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MBCT vs HEP in Patients With Late-Life Depression

Primary Purpose

Depression in Old Age, Cognitive Decline

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Mindfulness-Based Cognitive Therapy
Health Enhancement Program
Sponsored by
Lady Davis Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Depression in Old Age focused on measuring Late-life depression, Cognitive Decline, Mindfulness-Based Cognitive Therapy, Behavioural Activation, Executive Functioning, Processing Speed

Eligibility Criteria

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

Inclusion Criteria:

  • Major depressive disorder as assessed by the Mini International Neuropsychiatric Inventory (MINI). Following the MINI assessment, a psychiatrist will verify the diagnosis of major depressive disorder.
  • Hamilton Depression scale (HAM-D17) score ≥ 10
  • Participants willing and able to attend ≥75% of MBCT/HEP sessions
  • Sufficient hearing to follow verbal instructions
  • Adequate understanding of English and/or French
  • Ability to sit for 40 minutes without discomfort.

Exclusion Criteria:

  • Inability to provide informed consent
  • Evidence of dementia as defined by MoCA scores
  • Lifetime diagnosis of bipolar I or II disorder, primary psychotic disorder (e.g. schizophrenia, schizoaffective disorder), and/or severe personality disorder interfering with ability to function in a group
  • Substance abuse/dependence within the past 6 months
  • High suicide risk (e.g., active suicidal ideation and/or current/recent intent or plan)
  • Non-correctable, clinically significant sensory impairment
  • Significant impairments in fine motor skills
  • Acutely unstable medical illnesses, including delirium, acute cerebrovascular/cardiovascular events within the last 6 months; having a terminal medical diagnosis with prognosis of less than 12 months;
  • Currently practicing any mind-body intervention on a regular basis
  • Unwilling or unable to remain on the same psychotropic medications (includes dosage) for the first 8 weeks of the study
  • Any of the following contraindications for a magnetic resonance study: pacemaker, aneurysm clip, heart/vascular clip, prosthetic valve, metal prosthesis, claustrophobia, metal fragments in body, and transdermal patches.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    Mindfulness-Based Cognitive Therapy

    Health Enhancement Program

    Arm Description

    Group sessions 2 hours/week, for 8 weeks, based on the manualized protocol developed by co-I Dr. Segal and will be delivered by social workers (or equivalent) with ≥3 years of experience delivering MBCT and training for official certification from the Center for Mindfulness Studies (Toronto).

    Group sessions 2 hrs/week for 8 weeks, and amount of home practice (~30 mins/day, 6 days/week). HEP will be delivered by social workers (or equivalent) who have received the official training course from HEP's developers at the University of Wisconsin.

    Outcomes

    Primary Outcome Measures

    Hamilton Depression Rating Scale (HAM-D17) score
    Depression Symptoms, rated from 0 tp 54. Higher scores mean more depressive symptoms.

    Secondary Outcome Measures

    Hippocampal volume
    T1 weighted MPRAGE will be acquired (TE/TR=2.98 ms/2300 ms, TI=900 ms, α=9°, FOV= 256 x 240 x 192 mm, GRAPPA of 2, 5 min). Volumetry of the hippocampus and its subfields will be identified using the MAGeT Brain algorithm.
    Resting-state functional connectivity
    Resting-state functional MRI data will be acquired using simultaneous multislice echo planar imaging sequence (62) with a scan time of ~5 mins, with the following parameters: TE/TR=30 ms/1000 ms, 300 frames, slice thickness= 2.5 mm, and 2.5 mm isotropic in-plane resolution, and slice acceleration factor (SMS) of 4. A matching B0 field map will be acquired with an approximate scan time of 1.5 min, with the following parameters: TE 1=4.92 ms, TE 2=7.38 ms, TR=688 ms.
    WAIS-IV Digit Symbol score
    Processing Speed. Scores range from 0 to 100 with higher scores indicating higher processing speed.
    WAIS- IV Digit Span score
    Executive Functioning. Scores range from 0 to 16 with higher scores indicating better executive functioning.

