Quality of Life in Pediatric Transplant Patients

Sponsor
Medical College of Wisconsin (Other)
Overall Status
Terminated
CT.gov ID
NCT00678002
Collaborator
(none)
57
1
145
0.4

Study Details

Study Description

Brief Summary

The goal of this study is to compare parent and child perceptions of wellness and vulnerability in children who have undergone solid organ transplant. It is hypothesized that there will be significant differences between parent and child perceptions.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    There are numerous studies that report on the quality of life in solid organ transplant recipients. However, very few studies target quality of life parameters for these children and their families across all solid organ transplantation. Furthermore, no literature directly addresses a comparison of perceptions and wellness, impact on family, and vulnerability in a comparative format by these distinct, but definitely related populations.

    The goal of this study is to compare parent and child perceptions of wellness and vulnerability in children who have undergone solid organ transplant. It is hypothesized that there will be significant differences between parent and child perceptions. Outcomes will be measured by using five different instruments:

    1. Pediatric Quality of Life Inventory (PedsQL)

    2. PedsQL Family Impact Module

    3. PedsQL Family Information Form

    4. Functional Status II-R

    5. Child Vulnerability Scale (CVS)

    Patients will be enrolled at the time of transplant listing, or after transplant. Patients and families will complete the survey once every 6 months while the patient is active on the respective transplant waiting list. After transplant, the patients and families will be asked to complete the survey once every 6 months for the first two years and annually thereafter.

    This study may provide us with an improved understanding of parent and child perceptions in wellness, impact on family, and vulnerability within each transplant group. The results may also indicate trend differences between these three populations. These differences may help to provide insight into family perspectives allowing for greater anticipatory guidance and targeted interventions.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    57 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Quality of Life and Vulnerability in Pediatric Solid Organ Transplant Recipients
    Study Start Date :
    Oct 1, 2008
    Actual Primary Completion Date :
    Nov 1, 2020
    Actual Study Completion Date :
    Nov 1, 2020

    Arms and Interventions

    Arm Intervention/Treatment
    QOL###

    All child subjects in this cohort will be listed for or already have received a solid organ transplant (kidney, heart, or liver).

    Outcome Measures

    Primary Outcome Measures

    1. Pediatric Quality of Life Inventory [every 6 months]

    Secondary Outcome Measures

    1. Peds QL Family Impact Module [every 6 months]

    2. Peds QL Family Information Form [every 6 months]

    3. Functional Status II-R [every 6 months]

    4. Child Vulnerability Scale [every 6 months]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A to 21 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • between newborn and 21 years old

    • parent/child pairs of patients listed for or who have received a liver transplant, kidney transplant, or heart transplant

    Exclusion Criteria:
    • unwilling or unable to participate

    • not in one of the above transplant groups

    • non-English speaking

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Children's Hospital of Wisconsin Milwaukee Wisconsin United States 53226

    Sponsors and Collaborators

    • Medical College of Wisconsin

    Investigators

    • Principal Investigator: Stacee Lerret, CPNP, Medical College of Wisconsin
    • Principal Investigator: Gail Stendahl, CPNP, Children's Hospital and Health System Foundation, Wisconsin

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Stacee Lerret, Advanced Practice Nurse, Medical College of Wisconsin
    ClinicalTrials.gov Identifier:
    NCT00678002
    Other Study ID Numbers:
    • CHW 08/157
    • GC173
    First Posted:
    May 15, 2008
    Last Update Posted:
    Nov 30, 2020
    Last Verified:
    Nov 1, 2020
    Keywords provided by Stacee Lerret, Advanced Practice Nurse, Medical College of Wisconsin

    Study Results

    No Results Posted as of Nov 30, 2020