IN-HOME: Testing Preliminary Effectiveness of a CHW Training Program to Support African American and Latino Male Caregivers

Sponsor
KDH Research & Communication (Industry)
Overall Status
Completed
CT.gov ID
NCT06049043
Collaborator
(none)
122
1
2
3.3
36.8

Study Details

Study Description

Brief Summary

Two arm study, experimental and control, to explore the impact of an online training program to prepare community health workers conduct effective outreach to support African American and Latino male caregivers of older adults.

Condition or Disease Intervention/Treatment Phase
  • Other: Intervention to Help Orient Men to Excel (IN-HOME)
  • Other: AARP's English "Care at Home" resource webpage
N/A

Detailed Description

The investigators used a randomized, two-group, pretest/posttest design to test the efficacy of the IN-HOME prototype and explore the following research question: To what extent did exposure to the IN-HOME prototype relate to positive changes in CHWs' knowledge, skills, and perceived self-efficacy to conduct outreach to African American and Latino male caregivers of older adults?

The community-focused and community-based approach of the intervention included an evaluation that required strategies to address gender preferences for resources and providing care and cultural awareness to understand the communities of focus. The evaluation recognized additional barriers such as racial/ethnic group historical experiences and racism that effects the groups health outcomes and health care interactions. To ensure that the approach was culturally appropriate and the materials were culturally relevant, the investigators worked with caregiver and health disparities researchers and CHW practitioners to create an advisory committee of experts that provided input into the development of the intervention to empower CHWs to conduct outreach to African American and Latino male caregivers. The PI, with input from the advisory committee, developed necessary research materials, including the recruitment protocols, evaluation instrumentation, and human subjects consent materials. The PI also outlined the appropriate statistical analysis methods. All procedure documents were reviewed by the KDHRC Institutional Review Board before the evaluation launch.

The investigators recruited participants through evaluation partners who disseminated the study information to CHWs via electronic notifications and flyers. Evaluation partners included sites with CHW-related programs and CHW organizations such as, the Virginia CHW Association, the Dallas-Fort Worth CHW Organization, Connection Health, and the Hispanic Health Initiative Incorporated. The notification provided information about the goal of the study, participant eligibility, and a link to an interest and eligibility form. After a potential participant completed the interest and eligibility form and determined as eligible for the project, they received a link to a consent form that was located on a secure online platform.

CHWs were randomly assigned to the intervention or control group after consent and enrollment in the study. All participants completed an online pretest survey. The intervention group was exposed to IN-HOME and completed an online posttest survey two weeks after completing the IN-HOME modules. The control group participants were not exposed to the IN-HOME program but were asked to review the AARP's English "Care at Home" resource webpage. The control group participants completed a posttest two weeks after completing the pretest. Participant responses to pretest and posttest survey measures were linked using non-personal identifiers.

The investigators downloaded and exported the data from Alchemer into an encrypted Excel file and imported the raw data into STATA. The investigators matched the pretest and posttest responses using the random assigned identifiers and conduct analyses to test for the effect of IN-HOME exposure on changes in CHWs' knowledge, skills, and self-efficacy to conduct outreach to African American and Latino male caregivers. Effectiveness measure for intervention feasibility was statistically significant differences between pretest and posttest for knowledge and self-efficacy measures among the intervention group participants.

Study Design

Study Type:
Interventional
Actual Enrollment :
122 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Testing Preliminary Effectiveness of a CHW Training Program to Support African American and Latino Male Caregivers of Older Adults
Actual Study Start Date :
May 22, 2023
Actual Primary Completion Date :
Aug 15, 2023
Actual Study Completion Date :
Aug 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention to Help Orient Men to Excel (IN-HOME)

Professional development training for CHWs on African American and Latino male caregiver needs

Other: Intervention to Help Orient Men to Excel (IN-HOME)
A multi module online training

Other: Control

AARP's English "Care at Home" resource webpage

Other: AARP's English "Care at Home" resource webpage
Caregiver information from the American Association of Retired Persons

Outcome Measures

Primary Outcome Measures

  1. Knowledge, skills, and self-efficacy [Two weeks]

    Social Cognitive Theory (SCT) based behavior change model using a quantitative survey. Investigators designed questions to assess knowledge and skills (through multiple choice questions) that are anticipated to increase for participants exposed to the intervention. A 10-point confidence rating scale to assess self-efficacy/ confidence in performing key skills related to caregiver outreach are included.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 95 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Must self-identify as working as a community health worker

  • Must be actively employed conducting community-based outreach at an organization (paid or volunteer)

  • Must be 18 years of age or older

  • Must live in the United States

Exclusion Criteria:

Contacts and Locations

Locations

Site City State Country Postal Code
1 KDH Research & Communication Atlanta Georgia United States 30309

Sponsors and Collaborators

  • KDH Research & Communication

Investigators

  • Study Chair: Eric C Twombly, PhD, KDH Research & Communication

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
KDH Research & Communication
ClinicalTrials.gov Identifier:
NCT06049043
Other Study ID Numbers:
  • 2023-02-10
First Posted:
Sep 21, 2023
Last Update Posted:
Sep 21, 2023
Last Verified:
Sep 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by KDH Research & Communication
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 21, 2023