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Problem Adaptation Therapy for Mild Cognitive Impairment and Depression (PATH-MCI)

Primary Purpose

Cognitive Impairment, Depression

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
PATH-MCI
Supportive Therapy
Sponsored by
Weill Medical College of Cornell University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Cognitive Impairment

Eligibility Criteria

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

Inclusion Criteria:

  • Amnestic MCI as defined by Albert et al
  • Montgomery Asberg Depression Rating Scale (MADRS) greater than 7 and MADRS total less than 30
  • Participants will be off antidepressants, cholinesterase inhibitors or memantine, or on a stable dosage for at least 12 weeks without any medical recommendation to adjust dosage in next 3 months (during treatment)
  • Clinical Dementia Rating (CDR) = 0.5 at screening
  • Subjects will have capacity to consent

Exclusion Criteria:

  • Deemed to have a significant suicide risk as assessed by site PI and clinical team
  • Deemed too unstable medically or neurologically to safely enroll in a research trial
  • Deemed too psychiatrically unstable to safely enroll in randomized trial of psychotherapy. Requiring psychiatric hospitalization at baseline for safety.
  • Current involvement in psychotherapy
  • Lack of English fluency

Sites / Locations

  • Johns Hopkins University School of MedicineRecruiting
  • Montefiore Medical Center
  • Weill Cornell MedicineRecruiting
  • Weill Cornell Institute of Geriatric Psychiatry, Weill Cornell MedicineRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

PATH-MCI

Supportive Therapy

Arm Description

Problem Adaptation Therapy for Mild Cognitively Impaired Adults (PATH-MCI) differs from standard of care psychotherapy by offering a combination of emotion regulation techniques with the provision of environmental adaptation tools (notes, checklists, calendars, etc.), the use of the WellPATH app, and the participation of a willing and available caregiver.

Supportive Therapy focuses on: 1. Facilitating expression of affect; 2. Conveying to the patient that he or she is understood; 3. Offering empathy; and 4. Highlighting positive experiences. The ST manual aims to standardize nonspecific therapeutic factors.

Outcomes

Primary Outcome Measures

Change in Global Cognition assessed by RBANS
Global cognition will be assessed by the Repeatable Battery for the Assessment of Neuropsychological Status Total Score (RBANS)

Secondary Outcome Measures

Change in disability function assessed with WHODAS-II
Disability function, as measured by the World Health Organization Disability Assessment Schedule-II (WHODAS-II) Total score
Change in Depression assessed by MADRS
Depression assessed by Montgomery Asberg Depression Rating Scale (MADRS) Total Score
Change in Episodic Memory assessed by subscale of RBANS
Delayed Recall subscale of Repeatable Battery for the Assessment of Neuropsychological Status (RBANS)
Change in Executive Function assessed by Trail Making Test
Trail Making Test

Full Information

First Posted
January 27, 2017
Last Updated
February 22, 2023
Sponsor
Weill Medical College of Cornell University
Collaborators
Johns Hopkins University, Montefiore Medical Center, National Institute on Aging (NIA)
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1. Study Identification