    Full Information

    First Posted
    April 26, 2022
    Last Updated
    May 4, 2022
    Sponsor
    Lady Davis Institute
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05366088
    Brief Title
    MBCT vs HEP in Patients With Late-Life Depression
    Official Title
    Mindfulness-Based Cognitive Therapy (MBCT) vs. Health Enhancement Program (HEP) Active Control for the Treatment of Late-Life Depression: An RCT
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    May 2022
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    December 1, 2022 (Anticipated)
    Primary Completion Date
    December 1, 2025 (Anticipated)
    Study Completion Date
    December 1, 2025 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Lady Davis Institute

    4. Oversight

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

    5. Study Description

    Brief Summary
    Study Design & Recruitment: Phase III randomized controlled trial (RCT) with 200 patients. Participants with a diagnosis of late-life depression (LLD), excluding dementia and other psychiatric comorbidities, will be recruited at three health networks. LLD patients had no earlier depressive episodes before the age of 65. Interventions: Mindfulness-based Cognitive Therapy (MBCT) or Health Enhancement Program (HEP) for 8-weeks, in addition to TAU. MBCT and HEP will have the same group sizes, meeting frequency, and amount of home practice. HEP is a recognized active control where participants learn about diet and exercise, but not meditation.
    Detailed Description
    Late life depression (LLD) affects 5 million American seniors yearly with $1.81 billion in direct health-care costs. Biomarkers of LLD have consistently been linked to elevated dementia risk. Mindfulness-based cognitive therapy (MBCT) holds promise for treating symptoms of depression, ameliorating cognitive deficits and preventing decline in older adults by targeting brain circuits implicated in memory and attention. While preliminary findings are promising, the effects of mindfulness on cognition and brain markers have not been assessed in older adults with depression who are especially vulnerable to cognitive decline. This proposed research will explore 1) whether MBCT's mechanism of action in treating symptoms of depression and preventing cognitive decline is behavioural activation or mindfulness, two components of MBCT, 2) the role of environmental factors, 3) whether benefits persist in the medium term, and 4) the persistence of key cognitive and brain markers associated with the treatment of LLD. Two-hundred and thirteen (n = 213) patients with LLD will be recruited at various centres in Montreal (affiliated with McGill University, Université de Montréal and University of Toronto). Participants will undergo stratified randomization to either MBCT or Health Enhancement Program (HEP) intervention groups. The investigators will assess changes in (1) depression severity, (2) processing speed and executive functioning, (3) hippocampal volume, resting-state functional connectivity and vascular risk factors, and (4) other exploratory physiological and mood-based measures, at baseline (0 weeks), post intervention (8 weeks), and 26 weeks after baseline. Raters and clinicians will be blinded to group allocation while participants will be blinded to the study hypotheses. The proposed study will assess the clinical potential of MBCT to improve symptoms of depression, as well as examine its impact on cognitive impairments and neurobiological markers, and thus inform its use as a promising adjunct in the treatment of LLD. If MBCT is found to be effective in treating LLD and preventing cognitive decline, the potential exists to implement this intervention at the study sites, across Canada, and internationally.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Depression in Old Age, Cognitive Decline
    Keywords
    Late-life depression, Cognitive Decline, Mindfulness-Based Cognitive Therapy, Behavioural Activation, Executive Functioning, Processing Speed

