Supporting Our Caregivers In ADRD Learning (SOCIAL) (SOCIAL)

March 22, 2024 updated by: Christine S. Ritchie, MD, MPH, Massachusetts General Hospital

Supporting Our Caregivers In ADRD Learning (SOCIAL): Reducing Stress for Caregivers of Persons With Dementia, a Pilot Randomized Control Trial

Building on limitations of prior research, the investigators developed the Mindful and Self-Compassionate Care Program (MASC) to help caregivers of persons with Alzheimer Disease and Related Dementias (ADRD) manage stress associated with the general caregiver experience including stress stemming from managing challenging patient behaviors. MASC teaches: (1) mindfulness skills; (2) compassion and self-compassion skills; and (3) behavioral management skills. MASC also provides psychoeducation and group-based training and skill practice to facilitate skill uptake and integration within the caregiver experience and tasks.

The main aim is to: Demonstrate feasibility, acceptability, credibility, fidelity, preliminary efficacy and evidence for proposed mechanism of MASC through a pilot randomized controlled trial.

Relevant stakeholders (caregivers of persons with ADRD) will participate in the intervention.

Study Overview

Detailed Description

Over half of Alzheimer Disease and Related Dementias (ADRD) caregivers are actively looking for non-pharmacological interventions to decrease caregiver stress. Available programs do not sufficiently meet the psychological and practical needs of stressed caregivers of persons with ADRD; better solutions are needed. First, while helpful, most support groups do not systematically teach behavioral management skills which caregivers report needing in order to manage challenging patient behaviors. Second, behavioral management skills interventions exist, but do not teach: 1) emotional regulation skills which are necessary in order to foster caregiver ability to access and use these skills to manage patient behaviors, and/or 2) self-compassion and compassion skills which are necessary to bypass guilt and loneliness and navigate behavioral symptoms which are common caregiver challenges. Third, mindfulness and self-compassion interventions are effective solutions for managing stress, and distress across multiple populations, but engagement and efficacy among diverse ADRD caregivers are limited.

The guiding hypothesis of this proposal is that combining evidence-based mindfulness and self-compassion skills with behavioral management skills within a multi-component program increases intervention potency and efficiently supports caregivers of persons with ADRD. Accounting for practical challenges to engagement (number of sessions, delivery modality, skill practice) will also enhance uptake and reach.

The investigators will conduct an RCT study to explore feasibility benchmarks, target engagement and signal of improvement in stress, depression, anxiety and wellbeing (NIH stage 1B; N= up to 80 caregivers). The investigators will recruit caregivers of persons with ADRD from local community organizations and caregiver support programs; dementia research programs; and from national programs that focus on caregiving.

Study Type

Interventional

Enrollment (Estimated)

80

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • 18 years or older
  • English fluency and literacy
  • Meeting criteria for being a caregiver (e.g., family or friend of a care recipient who provides unpaid care)
  • Must live with and care for an individual with ADRD
  • Must have been in a caregiver role for more than 6 months
  • Must provide an average 4 hours of supervision or direct assistance per day for the are recipient
  • Perceived Stress Scale-4 (4-item) version >=6
  • Had managed 1 or more behavioral symptoms in past month

Exclusion Criteria:

  • Recent change in psychotropic treatment for depression or anxiety
  • Use of mindfulness apps or any meditation (more than 60 min/week in past 6 months)
  • Involvement in another clinical trial for caregivers, a score >= 4 on the Portable Mental Status Questionnaire (PMSQ)
  • No stated concerns or distress related to care recipient's disruptive behaviors
  • Involvement in another clinical trial for caregivers

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Single Group Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Mindful and Self-Compassionate Care Program (MASC)

The intervention arm will be comprised of:

Six Virtual Group Sessions. The sessions will teach mindfulness, self-compassion and behavioral management skills.

At Home Practice. After each group session, participants will have the opportunity to integrate the practices learned into their everyday life.

The intervention arm will be comprised of:

Six Virtual Group Sessions. The sessions will teach mindfulness, self-compassion and behavioral management skills.

At Home Practice. After each group session, participants will have the opportunity to integrate the practices learned into their everyday life.

