Discharge to Home and Chronic Illness Care Pilot

NCT ID: NCT02165423

Last Updated: 2019-03-07

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-06-30

Study Completion Date

2018-10-31

Brief Summary

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The purpose of this study is to address a gap in knowledge needed for care of children with solid organ transplantation (SOT) and their parents by combining mHealth technology with an individualized family centered self-management intervention (referred to as myFAMI). This study is critical to the increased understanding of hospital to home transition and family management at home with the potential to transform the way clinicians approach the care of complex chronic illness children and families.

Detailed Description

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Conditions

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Solid Organ Transplant

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

SINGLE

Participants

Study Groups

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Control

Ten parents will be randomized to the control group defined as 'usual care' and ten to the intervention group, stratified by type of transplant.

Group Type EXPERIMENTAL

myFAMI iPad application

Intervention Type BEHAVIORAL

Intervention

Ten parents will be randomized to the control group defined as 'usual care' and ten to the intervention group, stratified by type of transplant.

Group Type EXPERIMENTAL

myFAMI iPad application

Intervention Type BEHAVIORAL

Interventions

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myFAMI iPad application

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* parent's child has undergone a heart, kidney, or liver transplant and is being discharged home from the hospital
* the parent is English speaking (to date the tools being used have been validated for English participants only)
* parent is 18 years of age or older
* patient is 17 years of age and younger.

Exclusion Criteria

* presence of significant communication or cognitive impairment on the part of the parent that would preclude completion of questionnaires based on self-report
* parent and child has experienced the discharge to home transition from a previous transplant.
Minimum Eligible Age

18 Years

Maximum Eligible Age

90 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Children's National Research Institute

OTHER

Sponsor Role collaborator

Medical College of Wisconsin

OTHER

Sponsor Role lead

Responsible Party

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Stacee Lerret

Assistant Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Stacee Lerret, PhD

Role: PRINCIPAL_INVESTIGATOR

Medical College of Wisconsin

Locations

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Children's Hospital of Wisconsin

Milwaukee, Wisconsin, United States

Site Status

Countries

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United States

Other Identifiers

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CHW 14/66

Identifier Type: -

Identifier Source: org_study_id

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