Optimizing a Personalized Health Approach for Virtually Treating High-risk Caregivers During COVID-19 and Beyond

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goal of this clinical trial is to learn which types of telehealth-based treatments best fit the needs of caregivers of people with rare neurogenetic conditions. The main questions it plans to answer are: * Which telehealth support programs best meet the needs of rare disorder caregivers? * How can individuals be matched to support programs that are right for them? What aspects of an individual (e.g., demographics, mental health symptoms, family characteristics, lifestyle) predict whether treatment will be a good fit? * Does peer-to-peer coaching help improve patients' experiences during telehealth treatment? Participants will be asked to complete a 12-week treatment program, which may include self-guided resources, individual therapies, group therapies, and/or peer-to-peer coaching. Before, during, and after treatment, participants will complete questionnaires to help researchers understand their experiences, symptoms, and impressions of their support program. Questionnaires will include both standard forms (administered up to 5 times throughout the study) and brief snapshot surveys that participants complete on their smartphones up to 3 times per day. Some participants will be assigned to a waitlist control, which means that they will provide data while they are not yet completing a support program. These participants will be assigned to a support program in the next treatment phase.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 70
Healthy Volunteers: t
View:

• Caregiver and legal guardian of child age 2-35 with neurogenetic condition

• Child's syndrome must (1) have an established genetic cause, (2) affect the brain, resulting in moderate to severe intellectual disability in the majority of patients

• Reside in US

• Fluent in English (spoken and written)

• Seeking support for caregiver mental health/well-being and/or caregiving needs

Locations
United States
Indiana
Purdue University
RECRUITING
West Lafayette
Contact Information
Primary
Bridgette L Kelleher, PhD
bkelleher@purdue.edu
18438100238
Time Frame
Start Date: 2023-06-28
Estimated Completion Date: 2025-12-29
Participants
Target number of participants: 800
Treatments
Experimental: No Algorithm + Participation Enhancement Intervention
Participants are randomly assigned to support program without use of a personalized health algorithm AND receive the participation enhancement intervention.
Experimental: No Algorithm + No Participation Enhancement Intervention
Participants are randomly assigned to support program without use of a personalized health algorithm AND do not receive the participation enhancement intervention.
Experimental: Algorithm 1 + Participation Enhancement Intervention
Participants are assigned to support programs using Algorithm 1 AND receive the participation enhancement intervention.
Experimental: Algorithm 1 + No Participation Enhancement Intervention
Participants are assigned to support programs using Algorithm 1 AND do not receive the participation enhancement intervention.
Experimental: Algorithm 2 + Participation Enhancement Intervention
Participants are assigned to support programs using Algorithm 2 AND receive the participation enhancement intervention.
Experimental: Algorithm 2 + No Participation Enhancement Intervention
Participants are assigned to support programs using Algorithm 2 AND do not receive the participation enhancement intervention.
Experimental: Algorithm 3 + Participation Enhancement Intervention
Participants are assigned to support programs using Algorithm 3 AND receive the participation enhancement intervention.
Experimental: Algorithm 3 + No Participation Enhancement Intervention
Participants are assigned to support programs using Algorithm 3 AND do not receive the participation enhancement intervention.
No_intervention: Waitlist Control
Participants are enrolled in the waitlist control condition, which includes identical data collection procedures to participants enrolled in support programs. Waitlist controls are offered the opportunity to enroll in future cycles.
Related Therapeutic Areas
Sponsors
Collaborators: Indiana University, University of Canterbury, Georgia State University, University of Missouri-Columbia, University of Oregon, University of Virginia
Leads: Purdue University

This content was sourced from clinicaltrials.gov