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NCT00939380 · ClinicalTrials.gov registry record · NA
Facilitating Parent Adaptation to Pediatric Transplant: The P-SCIP Trial
A NA study, sponsored by Rutgers, The State University of New Jersey.
- Completed
- Registry status
- NA
- Development phase
- 212
- Enrollment target
NCT00939380: Completed NA study, sponsored by Rutgers, The State University of New Jersey.
NCT00939380 is a NA study that has completed, run by Rutgers, The State University of New Jersey. The registered enrollment target is 212 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (85% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00939380, a NA study, has completed, sponsored by Rutgers, The State University of New Jersey.
- COMPLETED
- Registry status
- NA
- Development phase
- 212 participants
- Enrollment target
Study Summary
The investigators have developed a parent social-cognitive processing intervention (P-SCIP) to help decrease distress among parent caregivers of children undergoing hematopoietic stem cell transplant (HSCT). The investigators will evaluate the efficacy of P-SCIP in reducing short- and long-term distress and parenting stress among 300 parents of children undergoing HSCT. P-SCIP will be delivered during the child's inpatient HSCT hospitalization and is specifically designed to improve parent social (e.g., sharing concerns) and cognitive (e.g., acceptance) processing of the transplant experience. The intervention includes five in-person sessions that are accompanied by an interactive CD-ROM. The CD-ROM complements the materials in the in-person sessions and provides parents with the opportunity to enhance and deepen their cognitive and social processing of the HSCT experience. The intervention will be tested against best-practices psychosocial care (BPC) available in four enriched pediatric HSCT settings across the United States. P-SCIP will be provided to both Spanish- and English-speaking parents. Participants will complete measures of psychological distress, well-being, and social and cognitive processing at the time of HSCT, two, six and twelve months after HSCT. Research questions will address the effects of P-SCIP versus BPC on parent psychological adaptation and social and cognitive processing, as well as evaluate parent personal resources as well as child medical course variables that contribute to intervention response. The investigators will also examine barriers to participation in the intervention by comparing barriers to participation among parents who refuse participation in the trial and parents who accept.
Interventions
- BEHAVIORAL Behavioral intervention sessions
- OTHER CD-ROM
- OTHER DVD and pamphlet
- OTHER Respite care
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 212 participants |
| Start Date | 2010-05 |
| Est. Completion | 2015-05 |
| Phase | NA |
What the finished NCT00939380 record still lists
NCT00939380 is an interventional study that assigns participants to a tested intervention. The registered 212 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (85% lower).
The record links to 0 conditions, and to 4 interventions - of which Behavioral intervention sessions is the first listed.
NCT00939380 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00939380 about?
NCT00939380 is a clinical study titled "Facilitating Parent Adaptation to Pediatric Transplant: The P-SCIP Trial". The investigators have developed a parent social-cognitive processing intervention (P-SCIP) to help decrease distress among parent caregivers of children undergoing hematopoietic stem cell transplant (HSCT). The investigators will evaluate the efficacy of P-SCIP in reducing short- and long-term dist...
What is the current status of trial NCT00939380?
This trial is currently completed. It is a NA study. The enrollment target is 212 participants. The study started on 2010-05. Estimated completion is 2015-05.
What interventions are being tested in trial NCT00939380?
The interventions under investigation include: Behavioral intervention sessions (BEHAVIORAL), CD-ROM (OTHER), DVD and pamphlet (OTHER), Respite care (OTHER).
Who is sponsoring clinical trial NCT00939380?
This trial is sponsored by Rutgers, The State University of New Jersey, which has 413 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00939380's enrollment target sits among peer trials
212 489th of 2000 higher than 1,511 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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