Using Hypnosis to Help Children Undergoing a Difficult Medical Procedure
This study has been completed.
Sponsor:
Stanford University
Information provided by:
Stanford University
ClinicalTrials.gov Identifier:
NCT00226850
First received: September 12, 2005
Last updated: September 23, 2005
Last verified: September 2005
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Purpose
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 | Intervention | Phase |
|---|---|---|
|
Voiding Cystourethrogram (VCUG) |
Behavioral: hypnosis |
Phase 3 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Parallel Assignment Masking: Open Label |
Further study details as provided by Stanford University:
Eligibility| Ages Eligible for Study: | 5 Years to 18 Years |
| Genders Eligible for Study: | Both |
Criteria
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
Please refer to this study by its ClinicalTrials.gov identifier: NCT00226850
Locations
| United States, California | |
| Department of Psychiatry & Behavioral Sciences, Stanford University School of Medicine | |
| Stanford, California, United States, 94305-5718 | |
| 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 |
More Information
Publications:
| ClinicalTrials.gov Identifier: | NCT00226850 History of Changes |
| Other Study ID Numbers: | 1HUK610 |
| Study First Received: | September 12, 2005 |
| Last Updated: | September 23, 2005 |
| Health Authority: | United States: Institutional Review Board |
ClinicalTrials.gov processed this record on May 23, 2013