Unique Protocol Identification Number
NCT03043573
Brief Title
Problem Adaptation Therapy for Mild Cognitive Impairment and Depression
Acronym
PATH-MCI
Official Title
Problem Adaptation Therapy for Mild Cognitive Impairment and Depression
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
July 1, 2017 (Actual)
Primary Completion Date
March 31, 2023 (Anticipated)
Study Completion Date
March 31, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Weill Medical College of Cornell University
Collaborators
Johns Hopkins University, Montefiore Medical Center, National Institute on Aging (NIA)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The present collaborative R01 study, between Cornell and Johns Hopkins, aims to compare Problem Adaptation Therapy for Mild Cognitively Impaired Older Adults (PATH-MCI) vs. Supportive Therapy for Cognitively Impaired Older Adults (ST-CI) in improving cognitive, affective, and functioning outcomes.
Detailed Description
The present collaborative R01 study, between Cornell and Johns Hopkins, aims to compare Problem Adaptation Therapy for Mild Cognitively Impaired Older Adults (PATH-MCI) vs. Supportive Therapy for Cognitively Impaired Older Adults (ST-CI) in improving cognitive, affective and functioning outcomes. Psychotherapy, also known as talking therapy, is the use of psychological methods to help a person change and overcome problems in desired ways. PATH-MCI differs from standard of care psychotherapy by offering a combination of emotion regulation techniques with the provision of environmental adaptation tools (notes, checklists, calendars, etc.), the use of the WellPATH app, and the participation of a willing and available caregiver. Supportive Therapy incorporates standard of care approaches by using non-specific techniques to provide a supportive environment and help patients to express their feelings & focus on their strengths and abilities. The investigators plan to randomize 80 treatment subjects, older adults (40 at Cornell and 40 at Johns Hopkins) with MCI-depression. 80 study partners may also be potentially recruited. Both sites have shown feasibility of recruitment, randomization, retention, and assessment procedures for patients with MCI. Cornell has shown evidence of administration of PATH in this population. Certified mental health clinicians in PATH-MCI and ST-CI will administer 15 in-office sessions in six months. The investigators propose to compare the effects of 15 sessions (12 weekly in first 12 weeks and 3 monthly booster sessions afterwards) of PATH-MCI vs. ST-CI in 80 older adults (treatment subjects) with MCI-depression. Research assistants, unaware of study hypotheses and participant randomization status, will perform research assessments at baseline and at 6 (no cognitive measures), 12, 24, 36 (no cognitive measures) and 52 weeks after randomization. There will also be optional blood draws at study entry, 12, and 52 weeks. The purpose of the blood draws is to better understand whether response to psychotherapy treatment is affected by genes, by inflammation, or by the possible memory factor called BDNF (brain-derived neurotrophic factor). Also, all therapy sessions will be audiotaped (if the patient consents) and Dr. Shermer (a clinician outside of the Weill Cornell Institute of Geriatric Psychiatry) will evaluate randomly selected sessions and rate the therapists' adherence and competence based on the PATH-MCI and ST Adherence Scales The study partner will provide information about the treatment subject and participate in treatment if agreed by the treatment subject. To explore the effects of PATH-MCI on the study partner, the investigators will collect the following data from the study partner: demographic, burden (Short Zarit Burden interview), and treatment satisfaction (Client Satisfaction Questionnaire).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cognitive Impairment, Depression