Active Comparator: Health Education Program (HEP)

The control arm will be comprised of:

Six Virtual Group Sessions. The sessions will discuss caregiver stress, sleep hygiene, nutrition, and ways to stay physically active as a caregiver.

At Home Practice. After each group session, participants will have the opportunity to complete journal exercises that encourage them to integrate the health information that they learn into their daily lives.

The control arm will be comprised of:

Six Virtual Group Sessions. The sessions will discuss caregiver stress, sleep hygiene, nutrition, and ways to stay physically active as a caregiver.

At Home Practice. After each group session, participants will have the opportunity to complete journal exercises that encourage them to integrate the health information that they learn into their daily lives.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Satisfaction with the Intervention
Time Frame: Post-intervention (6-8 weeks post baseline)
The investigators will use the Client Satisfaction Questionnaire (CSQ-3) to assess participants' satisfaction with the intervention.
Post-intervention (6-8 weeks post baseline)
Feasibility of Recruitment
Time Frame: Baseline
The proportion of eligible participants who are eligible and choose to enroll in the study and the percentage of racial and ethnically diverse participants enrolled.
Baseline
Feasibility of Randomization
Time Frame: Baseline, Post intervention (6-8 weeks post baseline)
The percentage randomized who complete the post-test.
Baseline, Post intervention (6-8 weeks post baseline)
Feasibility of Assessment Measures
Time Frame: Baseline, Post-intervention (6-8 weeks post baseline), 3-months post intervention
The proportion of participants who complete the study with less than 25% of missing questionnaires.
Baseline, Post-intervention (6-8 weeks post baseline), 3-months post intervention
Feasibility of Quantitative Measures
Time Frame: Baseline, Post-intervention (6-8 weeks post baseline), 3-months post intervention
The benchmark of no questionnaires missing fully in ≥25% of caregivers.
Baseline, Post-intervention (6-8 weeks post baseline), 3-months post intervention
Adherence to treatment
Time Frame: Post-intervention
The proportion of caregivers who attend at least 4 out of the 6 sessions out of all randomized caregivers. Adherence to treatment will be estimated for both HEP and MASC.
Post-intervention
Patient's Global Impression of Change (PGIC)
Time Frame: Post-intervention (6-8 weeks post baseline)
PGIC is a 7-point scale depicting a participant's rating of overall improvement. Participants rate their change as "very much improved", "much improved", "minimally improved", "no change", "minimally worse", "much worse" or "very much worse"
Post-intervention (6-8 weeks post baseline)
Perceptions of Questionnaire Battery
Time Frame: Post-intervention (6-8 weeks post baseline)
The 'Perceptions of Questionnaire Battery' qualitative measure assesses how appropriately the participants fill the questionnaires, address their perception of stress, emotional distress and all other questionnaires.
Post-intervention (6-8 weeks post baseline)
Adherence to Home Practice
Time Frame: Weekly (up to 6 weeks
The proportion of participants who complete weekly home practice.
Weekly (up to 6 weeks
Perceptions of Email and Text Reminders
Time Frame: Post-intervention (6-8 weeks post baseline)
Participants' perception of emails and text messages reminders. The single question -, "Do participants think that the number of emails/texts received was: too little, just enough, too much?"
Post-intervention (6-8 weeks post baseline)
Credibility and Expectancy
Time Frame: Baseline
The Credibility and Expectancy Questionnaire (CEQ) assesses participants' perceptions that the treatment will work after participating in the intervention.
Baseline
Modified Perception of Global Improvement
Time Frame: (6-8 weeks post baseline)
The Modified Perception of Global Improvement (MPGI) is a global index designed to measure a participant's interpretation of changes in perceptions of stress following intervention.
(6-8 weeks post baseline)
Therapist Fidelity
Time Frame: Baseline through Post-intervention (6-8 weeks post baseline)
Ability of therapist to deliver the content of each session (through therapist completed adherence checklists) and therapist fidelity (through independent review of recorded sessions by Co-Investigator).
Baseline through Post-intervention (6-8 weeks post baseline)

