Mobile Tablet Education to Advance Caregiver Health

Dementia Clinical Trial

— MTEACHing  

Official title:

Mobile Media Intervention for Family Caregivers of Veterans With Dementia

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03417219
• Other study ID #: E1710-P
• Secondary ID: 1I21RX001710
• Status: Completed
• Phase: N/A
• Start date: January 1, 2015
• Est. completion date: June 30, 2018

Study information

• Verified date: January 2019
• Source: VA Office of Research and Development
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

To address the high burden of caring for a Veteran with dementia, the investigators propose to study the effect of a low-cost, rehabilitative intervention for family caregivers of Veterans with dementia. The investigators' novel approach will use mobile media technology that can reach caregivers in rural areas who do not have easy access to major VA medical centers. If this rehabilitative intervention proves successful, it may represent an approach to Veteran and family-centered dementia care that can be used throughout VA with low staff, resource, and cost burdens.

Description:

The proposed project studies the effects of an education and skill-building rehabilitation intervention, designed to be low-cost and clinically translatable through mobile media devices (i.e., tablets), on family caregivers of Veterans with dementia. Intervention effects will be examined longitudinally at baseline and 3 months post-intervention.

Advanced statistical techniques will be used to determine the impact of the intervention on:

quality of life in caregivers of Veterans with dementia (Aim 1), perceived stress and depressive symptoms in caregivers (Aim 2), and socialization and engagement in pleasant activities in caregivers (Aim 3).

If this rehabilitative intervention proves successful, it may represent an approach to Veteran- and family-centered dementia care that can be used throughout VA with low staff, resource, and cost burdens.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 16
• Est. completion date: June 30, 2018
• Est. primary completion date: December 31, 2017
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

-- Participants must:

• report distress associated with being the primary caregiver for a family member with dementia

• reporting at least 2 of the following 6 items at baseline assessment: felt overwhelmed, felt like they often needed to cry, were angry or frustrated, felt they were cut off from family or friends, reported moderate to high levels of general stress, or felt their health had declined

• provide at least 7 hours of care (supervision or direct assistance) per week over the past 3 months (other sources of caregiving for the Veteran with dementia can also be utilized; e.g., respite, home health aide, other family members)

• cohabitate with a Veteran diagnosed with dementia

• be proficient in spoken and written English

• be capable of providing informed consent

Exclusion Criteria:

-- Potential participants will be screened and excluded for:

• current or lifetime history of any psychiatric disorder with psychotic features

• prominent suicidal or homicidal ideation

• having met DSM-IV criteria for drug or alcohol abuse or dependence (except nicotine) within the past six months

• presence of alcohol intoxication (by breathalyzer) or alcohol withdrawal (by exam) during study recruitment or participation

• diagnosis of probable or possible dementia

• a Telephone Cognitive Screen score of < 20

• participation in another caregiver intervention study within the past year

• lack of access to telephone and internet services in the home

• illness that would prevent study participation

• planned transfer of care receiver to another caregiver or nursing home within 6 months

• currently living with an implantable cardioverter defibrillator or pacemaker

• known pregnancy at time of consent

Related Conditions & MeSH terms

• Dementia

Intervention

Behavioral:
• Education and Skill Building Rehabilitation-mobile (ESBR-m)
Participants randomized to the ESBR-m group will participate in four, 90-minute group ( 5 participants) sessions. These four sessions are supplemented with a booster session one month following the last intervention session.
• Usual Care (UC)
Participants randomized to the UC group will receive supplemental educational materials (e.g., VA Caregiver Support Program; Veterans Crisis Line; National Institute on Aging's "Understanding Memory Loss").

Locations

Country	Name	City	State
United States	VA Palo Alto Health Care System, Palo Alto, CA	Palo Alto	California

Sponsors (1)

Lead Sponsor	Collaborator
VA Office of Research and Development

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change From Baseline Zarit Burden Interview (ZBI) at 4 Months	The Zarit Burden Interview (ZBI) is a 22-item self-report measure of caregiver burden. Several version of the ZBI have been used successfully as outcome measures in interventions for dementia caregivers. Scores for each item range from 0 (never) to 4 (nearly always) on questions such as "Do you feel embarrassed by your relative's behavior?." Total scores are calculated by summing all responses and range from 0-88. A higher score is indicative of a worse outcome.	Baseline, 4 month follow-up
Primary	Change From Baseline Center for Epidemiological Studies-Depression (CES-D) at 4 Months	The Center for Epidemiological Studies-Depression (CES-D) is a 20-item, self-report measure of frequency of depressive symptoms over a one week period. The CES-D is frequently used to assess depression in dementia caregivers and has been shown to be sensitive to changes in caregiver depression post intervention. Scores for each item range from 0 (rarely or none of the time) to 3 (most or all of the time), with some items reverse coded. Total scores are calculated by summing all responses and range from 0-60. A higher score is indicative of a worse outcome.	Baseline, 4 month follow-up
Primary	Change From Baseline Perceived Stress Scale (PSS) at 4 Months	The Perceived Stress Scale (PSS) is the most widely used psychological instrument for measuring the perception of stress. It is a measure of the degree to which situations in one's life are appraised as stressful. Items were designed to tap how unpredictable, uncontrollable, and overloaded respondents find their lives. The scale also includes a number of direct queries about current levels of experienced stress. We use a 14 item version of the PSS with a minimum score of 0 and a maximum score of 56. Lower values indicate lower perceived stress while higher values indicate higher perceived stress.	Baseline, 4 month follow-up