WEB-BASED SUPPORT PROGRAM FOR CAREGIVERS OF VETERANS WITH DEMENTIA DISCHARGED FROM SKILLED NURSING FACILITIES TO HOME

The goal of this clinical trial is to learn whether an evidence-based caregiver support program (Hospital GamePlan4Care) can benefit caregivers of hospitalized Veterans with Alzheimer's Disease and Related Dementia who are discharged to skilled nursing facilities prior to returning home. The main questions it aims to answer are:

• Is Hospital GamePlan4Care feasible and acceptable to caregivers?
• Does Hospital GamePlan4Care improve caregiver-reported outcomes?

Researchers will compare Hospital GamePlan4Care to health education to see if it improves caregiver reported outcomes.

Participants in the Hospital GamePlan4Care arm will receive tailored skills training and support. Participants will be asked to:

• Complete tailored skills training on the Hospital GamePlan4Care website
• Complete four phone calls with a dementia care specialist to receive tailored training and support
• Complete questionnaires at enrollment, one month, and three months after enrollment.
• Complete an interview at three months

Participants in the health education arm will receive education materials for caregivers. Participants will be asked to:

• Review the education materials
• Complete four phone calls with a dementia care specialist to review the materials
• Complete questionnaires at enrollment, one month, and three months after enrollment.

Study Overview

• Status: Not yet recruiting
• Conditions: Caregivers
• Intervention / Treatment: Other: Health Education; Behavioral: Hospital GamePlan4Care

Detailed Description

Hospital GamePlan4Care is an evidence-informed intervention designed to support caregivers of hospitalized adults with dementia. Hospital GamePlan4Care was developed and tested with feedback from caregivers and health professionals and found to be feasible and acceptable to caregivers in a single arm pilot study. Hospitalization of an adult with dementia can be associated with negative outcomes for the adult with dementia (e.g., cognitive decline, functional decline) and caregivers (e.g., depression, increased stress), which may place the adult with dementia at increased risk for elder mistreatment following hospital discharge. Supporting caregivers during care transitions may improve outcomes for caregivers and mediate the risk for elder mistreatment. This clinical trial addresses an important gap in our understanding of the potential benefits of caregiver-support programs during care transitions for caregivers and adults with dementia.

This study will be a non-blinded randomized study comparing Hospital GamePlan4Care (intervention arm) to a Health Education (control arm) for caregivers of hospitalized Veterans with dementia who are discharged to a skilled nursing facility prior to returning home. Caregivers of adults with dementia will be recruited while the Veteran is admitted to a skilled nursing facility after hospital discharge. Following baseline data collection, enrolled caregivers will be randomized to Hospital GamePlan4Care or Caregiver Education arm in a 1:1 ratio using the randomization feature in VA REDCap. Each arm will continue for three months after the caregiver is enrolled. The primary outcomes are caregiver-reported and will be measured 30 days and 90 days after caregiver enrollment.

• Study Type: Interventional
• Enrollment (Estimated): 55
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: Molly Horstman, MD, MS; Phone Number: 234642 713-440-4400; Email: molly.horstman1@va.gov
• Study Contact Backup: Name: Timothy Zhou, MA; Phone Number: (713) 794-7939; Email: Timothy.Zhou@va.gov

Study Locations

• United States
  • Texas
    • Houston, Texas, United States, 77030
      • Michael E. DeBakey VA Medical Center
      • Contact: Molly Horstman, MD, MS; Phone Number: 234642 713-440-4400; Email: molly.horstman1@va.gov
      • Principal Investigator: Molly Horstman, MD, MS

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult; Older Adult
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

• 18 years of age or older
• provide care for a Veteran with a diagnosis of Alzheimer's Disease or related dementias or a Veteran with a prescription for a medication for dementia listed in CPRS who is admitted to the hospital at the Michael E. DeBakey VA Medical Center
• Veteran must be experiencing signs of dementia as verified by a score of 2 or greater on the AD-8
• care for a Veteran with dementia who is discharged to a VA or non-VA skilled nursing facility prior to returning home
• provide at least eight hours of care or supervision per week to the Veteran with dementia
• provide care primarily due to a personal relationship, rather than a financial relationship
• have access to a telephone
• have access to a tablet or computer with internet access
• report using the computer or tablet to access the internet at least three times per week
• speak English

Exclusion Criteria:

