Using Hypnosis to Help Children Undergoing a Difficult Medical Procedure
Sponsor
Stanford University (Other)
Overall Status
Completed
CT.gov ID
NCT00226850
Collaborator
(none)
2
Study Details
Study Description
Brief Summary
This study examined whether a hypnosis intervention, compared to standard care, could help reduce distress and pain for children undergoing an invasive medical procedure.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 3 |
Study Design
Study Type:
Interventional
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Outcome Measures
Primary Outcome Measures
Eligibility Criteria
Criteria
Ages Eligible for Study:
5 Years
to 18 Years
Sexes Eligible for Study:
All
Inclusion Criteria:
- The child: (1) was scheduled for an upcoming VCUG ; (2) must have undergone at least one previous VCUG; (3) was at least 4 years of age at the time of the previous VCUG; (4) experienced distress during the previous VCUG; and (5) both child and participating parent were English speaking.
Exclusion Criteria:
- Not meeting any of the above criteria.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Department of Psychiatry & Behavioral Sciences, Stanford University School of Medicine | Stanford | California | United States | 94305-5718 |
| 2 | Lucile Packard Children's Hospital | Stanford | California | United States | 94305 |
Sponsors and Collaborators
- Stanford University
Investigators
- Study Director: Lisa D. Butler, Ph.D., Stanford University
- Principal Investigator: David Spiegel, M.D., Stanford University
- Principal Investigator: Linda D Shortliffe, M.D., Stanford University
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
,
,
ClinicalTrials.gov Identifier:
NCT00226850
Other Study ID Numbers:
- 1HUK610
First Posted:
Sep 27, 2005
Last Update Posted:
Sep 27, 2005
Last Verified:
Sep 1, 2005