Caregiver Speaks: A Technologically Mediated Storytelling Intervention
Primary Purpose
Alzheimer Disease
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Photo elicitation
Sponsored by
About this trial
This is an interventional supportive care trial for Alzheimer Disease
Eligibility Criteria
Inclusion Criteria:
- be a designated family caregiver (i.e., a family member or friend providing unpaid care) of a PLWD who is enrolled in hospice care,
- be at least 18 years old,
- be involved in decisions related to their loved one's hospice care,
- have access to a digital camera or other photo-taking device such as a cell phone
- be willing to photograph images they feel capture their caregiving and bereavement experiences
- be willing to set up a Facebook account and join the private Facebook group, 7) have access to e-mail for REDCap survey data collection
Exclusion Criteria:
- none
Sites / Locations
- University of Missouri
Arms of the Study
Arm 1
Arm 2
Arm Type
No Intervention
Experimental
Arm Label
Control
Intervention
Arm Description
Will receive usual hospice care plus measures
Will receive photo elicitation intervention and will join a secret Facebook group to share photos with other caregivers
Outcomes
Primary Outcome Measures
Change in Public Health Questionaire- 9 depression score
Caregiver depression measure.Response options range from 0 (not at all) to 3 (nearly every day), with total scores ranging from 0 to 27. Higer scores indicate more depression.
Secondary Outcome Measures
Change in General Anxiety Disorder -7 anxiety score
Caregiver anxietyResponse options range from 0 (not at all) to 3 (nearly every day), with total scores ranging from 0 to 21. Total scores of 5, 10, and 15 represent thresholds for mild, moderate, and severe anxiety, respectively. Total scores of 10 or higher are generally considered clinically significant, signaling a need for additional evaluation and possible intervention
Full Information
NCT ID
NCT04103580
First Posted
July 25, 2019
Last Updated
September 26, 2023
Sponsor
Washington University School of Medicine
1. Study Identification
Unique Protocol Identification Number
NCT04103580
Brief Title
Caregiver Speaks: A Technologically Mediated Storytelling Intervention
Official Title
Caregiver Speaks: A Technologically Mediated Storytelling Intervention for Family Caregivers of Individuals With Alzheimer's Disease and Other Dementias
Study Type
Interventional
2. Study Status
Record Verification Date
September 2023
Overall Recruitment Status
Completed
Study Start Date
March 1, 2020 (Actual)
Primary Completion Date
July 17, 2023 (Actual)
Study Completion Date
August 1, 2023 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Washington University School of Medicine
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
Caregiver speaks is a randomized trial of a Photo elicitation intervention for caregivers of Alzheimers patients.
Detailed Description
This randomized controlled trial will test an intervention for an understudied population - family caregivers of persons living with dementia (PLWD). This project is the first of its kind to longitudinally follow family caregivers of PLWD into bereavement. Furthermore, the intervention, Caregiver Speaks, employs an innovative storytelling approach - photo elicitation (the use of photos to elicit thoughts, feelings, and reactions to a person's experience) - to encourage family caregivers to make meaning of their caregiving and bereavement experiences as a way of reducing depression, anxiety, and ultimately grief intensity. Caregiver Speaks is deployed via a readily available social media network (Facebook), which allows easy access for already overburdened family caregivers of PLWD, and can improve their social support. Preliminary work demonstrates that 1) this project is feasible as an RCT intervention study of caregiver experiences, 2) the research team can conduct this type of storytelling intervention via Facebook, and 3) family caregivers use (and want to use) social media during active caregiving and into bereavement, despite their heavy care burdens. The research team will base the proposal on Park and Folkman's meaning-making model of stress and coping. This model illustrates how individuals cope with adverse life events (i.e., trauma, or death of a loved one) by reconstructing and transforming the event's meaning and incorporating the reappraised meaning into one's larger self-narrative. Caregiver Speaks uses storytelling in the form of photo-elicitation, in order to facilitate this meaning-making. Caregivers share photos and discussions regarding their caregiving and bereavement experiences in a private, facilitated Facebook group. This model suggests that caregivers' ability to make sense of (meaning making), and find benefit in an adverse life situation (caregiving and bereavement) will be validated through social support, and result in reduced depression, anxiety, and grief intensity. Caregivers will be randomly assigned to either: 1) Group 1, which will receive the Caregiver Speaks intervention, or 2) Group 2, which will receive standard care, including the standard care for bereavement. The research team will use both quantitative and qualitative methods in parallel and equal status to measure the intervention's efficacy. The overall hypothesis is that participating in Caregiver Speaks during caregiving and into bereavement will reduce caregivers' depression and anxiety, and as a result will reduce grief intensity in bereavement. The three specific aims are to: 1) determine the efficacy of the Caregiver Speaks intervention in reducing depression and anxiety among family caregivers of people with dementia, 2) examine the intervention's effect on grief intensity among bereaved family caregivers of people with dementia, and 3) describe how caregivers made meaning of their caregiving and bereavement experiences.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Alzheimer Disease
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomized 2 arm study; control and intervention
Masking
None (Open Label)
Allocation
Randomized
Enrollment
457 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Control
Arm Type
No Intervention
Arm Description
Will receive usual hospice care plus measures
Arm Title
Intervention
Arm Type
Experimental
Arm Description
Will receive photo elicitation intervention and will join a secret Facebook group to share photos with other caregivers
Intervention Type
Behavioral
Intervention Name(s)
Photo elicitation
Intervention Description
Caregivers are taught to use photos to illustrate various feelings and meanings
Primary Outcome Measure Information:
Title
Change in Public Health Questionaire- 9 depression score
Description
Caregiver depression measure.Response options range from 0 (not at all) to 3 (nearly every day), with total scores ranging from 0 to 27. Higer scores indicate more depression.
Time Frame
Baseline and twelve months
Secondary Outcome Measure Information:
Title
Change in General Anxiety Disorder -7 anxiety score
Description
Caregiver anxietyResponse options range from 0 (not at all) to 3 (nearly every day), with total scores ranging from 0 to 21. Total scores of 5, 10, and 15 represent thresholds for mild, moderate, and severe anxiety, respectively. Total scores of 10 or higher are generally considered clinically significant, signaling a need for additional evaluation and possible intervention
Time Frame
Baseline and twelve months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
be a designated family caregiver (i.e., a family member or friend providing unpaid care) of a PLWD who is enrolled in hospice care,
be at least 18 years old,
be involved in decisions related to their loved one's hospice care,
have access to a digital camera or other photo-taking device such as a cell phone
be willing to photograph images they feel capture their caregiving and bereavement experiences
be willing to set up a Facebook account and join the private Facebook group, 7) have access to e-mail for REDCap survey data collection
Exclusion Criteria:
none
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Debra Parker Oliver, PhD
Organizational Affiliation
Washington University School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Missouri
City
Columbia
State/Province
Missouri
ZIP/Postal Code
65202
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
No individual data will be shared
Learn more about this trial
Caregiver Speaks: A Technologically Mediated Storytelling Intervention
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