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DVD-Based Training Program in Self-Hypnosis for Children

DVD-Based Training Program in Self-Hypnosis for Children: A Randomized Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01483105
Acronym
VCUG
Enrollment
12
Registered
2011-12-01
Start date
2011-10-31
Completion date
2012-07-06
Last updated
2022-05-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Vesicoureteral Reflux

Keywords

VCUG, Child, Hypnosis, Relaxation, Voiding cystourethrography

Brief summary

The proposed study is designed to utilize a self-hypnosis DVD home-training program for parents to use with their children to teach self-hypnosis techniques for inducing relaxation and hypnotic analgesia. These relaxation techniques can be employed to manage anticipatory anxiety, distress, and pain during an invasive medical procedure, for example, voiding cystourethrography (VCUG). The study will examine the efficacy of this intervention for children undergoing VCUG procedures.

Detailed description

Pediatric care professionals and parents seek safe ways to make invasive medical procedures less stressful and traumatic for children. However, for unpleasant procedures that require child cooperation, this task becomes difficult. Home-training in self-hypnotic relaxation may provide an inexpensive, yet systematic method for improving the overall medical care of children undergoing invasive medical procedures. The proposed study is designed to utilize a self-hypnosis DVD home-training program for parents to use with their children to teach self-hypnosis techniques for inducing relaxation and hypnotic analgesia. The study will examine the efficacy of this intervention for children undergoing urethral catheterization for VCUG procedures. Parents will be instructed to watch the DVD and practice the self-hypnosis exercises every day for a week with their child prior to the upcoming procedure. Parents are encouraged to practice self-hypnosis during their child's VCUG procedure. Both parents and children will be asked to complete a series of questionnaires before and following the procedure.

Interventions

BEHAVIORALDVD Self-Hypnosis Training Program

The DVD training program contains instructional materials developed by an experienced psychiatrist and psychologist at the Department of Psychiatry at Stanford University School of Medicine. Parents will be instructed to review these materials, watch the DVD, and practice the self-hypnosis exercises every day for a week with their child prior to the upcoming procedure. Parents are encouraged to practice self-hypnosis during their child's VCUG procedure.

Sponsors

Lucile Packard Children's Hospital
CollaboratorOTHER
Stanford University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
4 Years to 12 Years
Healthy volunteers
No

Inclusion criteria

* Child and participating parent have assented (child) or consented (parent) to participate * Both child and parent are English-speaking * Child has undergone at least one previous VCUG * Child was at least 4 years of age at the time of the most recent VCUG * Parent reports child experienced some difficulty (e.g., at least some crying, pain, or fear) during that earlier procedure.

Exclusion criteria

* Child and participating parent have not assented (child) or consented (parent) to participate * Either child or parent are not English-speaking * Child has not undergone at least one previous VCUG * Child was under 4 years of age at the time of the most recent VCUG * Parent reports child did not experience difficulty (e.g., at least some crying, pain, or fear) during that earlier procedure.

Design outcomes

Primary

MeasureTime frameDescription
Distress: Child Self-ReportSame day - one week after procedureCrying will be assessed by having the child point to a picture on a continuous visual analog scale of 6 different faces representing increasing levels of distress, ranging from a smiling face to a face crying intensely.
Distress: Parent ReportSame day - one week after procedureParent assessments of child distress (fear, pain, and crying)and overall trauma will be completed on 5-point scales, ranging from not at all to extremely. Parents will also rate of how traumatic the present VCUG procedure was compared with the previous one was completed on a 6-point scale ranging from much less traumatic to much more traumatic.
Distress: Observational RatingsSame day - while the child is undergoing the VCUG procedure. Time can range from minutes - hours of observation.A research associate will rate the child's distress from the time he or she enters the procedure room until the procedure is completed. A modified 8-point version of the Torrance Global Mood Scale will be used.

Secondary

MeasureTime frameDescription
DVD EvaluationSame day - 3 months following procedureThe DVD Evaluation form will ask parents to evaluate the DVD-based training program.
Difficulty of Procedure: Medical Staff RatingsDirectly following procedure - up to 30 minutes following the end of procedure.Immediately after the procedure, the attending radiologist and the technician each will be asked to rate the degree of difficulty of conducting the procedure. Staff will be asked to make the ratings with respect to children of similar ages on a 7-point scale ranging from far easier to far more difficult.
Duration of ProcedureSame day - Time can range from minutes - hours of observation.Time in minutes of the VCUG procedure will be recorded from when the child first enters the room to when the child is told the procedure is over.
Anxiety: Parent Self-ReportDirectly following procedure - up to 30 minutes following the end of procedure.Parents will complete the State-Trait Anxiety Inventory (Spielberger, 1970) immediately following the procedure.
Parent ConfidenceDirectly following procedure - 1 weekParent confidence in helping their child through the VCUG procedure will be assessed immediately following the procedure up to 1 week.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026