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Symptoms of Depression
Time Frame: Baseline, Post-intervention (6-8 weeks post baseline), 3-months post intervention
Center for Epidemiological Studies-Depression Scale (CES-D). The CES-D is a 20-item scale widely used with ADRD participants. Response options range from 0 to 3 for each item (0 = Rarely or None of the Time, 1 = Some or Little of the Time, 2 = Moderately or Much of the time, 3 = Most or Almost All the Time) In scoring the CES-D, possible range of scores is 0 to 60, with the higher scores indicating the presence of more symptomatology.
Baseline, Post-intervention (6-8 weeks post baseline), 3-months post intervention
Mindfulness
Time Frame: Baseline, Post-intervention (6-8 weeks post baseline), 3-months post intervention
The Applied Mindfulness Process Scale (AMPS) is a process measure used to quantify how participants in mindfulness-based interventions (MBIs) use mindfulness practice when facing challenges in daily life. The AMPS yields 15 items representing three domains of applied mindfulness processes: (a) decentering, (b) positive emotional regulation, and (c) negative emotional regulation. AMPS can be scored by:(1) Adding each factor individually to obtain a score ranging from 0-20, and/or (2) adding all 15 items to obtain a score ranging from 0-60, with higher scores indicating higher use of mindfulness.
Baseline, Post-intervention (6-8 weeks post baseline), 3-months post intervention
Perceived Stress Scale
Time Frame: Baseline, Post-intervention (6-8 weeks post baseline), 3-months post intervention

The Perceived Stress Scale 10 (PSS-10) assesses perceived stress using a 5-point Likert scale.

The total score is determined by adding together the scores of each of the four items. Questions 2 and 3 are reverse coded. Questions 1 and 4: 0 = Never; 1 = Almost never; 2 = Sometimes; 3 = Fairly often; 4 = Very often Questions 2 and 3: 4 = Never; 3 = Almost never; 2 = Sometimes; 1 = Fairly often; 0 = Very often. Scores range from 0 to 40 with higher scores indicating more stress.

Baseline, Post-intervention (6-8 weeks post baseline), 3-months post intervention
Symptoms of Anxiety
Time Frame: Baseline, Post-intervention (6-8 weeks post baseline), 3-months post intervention
The State Trait Anxiety Inventory (STAI) state subscales (20 items) assesses anxiety symptoms in response to stressful situations. The range of possible scores varies from a minimum score of 20 to a maximum score of 80. STAI scores are commonly classified as "no or low anxiety" (20-37), "moderate anxiety" (38-44), and "high anxiety" (45-80).
Baseline, Post-intervention (6-8 weeks post baseline), 3-months post intervention
The Self-Compassion Scale
Time Frame: Baseline, Post-intervention (6-8 weeks post baseline), 3-months post intervention

The Self-Compassion Scale - Short Form (SCS-SF) is a 12-item self-report measure that is used by adults to measure their capacity for self-compassion - the ability to hold one's feelings of suffering with a sense of warmth, connection and concern. Self-Kindness Items: 2, 6 Self-Judgment Items (Reverse Scored): 11,

12 Common Humanity Items: 5, 10 Isolation Items: 4, 8 Mindfulness Items: 3, 7 Over-identification Items: 1, 9 = max score of 8 per category

Baseline, Post-intervention (6-8 weeks post baseline), 3-months post intervention
Compassion
Time Frame: Baseline, Post-intervention (6-8 weeks post baseline), 3-months post intervention
The Compassion Scale (CS) has 16 items assessing common humanity, kindness toward others and ability to understand the suffering or challenges of others. Kindness items: 2, 6, 10, 14 Common Humanity items: 4, 8, 12, 16 Mindfulness items: 1, 5, 9, 13 Indifference items (reverse scored): 3, 7, 11, 15. Subscale scores are computed by calculating the mean of the four subscale item responses. Total compassion scores are computed by reverse scoring the indifference items then taking a grand mean of all items. When examining subscale scores, higher scores on indifference items indicate less compassion before reverse-coding, and more compassion after reverse coding.
Baseline, Post-intervention (6-8 weeks post baseline), 3-months post intervention
Caregiver self-efficacy
Time Frame: Baseline, Post-intervention (6-8 weeks post baseline), 3-months post intervention
The Revised Caregiver Self-efficacy assesses domains of self-efficacy including obtaining respite, responding to disruptive patient behaviors and controlling upsetting through. The Caregiver Self-Efficacy Scale is an 8-item scale with possible scores ranging from 1 to 10 with higher scores indicating higher self-efficacy
Baseline, Post-intervention (6-8 weeks post baseline), 3-months post intervention
Loneliness
Time Frame: Baseline, Post-intervention (6-8 weeks post baseline), 3-months post intervention

The University of California, Los Angeles (UCLA) 3-item loneliness scale assesses relational connectedness, social connectedness and self-perceived isolation.