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    213 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Mindfulness-Based Cognitive Therapy
    Arm Type
    Experimental
    Arm Description
    Group sessions 2 hours/week, for 8 weeks, based on the manualized protocol developed by co-I Dr. Segal and will be delivered by social workers (or equivalent) with ≥3 years of experience delivering MBCT and training for official certification from the Center for Mindfulness Studies (Toronto).
    Arm Title
    Health Enhancement Program
    Arm Type
    Active Comparator
    Arm Description
    Group sessions 2 hrs/week for 8 weeks, and amount of home practice (~30 mins/day, 6 days/week). HEP will be delivered by social workers (or equivalent) who have received the official training course from HEP's developers at the University of Wisconsin.
    Intervention Type
    Behavioral
    Intervention Name(s)
    Mindfulness-Based Cognitive Therapy
    Intervention Description
    MBCT is an 8-week therapy integrating formal mindfulness meditation (e.g. breath and body awareness) and informal mindfulness (e.g. eating, walking). Participants are taught to attend non-judgmentally to present moment experiences. MBCT includes cognitive therapy techniques to target the ruminative thought processes and identification with negative emotions seen in depression. MBCT teaches participants how to disengage from habitual ("automatic") dysfunctional cognitive routines, in particular depression-related ruminative thought patterns that perpetuate depressive symptoms and increase vulnerability to relapse.
    Intervention Type
    Behavioral
    Intervention Name(s)
    Health Enhancement Program
    Intervention Description
    HEP teaches health-enhancing techniques and was designed by University of Wisconsin and NIH as a manualized active control group program for mindfulness-based intervention trials (53,54). We have tailored HEP to be structurally equivalent to MBCT. HEP will be delivered by social workers (or equivalent) who have received the official training course from HEP's developers at the University of Wisconsin. Participants will learn about health promotion, healthy diet, music, and gentle exercise, but not about breathing techniques or meditation.
    Primary Outcome Measure Information:
    Title
    Hamilton Depression Rating Scale (HAM-D17) score
    Description
    Depression Symptoms, rated from 0 tp 54. Higher scores mean more depressive symptoms.
    Time Frame
    26 weeks
    Secondary Outcome Measure Information:
    Title
    Hippocampal volume
    Description
    T1 weighted MPRAGE will be acquired (TE/TR=2.98 ms/2300 ms, TI=900 ms, α=9°, FOV= 256 x 240 x 192 mm, GRAPPA of 2, 5 min). Volumetry of the hippocampus and its subfields will be identified using the MAGeT Brain algorithm.
    Time Frame
    26 weeks
    Title
    Resting-state functional connectivity
    Description
    Resting-state functional MRI data will be acquired using simultaneous multislice echo planar imaging sequence (62) with a scan time of ~5 mins, with the following parameters: TE/TR=30 ms/1000 ms, 300 frames, slice thickness= 2.5 mm, and 2.5 mm isotropic in-plane resolution, and slice acceleration factor (SMS) of 4. A matching B0 field map will be acquired with an approximate scan time of 1.5 min, with the following parameters: TE 1=4.92 ms, TE 2=7.38 ms, TR=688 ms.
    Time Frame
    26 weeks
    Title
    WAIS-IV Digit Symbol score
    Description
    Processing Speed. Scores range from 0 to 100 with higher scores indicating higher processing speed.
    Time Frame
    26 weeks
    Title
    WAIS- IV Digit Span score
    Description
    Executive Functioning. Scores range from 0 to 16 with higher scores indicating better executive functioning.
    Time Frame
    26 weeks
    Other Pre-specified Outcome Measures:
    Title
    Vascular risk factors
    Description
    Fluid Attenuated Inversion Recovery (FLAIR) imaging sequence to detect small vessel disease burden and a Quantitative Susceptibility Mapping (QSM) assessment based on T2*-weighted imaging to assess microbleeds and iron accumulation which may lead to neurodegeneration.
    Time Frame
    26 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: Major depressive disorder as assessed by the Mini International Neuropsychiatric Inventory (MINI). Following the MINI assessment, a psychiatrist will verify the diagnosis of major depressive disorder. Hamilton Depression scale (HAM-D17) score ≥ 10 Participants willing and able to attend ≥75% of MBCT/HEP sessions Sufficient hearing to follow verbal instructions Adequate understanding of English and/or French Ability to sit for 40 minutes without discomfort. Exclusion Criteria: Inability to provide informed consent Evidence of dementia as defined by MoCA scores Lifetime diagnosis of bipolar I or II disorder, primary psychotic disorder (e.g. schizophrenia, schizoaffective disorder), and/or severe personality disorder interfering with ability to function in a group Substance abuse/dependence within the past 6 months High suicide risk (e.g., active suicidal ideation and/or current/recent intent or plan) Non-correctable, clinically significant sensory impairment Significant impairments in fine motor skills Acutely unstable medical illnesses, including delirium, acute cerebrovascular/cardiovascular events within the last 6 months; having a terminal medical diagnosis with prognosis of less than 12 months; Currently practicing any mind-body intervention on a regular basis Unwilling or unable to remain on the same psychotropic medications (includes dosage) for the first 8 weeks of the study Any of the following contraindications for a magnetic resonance study: pacemaker, aneurysm clip, heart/vascular clip, prosthetic valve, metal prosthesis, claustrophobia, metal fragments in body, and transdermal patches.

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    36118690
    Citation
    Bein M, Lesage M, Dikaios E, Chakravarty M, Segal Z, Royal I, Speechley M, Schiavetto A, Blumberger D, Sacchet MD, Therriault J, Gruber J, Tourjman V, Richard-Devantoy S, Nair V, Bruneau MA, Rej S, Lifshitz M, Sekhon H. Mindfulness-based cognitive therapy vs. a health enhancement program for the treatment of late-life depression: Study protocol for a multi-site randomized controlled trial. Front Aging Neurosci. 2022 Sep 1;14:976636. doi: 10.3389/fnagi.2022.976636. eCollection 2022.
    Results Reference
    derived

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    MBCT vs HEP in Patients With Late-Life Depression

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