• unable to complete informed consent

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Supportive Care
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: None (Open Label)

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Active Comparator: Health Education; Education on general caregiving topics.	Other: Health Education; Caregivers in the health education arm will receive a VA Care Transitions Handbook, 4 emails with a weblink to a general caregiving topic, and 4 phone calls to confirm that the emails were received over a 3-month period.
Experimental: Hospital GamePlan4Care; Tailored caregiver skills training and support for caregiving for a person with dementia	Behavioral: Hospital GamePlan4Care; The Hospital GamePlan4Care intervention will include access to a written VA Care Transitions handbook, access to the GamePlan4Care website for skills training, 11 emails encouraging them to visit the website, and four phone calls with a dementia care specialist to tailor the training to the caregiver's needs over a 3-month period

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Caregiver Unmet Needs: Benjamin Rose Unmet Needs Scale	The Benjamin Rose Institute Unmet Need Scale includes 39 yes/no questions about different need that caregivers have (no=0, yes=1). The total score is a sum of all the yes responses. Higher scores indicate higher unmet needs.	Baseline, 30 days and 90 days

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change in Zarit Caregiving Burden Interview (12-item)	Each item represents a statement related to an aspect of perceived burden. All questions are answered as never (0 points), rarely (1 point), sometimes (2 points), quite frequently (3 points), or nearly always (4 points). A total score will be obtained by summing all items with higher scores indicating higher rates of burden (range: 0-48).	Baseline, 30 days and 90 days
Change in Center for Epidemiological Studies Depression Scale (CES-D) (10-item)	The CES-D provides a list of feelings and behaviors. For each item, respondents report how often they have felt that way in the past week with each item receiving a score from 0-3. A total score will be obtained by summing scores for all items with higher scores indicating higher levels of depressed symptoms (range: 0-30).	Baseline, 30 days, and 90 days
Change in Self-Rated Health (1-item)	The investigators will use the single self-rated health item: "In general, would you say your health is:" with response options of Excellent, Very Good, Good, Fair, and Poor	Baseline, 30 days, and 90 days
Change in Self-Efficacy for Caregiving (CSES-8)	The CSES-8 asks questions about confidence in being able to manage different caregiving situations. Each question is rated on a 1 (not at all confident) to 10 (totally confident scale). The score of the scale is the mean of the eight items. Higher scores indicate greater self-efficacy.	Baseline, 30 days, and 90 days
Change in Caregiver Distress on the Neuropsychiatric Inventory Questionnaire	The Neuropsychiatric Inventory Questionnaire includes a list of 12 symptoms (e.g. delusions, hallucinations, agitation/aggression). For each symptom, the caregiver responds if the symptom was present in the past month (yes/no) and the level of distress the caregiver feels due to that symptom (0-5). Higher scores indicate greater distress due to that symptom.	Baseline, 30 days, and 90 days
Neglect and Aggression Questionnaire	Questions adapted from the Conflict Tactics Scale Revised and CTS2 modified for older adults; Conflict Tactics Scale for Child Mistreatment; and prior research (Pickering 2024, PMID 39136354). Asks how often the caregiver or care recipient has done I something in the past month. Questions include neglect of the care recipient, caregiver self-neglect, physical and psychological aggression of the caregiver to the care recipient, and physical and psychological aggression of the care recipient to the caregiver.	Baseline, 30 days, and 90 days

Collaborators and Investigators

• Sponsor: Baylor College of Medicine
• Collaborators: The University of Texas Health Science Center, Houston; National Institute on Aging (NIA)

Study record dates

Study Major Dates

• Study Start (Estimated): February 17, 2026
• Primary Completion (Estimated): February 17, 2027
• Study Completion (Estimated): February 17, 2027

Study Registration Dates

• First Submitted: January 28, 2026
• First Submitted That Met QC Criteria: January 28, 2026
• First Posted (Actual): February 4, 2026

Study Record Updates

• Last Update Posted (Actual): February 4, 2026
• Last Update Submitted That Met QC Criteria: January 28, 2026
• Last Verified: January 1, 2026

More Information

Terms related to this study

• Other Study ID Numbers: H-55864; 5P30AG086563-02 (U.S. NIH Grant/Contract)

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: YES
• IPD Plan Description: The investigators will provide a de-identified dataset compliant with VA data security policy to the public upon request to the principal investigator.
• IPD Sharing Time Frame: After the data is analyzed and published

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No