Parents of Pediatric Solid Organ Transplant Recipients: Transition to Home and Chronic Illness Care

Sponsor
Medical College of Wisconsin (Other)
Overall Status
Completed
CT.gov ID
NCT01389804
Collaborator
Children's National Research Institute (Other)
51
5
18
10.2
0.6

Study Details

Study Description

Brief Summary

The overall long term objective of this research is to improve health care utilization and quality of life of pediatric solid organ transplant recipients and family. Understanding the process of transition to a chronic medical condition during the acute (3 weeks after transplant) and long term (3 and 6 months) will significantly guide the development of clinical interventions aimed at maximizing adherence and family psychosocial adjustment.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Parents of children that have received a heart, kidney, liver or lung transplant will be invited to participate in this protocol.

    Involvement in this study entails completion of questionnaires at 4 separate time points. Parents will first complete questionnaires regarding discharge teaching, care coordination and readiness for hospital discharge on the day of discharge from the hospital. Parents will subsequently complete questionnaires at 3 weeks, 3 months and 6 months after discharge. The post discharge questionnaires assess coping, family management, adherence and utilization of healthcare resources.

    Currently, no research has been conducted related to readiness for hospital discharge of a parent as the primary caregiver for a child with solid organ transplant or the sequential relationships between hospitalization care and the trajectory of post-discharge outcomes. This research will fill the gap in knowledge needed for care of solid organ transplant children and parents.

    The ability to identify factors in the first year after transplant that are predictive of decreased coping and non-adherence affords an opportunity to develop nursing and health interventions that have significant implications for care decisions, as well as disease activity and health care costs.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    51 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Parents of Pediatric Solid Organ Transplant Recipients: Transition to Home and Chronic Illness Care
    Study Start Date :
    Jul 1, 2010
    Actual Primary Completion Date :
    Jan 1, 2012
    Actual Study Completion Date :
    Jan 1, 2012

    Arms and Interventions

    Arm Intervention/Treatment
    Pediatric Solid Organ Transplant

    Parents of pediatric solid organ transplant recipients

    Outcome Measures

    Primary Outcome Measures

    1. Determine if discharge preparation has an effect on parent readiness for hospital discharge and if readiness for hospital discharge effects post-discharge outcomes following hospital discharge in parents of solid organ transplant recipients [2 years]

      Determine if discharge preparation (discharge teaching and care coordination) for parents of solid organ transplant children has an effect on: (1) short term discharge transition outcomes and transition to home-based care (measured at 3 weeks post-discharge) and,(2) longer term chronic care outcomes at 3 and 6 months post-discharge.

    Secondary Outcome Measures

    1. Post transplant outcomes [2 years]

      Determine outcomes (parent coping, adherence, family management, and utilization of healthcare services) and the relationship between these outcomes, throughout the transition to chronic care management for families of solid organ transplant recipients at 3 weeks, 3 months and 6 months post-discharge.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. the parent's child has undergone a heart, kidney, liver, lung or multivisceral transplant and is being discharged home from the hospital

    2. the parent is English speaking (tools being used have been validated for English participants only)

    3. the parent is 18 years of age or older

    Exclusion Criteria:
    1. presence of significant communication or cognitive impairment on the part of the parent that would preclude completion of questionnaires based on self-report

    2. the child has already experienced the discharge to home transition after a previous transplant.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Children's Memorial Hospital Chicago Illinois United States 60614
    2 St. Louis Children's Hospital St. Louis Missouri United States 63110
    3 Children's Hospital and Medical Center of Nebraska Omaha Nebraska United States 68114
    4 Levine Children's Hospital Charlotte North Carolina United States 28203
    5 Children's Hospital of Wisconsin Milwaukee Wisconsin United States 53146

    Sponsors and Collaborators

    • Medical College of Wisconsin
    • Children's National Research Institute

    Investigators

    • Principal Investigator: Stacee Lerret, PhD(c), RN, Medical College of Wisconsin/Children's Hospital of Wisconsin

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Stacee Lerret, Assistant Professor, Medical College of Wisconsin
    ClinicalTrials.gov Identifier:
    NCT01389804
    Other Study ID Numbers:
    • CHW10/115,GC 1127
    First Posted:
    Jul 8, 2011
    Last Update Posted:
    Apr 23, 2012
    Last Verified:
    Apr 1, 2012
    Keywords provided by Stacee Lerret, Assistant Professor, Medical College of Wisconsin
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 23, 2012