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NCT00261261 · ClinicalTrials.gov registry record · NA
Family-Centered Behavioral Preparation for Surgery
A NA study, sponsored by Yale University.
- Completed
- Registry status
- NA
- Development phase
- 400
- Enrollment target
NCT00261261 is a NA study that has completed, run by Yale University. The registered enrollment target is 400 participants.
The verdict
NCT00261261, a NA study, has completed, sponsored by Yale University.
- COMPLETED
- Registry status
- NA
- Development phase
- 400 participants
- Enrollment target
Study Summary
Children experience significant anxiety and distress during the preoperative period. Currently available interventions are ineffective and/or associated with significant disadvantages. These interventions exclusively target the child and do not attempt to reduce parental anxiety. Based on an integration of the literature in both the anesthesia and psychological milieus, we developed ADVANCE, a behaviorally oriented anxiety reduction program for children undergoing surgery that targets the family as a whole.
Interventions
- DRUG Midazolam
- BEHAVIORAL ADVANCE
- PROCEDURE Parental presence
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 400 participants |
| Start Date | 2001-01 |
| Est. Completion | 2004-12 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00261261
The ClinicalTrials.gov registry entry for NCT00261261 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 400 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Yale University, which has 1,492 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 3 interventions - of which Midazolam is the first listed.
NCT00261261 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00261261 about?
NCT00261261 is a clinical study titled "Family-Centered Behavioral Preparation for Surgery". Children experience significant anxiety and distress during the preoperative period. Currently available interventions are ineffective and/or associated with significant disadvantages. These interventions exclusively target the child and do not attempt to reduce parental anxiety. Based on an integra...
What is the current status of trial NCT00261261?
This trial is currently completed. It is a NA study. The enrollment target is 400 participants. The study started on 2001-01. Estimated completion is 2004-12.
What interventions are being tested in trial NCT00261261?
The interventions under investigation include: Midazolam (DRUG), ADVANCE (BEHAVIORAL), Parental presence (PROCEDURE).
Who is sponsoring clinical trial NCT00261261?
This trial is sponsored by Yale University, which has 1,492 total clinical trials registered on ClinicalTrials.gov.
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