Social-Life Enhancing Activities for Caregivers

November 9, 2023 updated by: Benzi Kluger, MD, University of Rochester

Improving Care Partner Outcomes Through Positive Connections

This study examines a behavioral intervention to improve social connection and reduce loneliness for caregivers of a loved one with Dementia with Lewy Bodies (DLB). The intervention is called Social LEAF. The objective is to examine psychological mechanisms whereby Social LEAF delivered in a group and via video call reduces loneliness and improves positive emotions for older caregivers of loved ones with DLB. This is an 18-month Stage 2 study examining Social LEAF, which is strengths-based and teaches positive coping skills focused on improving social relationships and is delivered remotely in a group format. These two adaptations to the original LEAF intervention are included to provide a more potent means of improving social connection. A pilot phase with 20 caregivers (Aim 1) will address these adaptations regarding feasibility, acceptability, and signal for reducing loneliness, with refinements as needed. A second phase (Aims 2 and 3) will involve a randomized trial comparing Social LEAF to control (30 caregivers in each arm) on loneliness (primary outcome), positive affect (mechanism), and social engagement (mechanism). Data will also be collected on acceptability and perceived benefits using mixed methods.

Aim 1 is to refine the LEAF intervention to target social relationships and loneliness.

Aim 2 is to examine feasibility and acceptability of Social LEAF for DLB caregivers.

Aim 3 is to examine efficacy of Social LEAF in reducing loneliness, increasing positive affect, and increasing social engagement.

Study Overview

Status

Completed

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

61

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 Locations

    • New York
      • Rochester, New York, United States, 14642
        • University of Rochester

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

50 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion criteria:

  • Must be a primary care partner of a person that has been clinically diagnosed with Dementia with Lewy Bodies (DLB) or Parkinson's Disease Dementia, and has access to high-speed internet connection at home or in a location where they can speak privately with a facilitator. iPads and a hotspot will be given to those who lack internet and a sufficient mobile device but show willingness to participate. The iPads and hotspot will be returned to the study team once study procedures have concluded. Must be willing and ready to begin the intervention either immediately or in 6 weeks depending on which group they are randomly selected to be in.
  • Must begin LEAF procedures as soon as consented to the study. Has not taken part in Aim 1 of the study.
  • Will have waited the 6-week period before starting LEAF procedures after consenting and has not taken part in Aim 1 of the study.

Exclusion:

  • Not a primary care partner of a person with DLB. Is a primary care partner of someone who has not been clinically diagnosed with DLB. Cannot speak English or provide clear and concise consent to the project.
  • Has not started LEAF procedures at the beginning and has taken part in Aim 1 of the study.
  • Has started/taken part in the LEAF procedures at the beginning and also has taken part in Aim 1 of the study.

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: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Aim 1
Experimental: Aim 2
We will be utilizing the Life Enhancing Activities or Caregivers (LEAF) intervention to display that social networks' can be used as a means of reinforcing the positive life skills of the intervention; and that these same skills will enhance social networks, increase mutual satisfaction in social interactions, and boost motivation to reach out to others, thus combatting social isolation.
Social LEAF is an adaptation of the Life Enhancing Activities for Family Caregivers program to focus on social relationships and loneliness. Social LEAF is a six-session group program provided by video-conference that teaches caregivers coping skills to improve social relationships and social connection. Social LEAF is delivered in groups of up to 10 caregivers via videoconference and will consist of six weekly hour-long discussion-based classes to teach positive coping skills around improving social relationships. Each week will focus on a skill from the original LEAF study adapted to the group and social context.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Loneliness (UCLA Loneliness Scale)
Time Frame: Week 6
The UCLA Loneliness scale produces a continuous score of the degree to which participants endorse loneliness, which higher scores indicating greater loneliness.
Week 6
Loneliness (UCLA Loneliness Scale)
Time Frame: Week 12
The UCLA Loneliness scale produces a continuous score of the degree to which participants endorse loneliness, which higher scores indicating greater loneliness.
Week 12

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Positive emotions (Modified Differential Emotions Scale)
Time Frame: Week 6
The Modified Differential Emotions Scale, positive emotions subscale, assesses the frequency of experiencing positive emotions over the past week, with higher scores indicating greater frequency of positive emotions in the past week (range 1-4).
Week 6
Positive emotions (Modified Differential Emotions Scale)
Time Frame: Week 12
The Modified Differential Emotions Scale, positive emotions subscale, assesses the frequency of experiencing positive emotions over the past week, with higher scores indicating greater frequency of positive emotions in the past week (range 1-4).
Week 12
Positive aspects of caregiving (Positive Aspects of Caregiving scale)
Time Frame: Week 6
The Positive Aspects of Caregiving Scale consists of nine items assessing positive consequences of caregiving, each rated on a 1-5 Likert scale (range of scores 9-45), with a higher score reflects a more positive perception of the caregiving experience.
Week 6
Positive aspects of caregiving (Positive Aspects of Caregiving scale)
Time Frame: Week 12
The Positive Aspects of Caregiving Scale consists of nine items assessing positive consequences of caregiving, each rated on a 1-5 Likert scale (range of scores 9-45), with a higher score reflects a more positive perception of the caregiving experience.
Week 12
Social engagement (Social Engagement and Activities Questionnaire; SEAQ)
Time Frame: Week 6
The SEAQ measures the frequency during the past month of ten social activities, and yields a total score ranging from 0 (no engagement in any of the ten activities) to 50 (daily engagement in all ten activities).
Week 6
Social engagement (Social Engagement and Activities Questionnaire; SEAQ)
Time Frame: Week 12
The SEAQ measures the frequency during the past month of ten social activities, and yields a total score ranging from 0 (no engagement in any of the ten activities) to 50 (daily engagement in all ten activities).
Week 12

Collaborators and Investigators

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

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)

July 28, 2022

Primary Completion (Actual)

July 23, 2023

Study Completion (Actual)

July 23, 2023

Study Registration Dates

First Submitted

January 27, 2022

First Submitted That Met QC Criteria

March 1, 2022

First Posted (Actual)

March 10, 2022

Study Record Updates

Last Update Posted (Actual)

November 14, 2023

Last Update Submitted That Met QC Criteria

November 9, 2023

Last Verified

November 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • 375254
  • P30AG064103 (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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