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
PATH-MCI
Arm Type
Experimental
Arm Description
Problem Adaptation Therapy for Mild Cognitively Impaired Adults (PATH-MCI) differs from standard of care psychotherapy by offering a combination of emotion regulation techniques with the provision of environmental adaptation tools (notes, checklists, calendars, etc.), the use of the WellPATH app, and the participation of a willing and available caregiver.
Arm Title
Supportive Therapy
Arm Type
Active Comparator
Arm Description
Supportive Therapy focuses on: 1. Facilitating expression of affect; 2. Conveying to the patient that he or she is understood; 3. Offering empathy; and 4. Highlighting positive experiences. The ST manual aims to standardize nonspecific therapeutic factors.
Intervention Type
Behavioral
Intervention Name(s)
PATH-MCI
Intervention Description
Problem Adaptation Therapy for Mild Cognitively Impaired Adults (PATH-MCI) differs from standard of care psychotherapy by offering a combination of emotion regulation techniques with the provision of environmental adaptation tools (notes, checklists, calendars, etc.), the use of the WellPATH app, and the participation of a willing and available caregiver.
Intervention Type
Behavioral
Intervention Name(s)
Supportive Therapy
Other Intervention Name(s)
ST
Intervention Description
ST focuses on: 1. facilitating expression of affect; 2. conveying to the patient that he or she is understood; 3. offering empathy; and 4. highlighting positive experiences. The ST manual aims to standardize nonspecific therapeutic factors.
Primary Outcome Measure Information:
Title
Change in Global Cognition assessed by RBANS
Description
Global cognition will be assessed by the Repeatable Battery for the Assessment of Neuropsychological Status Total Score (RBANS)
Time Frame
Baseline, 12, 24, and 52 Weeks
Secondary Outcome Measure Information:
Title
Change in disability function assessed with WHODAS-II
Description
Disability function, as measured by the World Health Organization Disability Assessment Schedule-II (WHODAS-II) Total score
Time Frame
Baseline, 6, 12, 24, 36, and 52 Weeks
Title
Change in Depression assessed by MADRS
Description
Depression assessed by Montgomery Asberg Depression Rating Scale (MADRS) Total Score
Time Frame
Baseline, 6, 12, 24, 36, and 52 Weeks
Title
Change in Episodic Memory assessed by subscale of RBANS
Description
Delayed Recall subscale of Repeatable Battery for the Assessment of Neuropsychological Status (RBANS)
Time Frame
Baseline, 12, 24, and 52 Weeks
Title
Change in Executive Function assessed by Trail Making Test
Description
Trail Making Test
Time Frame
Baseline, 12, 24, and 52 Weeks
Other Pre-specified Outcome Measures:
Title
Change in Stress Reduction assessed by Perceived Stress Scale
Description
Perceived Stress Scale
Time Frame
Baseline, 6, 12, 24, 36, and 52 Weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
60 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Amnestic MCI as defined by Albert et al Montgomery Asberg Depression Rating Scale (MADRS) greater than 7 and MADRS total less than 30 Participants will be off antidepressants, cholinesterase inhibitors or memantine, or on a stable dosage for at least 12 weeks without any medical recommendation to adjust dosage in next 3 months (during treatment) Clinical Dementia Rating (CDR) = 0.5 at screening Subjects will have capacity to consent Exclusion Criteria: Deemed to have a significant suicide risk as assessed by site PI and clinical team Deemed too unstable medically or neurologically to safely enroll in a research trial Deemed too psychiatrically unstable to safely enroll in randomized trial of psychotherapy. Requiring psychiatric hospitalization at baseline for safety. Current involvement in psychotherapy Lack of English fluency
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Dimitris Kiosses, PhD
Phone
9149974381
Email
dkiosses@med.cornell.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Laurie Evans, MS
Phone
9146829100
Ext
1012570
Email
lad9011@med.cornell.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dimitris Kiosses, PhD
Organizational Affiliation
Weill Medical College of Cornell University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Johns Hopkins University School of Medicine
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21224
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Paul B Rosenberg, MD
Phone
410-550-9883
Email
prosenb9@jhmi.edu
First Name & Middle Initial & Last Name & Degree
Samantha Horn
Phone
410-550-9022
Email
shorn8@jhmi.edu
Facility Name
Montefiore Medical Center
City
Bronx
State/Province
New York
ZIP/Postal Code
10461
Country
United States
Individual Site Status
Completed
Facility Name
Weill Cornell Medicine
City
New York
State/Province
New York
ZIP/Postal Code
10065
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dimitris Kiosses, PhD
Phone
914-997-4381
Email
dkiosses@med.cornell.edu
First Name & Middle Initial & Last Name & Degree
Laurie Evans, MS
Phone
914-682-9100
Ext
1012570
Email
lad9011@med.cornell.edu
Facility Name
Weill Cornell Institute of Geriatric Psychiatry, Weill Cornell Medicine
City
White Plains
State/Province
New York
ZIP/Postal Code
10605
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dimitris Kiosses, PhD
Phone
914-997-4381
Email
dkiosses@med.cornell.edu
First Name & Middle Initial & Last Name & Degree
Laurie Evans, MS
Phone
914-682-9100
Ext
1012570
Email
lad9011@med.cornell.edu

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Data will be available as per NIH's data sharing policy.
IPD Sharing Time Frame
Data will be available as per NIH's data sharing policy.
IPD Sharing Access Criteria
Access criteria is determined by NIH and can be requested by applying online.
IPD Sharing URL
https://nda.nih.gov/

Learn more about this trial

Problem Adaptation Therapy for Mild Cognitive Impairment and Depression

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