A Non-pharmacological Intervention for Patients With Alzheimer's Disease and Family Caregivers (Care Partners Program)

Caregiver Clinical Trial

— CPProgram  

Official title:

Dual Target Program: An Non-pharmacological Intervention for Family Caregivers and Patients With Alzheimer's Disease

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03333252
• Other study ID #: 1803019068
• Secondary ID: 5R01AG054009
• Status: Completed
• Phase: N/A
• Start date: January 29, 2018
• Est. completion date: May 1, 2023

Study information

• Verified date: March 2024
• Source: Weill Medical College of Cornell University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The proposed study will develop and test the efficacy and feasibility of a dyadic-based intervention program (DT), delivered through state-of-the art computer tablet technology. A novel feature of the investigation is its focus on both the caregiver and the recipient of care (person with AD) and the integration of an evidenced-based caregiver intervention and evidenced-based cognitive/functional training for the care recipient. The program will be tailored for the caregiver and emphasize issues important to caregivers, not only in the earlier stages of caregiving, but will also target issues across the caregiving trajectory to help prepare the caregiver for changes in their role. Two hundred and forty Hispanic, African American and White/Caucasian dyads will be randomized to the DT intervention or Control condition. Measures at baseline and the 6 and 12-month follow-ups will include indices of care recipient processing speed and quality of life, and caregiver outcomes such as; depression, burden, self-care activities and social support . Information will also be gathered on ethnic differences in response to the intervention and estimates of cost effectiveness of the intervention.

Description:

We will recruit and randomly assign, following a baseline assessment, 246 dyads will be enrolled and randomly assigned to one of two groups: 1) Caregiving Condition or 2) Health Promotion (Nutrition) Condition. The entire study is home-based. The intervention will be delivered over 6 months using computer tablet technology in Spanish or English. Assessments will occur in the beginning of the study, 6 months, and 12 months (after completion of the intervention)

Interested participants (caregivers) can contact us via telephone or email after seeing a flyer posted in various WCM/NYP locations including the Irving Sherwood Wright Center on Aging. One of our research associates (RA) will provide more information about the study to potential participants. The trained RA will use a telephone script with consent language to obtain permission to ask them questions to determine their eligibility through a phone screen script. If the participant is ineligible for the study, all screening data will be deleted. If the caregiver participant is eligible for the study, an appointment will be provided, and one of our RAs will visit the participants (caregiver and care recipient) and conduct the baseline assessment at the participants' home in their preferred language (Spanish or English). This assessment with the caregiver will last between 2 and 3 hours, additionally the assessment with the care recipient will last approximately 1.5 hours. We will use Qualtrics (online survey/data collection service) to administer the assessments.

The baseline assessment with the caregiver (CG) consists of a series of questionnaires assessing the level of burden, and depression perceived by the CG while providing the care, the amount of social support available to the CG, and the self-care activities of the CG to provide continuing care to their loved ones. The assessment with the care recipient consists of measures of processing speed (digit symbol). In addition, the care recipient will complete a computer-based questionnaire assessing their quality of life. The assessment with the caregiver and care recipient might not be completed in the same home visit. The study protocol allows multiple visits to complete the assessments.

During the baseline home visit, the RA will go over the written informed consent and HIPAA authorization with the participants (caregiver and care recipient). The assessment will not begin unless the participant has a full understanding of the informed consent form and has signed the form. The care recipient will additionally be given a Consent Feedback Tool, as an added step to make sure they understand the consent form since they have mild cognitive impairment.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 352
• Est. completion date: May 1, 2023
• Est. primary completion date: May 1, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 21 Years and older

Eligibility

CAREGIVER (CG)

Inclusion Criteria:

• MMSE = 26 (with Mungus age and education correction)

• Providing care for a friend or relative with AD for a minimum of eight hours per week for at least the past six months

• Being over the age of 21 years

• Living with or nearby the patient

• Having a telephone

• Planning to stay in the study geographic area for the duration of the study

Exclusion Criteria:

• Not providing care to someone with memory problems

• Paid caregivers

• Has terminal illness with life expectancy of 6 months or less

CARE RECIPIENT (CR)

Inclusion Criteria:

• MMSE 18 - 25 (with Mungus age and education correction) (if scores high on MMSE, the care recipient has to score 1.0 in the Clinical Dementia Rating Scale (CDR))

• Needs help with higher level of IADL (e.g., managing finances, helping remember appointments, handling medications)

• Show memory problems

Exclusion Criteria:

• Lives in nursing home or facility

• Going to be placed in a facility in the next 6 months

• Has terminal illness with life expectancy of 6 months or less

Related Conditions & MeSH terms

• Alzheimer Disease
• Caregiver

Intervention

Behavioral:
• Intervention Condition
Caregivers will access caregiving related information. Care Recipients will access cognitive training program
• Control Condition
Caregivers will access Nutrition and Health Promotion material. Care Recipients will access words and card games

Locations

Country	Name	City	State
United States	University of Miami Miller School of Medicine	Miami	Florida
United States	Weill Cornell Medicine	New York	New York

Sponsors (2)

Lead Sponsor	Collaborator
Weill Medical College of Cornell University	National Institute on Aging (NIA)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Change in Caregiver's Self Report of Self-care	Higher score means better in keeping medical obligations to him/herself. Range (0-12)	Baseline, 6-mth follow-up and 12-mth follow-up
Other	Change in Caregiver's Social Support	Higher score means more social support for the caregiver. Range (0-40)	Baseline, 6-mth follow-up and 12-mth follow-up
Other	Change in Care Recipient's Qualify of Life	Higher score means better quality of life as Alzheimer's patient. Range (0-52)	Baseline, 6-mth follow-up, and 12-mth follow-up
Other	Change in Care Recipient's Processing Speed Using Digit Symbol Test	Higher score means faster processing speed. Range (0-100)	Baseline, 6-mth follow-up, and 12-mth follow-up
Primary	Change in Depression Score for Caregiver as Measured by CES-D	Higher score on the Center for Epidemiological Studies Depression scale (CES-D) means greater frequency of depressive symptoms. Range (0-30)	Baseline, 6-mth follow-up and 12-mth follow-up
Secondary	Change in Caregiving Burden Score for Caregiver as Measured by Burden Inventory	Higher score means greater level of caregiver burden. Range (0-44)	Baseline, 6-mth follow-up and 12-mth follow-up