The scores for each individual question can be added together to give participants a possible range of scores from 3 to 9. Researchers in the past have grouped people who score 3 - 5 as "not lonely" and people with the score 6 - 9 as "lonely".

Baseline, Post-intervention (6-8 weeks post baseline), 3-months post intervention
Social Support
Time Frame: Baseline, Post-intervention (6-8 weeks post baseline), 3-months post intervention
The Interpersonal Support Evaluation List short form (ISEL) is a 12-item measure of perceptions of social support. Response options range from 1-4 with 4 = "definitely true" if the participant is sure it is true about them, 3= "probably true" if the participant thinks it is true but is not absolutely certain. Similarly, the participant should circle 1 = "definitely false" if they are sure the statement is false and 2 = "probably false" if the participant thinks it is false but is not absolutely certain. This questionnaire has three different subscales designed to measure three dimensions of perceived social support. These dimensions are: 1.) Appraisal Support 2.) Belonging Support 3.) Tangible Support Each dimension is measured by 4 items on a 4-point scale ranging from "Definitely True" to "Definitely False". Scores range from 4-16.
Baseline, Post-intervention (6-8 weeks post baseline), 3-months post intervention
Well-being
Time Frame: Baseline, Post-intervention (6-8 weeks post baseline), 3-months post intervention
The World Health Organization-Five Well-Being Index (WHO-D) has 5 items assessing emotional well-being. The raw score is calculated by totaling the figures of the five answers. The raw score ranges from 0 to 25, 0 representing worst possible and 25 representing best possible quality of life. To obtain a percentage score ranging from 0 to 100, the raw score is multiplied by 4. A percentage score of 0 represents the worst possible, whereas a score of 100 represents the best possible quality of life
Baseline, Post-intervention (6-8 weeks post baseline), 3-months post intervention
Distress Due to Patient Challenges Behaviors
Time Frame: Baseline, Post-intervention (6-8 weeks post baseline), 3-months post intervention
The Neuropsychiatric Inventory Caregiver Distress Scale has 12 items assessing distress associated with dementia patient's behaviors such as apathy, elation, disinhibition. Participant distress is rated for each positive neuropsychiatric symptom domain on a scale anchored by score from 0 to 5 points. The Score is: 0 = Not distressing at all, 1 = Minimal (slightly distressing, not a problem to cope with), 2 = Mild (not very distressing, generally easy to cope with), 3 = Moderate (fairly distressing, not always easy to cope with), 4 = Severe (very distressing, difficult to cope with), 5 = Extreme of Very Severe (extremely distressing, unable to cope with)
Baseline, Post-intervention (6-8 weeks post baseline), 3-months post intervention
Dyadic Relationship Scale
Time Frame: Baseline, Post-intervention (6-8 weeks post baseline), 3-months post intervention
The Dyadic Relationship Scale (DRS) (11 items) assesses negative and positive dyadic interactions between caregivers and their care recipient. Each item is rated on four-point scale (0-3) and responses are summed for a total score. Possible scores range from 0 to 33 with higher scores indicating higher levels of strain and positive interaction.
Baseline, Post-intervention (6-8 weeks post baseline), 3-months post intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Ana-Maria Vranceanu, PhD, Massachusetts General Hospital
  • Principal Investigator: Christine Ritchie, MD, MSPH, Massachusetts General Hospital

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 22, 2024

Primary Completion (Estimated)

March 15, 2025

Study Completion (Estimated)

April 1, 2025

Study Registration Dates

First Submitted

February 18, 2024

First Submitted That Met QC Criteria

February 18, 2024

First Posted (Actual)

February 23, 2024

Study Record Updates

Last Update Posted (Actual)

March 25, 2024

Last Update Submitted That Met QC Criteria

March 22, 2024

Last Verified

March 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • 2023P003638
  • 1R01AG078204-01 (U.S. NIH Grant/Contract)

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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