needed to manage their emotional reactions to the numerous challenges posed by the disease. Specifically, the treatment targets maladaptive thought patterns (e.g., I have no control; I am helpless) and behaviors (e.g., social isolation, lack of exercise, poor sleep habits, excessive worry), and critically, provides caregivers with the tools needed to encourage the PWPs' practice of their newly acquired coping skills. Treatment is administered over the phone and no travel is required.
Arm Title
Enhanced Usual Care
Arm Type
Other
Arm Description
All participants will continue to receive their routine medical treatment under the supervision of their personal doctors (e.g., neurologists, psychiatrists, primary care physicians, therapists) while participating in the study. This routine treatment (e.g., usual care) will be further enhanced with the provision of written educational materials for effective coping with PD, the close clinical monitoring of depressive symptoms by study staff, and the provision of counseling resources in the local community.
Intervention Type
Behavioral
Intervention Name(s)
TH-CBT
Intervention Description
Telephone-Based Cognitive Behavioral Therapy (TH-CBT). A 10-session treatment protocol that incorporates behavioral activation, thought monitoring and restructuring, relaxation training, worry control, sleep hygiene, and caregiver psychoeducation and support
Intervention Type
Other
Intervention Name(s)
Enhanced Usual Care
Intervention Description
Community-based treatment as usual and supplemental reading material
Primary Outcome Measure Information:
Title
Depression on the Hamilton Depression Rating Scale
Description
clinician-administered scale- depression
Time Frame
9 months
Secondary Outcome Measure Information:
Title
Treatment Response on the Clinical Global Impression- Improvement Scale
Description
clinician-administered scale- treatment response
Time Frame
9- months
Title
Anxiety on the Hamilton Anxiety Rating Scale
Description
clinician administered scale-anxiety
Time Frame
9-months
Title
Quality of life on the SF-36
Description
self-report scale- quality of life
Time Frame
9-months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
35 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Confirmed diagnosis of Parkinson's disease. Clinically significant depressive symptoms (e.g., symptoms are pervasive, distressing, and make life harder). The presence of a formal depressive disorder will be determined by study staff based on standardized criteria (e.g., SCID). 35-85 years old Stable medication regimen ≥ 6 weeks No change in mental health treatment in the past 2 months Family member or friend willing to participate Access to a telephone Live in the United States of America (USA) Exclusion Criteria: Suicidal plans or intent Probable Dementia or Significant Cognitive Impairment Significant motor fluctuations (i.e., ≥ 50% of the day) Unstable medical conditions Bipolar, Psychotic Spectrum, or Substance Abuse Disorders
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Roseanne D Dobkin, PhD
Organizational Affiliation
Rutgers Robert Wood Johnson Medical School
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rutgers University-Robert Wood Johnson Medical School
City
Piscataway
State/Province
New Jersey
ZIP/Postal Code
08854
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
32238507
Citation
Dobkin RD, Mann SL, Gara MA, Interian A, Rodriguez KM, Menza M. Telephone-based cognitive behavioral therapy for depression in Parkinson disease: A randomized controlled trial. Neurology. 2020 Apr 21;94(16):e1764-e1773. doi: 10.1212/WNL.0000000000009292. Epub 2020 Apr 1.
Results Reference
derived

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Telephone-Based Counseling for Depression in Parkinson's Disease

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