Parents of Pediatric Solid Organ Transplant Recipients: Transition to Home and Chronic Illness Care
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Purpose
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 |
|---|
|
Transplant |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Official Title: | Parents of Pediatric Solid Organ Transplant Recipients: Transition to Home and Chronic Illness Care |
- 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 [ Time Frame: 2 years ] [ Designated as safety issue: No ]
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.
- Post transplant outcomes [ Time Frame: 2 years ] [ Designated as safety issue: No ]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.
| Enrollment: | 51 |
| Study Start Date: | July 2010 |
| Study Completion Date: | January 2012 |
| Primary Completion Date: | January 2012 (Final data collection date for primary outcome measure) |
| Groups/Cohorts |
|---|
|
Pediatric Solid Organ Transplant
Parents of pediatric solid organ transplant recipients
|
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.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Parents of pediatric solid organ transplant recipients (heart, kidney, liver or lung)
Inclusion Criteria:
- the parent's child has undergone a heart, kidney, liver, lung or multivisceral transplant and is being discharged home from the hospital
- the parent is English speaking (tools being used have been validated for English participants only)
- the parent is 18 years of age or older
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
- the child has already experienced the discharge to home transition after a previous transplant.
Contacts and Locations| United States, Illinois | |
| Children's Memorial Hospital | |
| Chicago, Illinois, United States, 60614 | |
| United States, Missouri | |
| St. Louis Children's Hospital | |
| St. Louis, Missouri, United States, 63110 | |
| United States, Nebraska | |
| Children's Hospital and Medical Center of Nebraska | |
| Omaha, Nebraska, United States, 68114 | |
| United States, North Carolina | |
| Levine Children's Hospital | |
| Charlotte, North Carolina, United States, 28203 | |
| United States, Wisconsin | |
| Children's Hospital of Wisconsin | |
| Milwaukee, Wisconsin, United States, 53146 | |
| Principal Investigator: | Stacee Lerret, PhD(c), RN | Medical College of Wisconsin/Children's Hospital of Wisconsin |
More Information
No publications provided
| Responsible Party: | Stacee Lerret, Assistant Professor, Medical College of Wisconsin |
| ClinicalTrials.gov Identifier: | NCT01389804 History of Changes |
| Other Study ID Numbers: | CHW10/115,GC 1127 |
| Study First Received: | September 3, 2010 |
| Last Updated: | April 19, 2012 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Medical College of Wisconsin:
|
transplant, pediatric |
Additional relevant MeSH terms:
|
Chronic Disease Disease Attributes Pathologic Processes |
ClinicalTrials.gov processed this record on May 16, 2013