REducing Anxiety in CHildren Undergoing Procedures

Ambulatory Surgery Clinical Trial

— REACH-UP!  

Official title:

Reducing Anxiety in Children Undergoing Procedures

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03054077
• Other study ID #: HM200008056
• Status: Completed
• Phase: N/A
• First received: January 31, 2017
• Last updated: September 12, 2017
• Start date: March 10, 2017
• Est. completion date: May 19, 2017

Study information

• Verified date: September 2017
• Source: Virginia Commonwealth University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a small pilot, feasibility study designed as a quality improvement project. The purpose is to identify anxiety in children aged 4-12 years who will receive a sedated procedure and to see if the use of an iPad as a focused activity will decrease the level of anxiety through a small randomized control trial in the Children's Perioperative Unit.

Description:

Description: The study is a quality improvement project and designed as a small pilot randomized control trial. Participants will be randomly assigned to either Group 1 (no intervention) or Group 2 (iPad intervention) via a number generator.

Children randomized to Group 1 receive the standard of care with observation and scoring of the mYPAS-SF occurring at three time points (T1 pre-operative holding area-patient room which is private, T2 induction of anesthesia, T3 awakening from sedation post procedure).

Children randomized to Group 2 will be observed at the same time points (T1, T2, T3) but will additionally interact with an iPad that has a selection of 3 games downloaded (3 games for children ages 4-7 and 3 games for children ages 8-12). The iPad is introduced in between T1 and T2 and then resumed at T3 until discharge from the clinical unit.

Process: Following IRB approval, the steps of the study are:

1. . Subjects meeting inclusion criteria (age, first sedated procedure, English speaking) will be identified through daily review of scheduled patient lists by study team members. (CPU Nurse Champions, PI).

2. . Potential subjects will be approached in a private area when they arrive for the procedure to make sure they meet the eligibility criteria. Information concerning the study will be presented by the CPU Nurse Champion, PI or Research Assistant.

3. . If the family is interested in participating in the study, further explanation and consent and assent (as appropriate) will be obtained by the PI or the Research Assistant from the parent and the child.

4. . A demographic questionnaire will be completed following project consenting and enrollment for both groups.

5. . The mYPAS-SF (screening tool that requires a 30 second observation at three distinct time points) will be completed for both groups.

6. . The iPad will be given to participants randomized to Group 2 T1- Child observed in the private holding room area (observation occurs after getting settled in the private room prior to the procedure)

T2-Child observed prior to the induction of anesthesia (observation occurs just prior to the administration of anesthesia).

T3-Child observed upon return to private holding area and awakening from anesthesia (observation occurs when child awakens from the anesthesia).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 24
• Est. completion date: May 19, 2017
• Est. primary completion date: May 19, 2017
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 4 Years to 12 Years

Eligibility

Inclusion Criteria:

• Children admitted for a sedated procedure

• Must be first sedated procedure

• English speaking

• ages 4-12

Exclusion Criteria:

• Non English speaking

• Children younger than 4 and older than 12 years

• Children with developmental disabilities

Related Conditions & MeSH terms

• Ambulatory Surgery

Intervention

Other:
• iPad with downloaded games
iPad with downloaded games will be given to children randomized to group 2 for use during their time in the peri-operative unit

Locations

Country	Name	City	State
United States	Virginia Commonwealth University Health System	Richmond	Virginia

Sponsors (1)

Lead Sponsor	Collaborator
Virginia Commonwealth University

Country where clinical trial is conducted

United States, 

References & Publications (4)

Banchs RJ, Lerman J. Preoperative anxiety management, emergence delirium, and postoperative behavior. Anesthesiol Clin. 2014 Mar;32(1):1-23. doi: 10.1016/j.anclin.2013.10.011. Review. — View Citation

Jenkins BN, Fortier MA, Kaplan SH, Mayes LC, Kain ZN. Development of a short version of the modified Yale Preoperative Anxiety Scale. Anesth Analg. 2014 Sep;119(3):643-50. doi: 10.1213/ANE.0000000000000350. — View Citation

Kain ZN, Caldwell-Andrews AA, Mayes LC, Weinberg ME, Wang SM, MacLaren JE, Blount RL. Family-centered preparation for surgery improves perioperative outcomes in children: a randomized controlled trial. Anesthesiology. 2007 Jan;106(1):65-74. — View Citation

Kain ZN, Mayes LC, Cicchetti DV, Bagnall AL, Finley JD, Hofstadter MB. The Yale Preoperative Anxiety Scale: how does it compare with a "gold standard"? Anesth Analg. 1997 Oct;85(4):783-8. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in Anxiety Scores With the Addition of the iPad Intervention-Comparing Group 1 to Group 2	The Modified Yale Preoperative Anxiety Scale- Short form (mYPAS-SF) Ratings produce 4 mYPAS scores (1 for each time point); Areas scored: Activity (1,2,3, or 4) Vocalizations (1,2,3,4,5,or 6) Emotional Expressivity (1,2,3, or 4) State of Apparent arousal (1,2,3, or 4) Scoring: Each score is calculated by dividing each item rating by the highest possible rating (i.e., 6 for the "vocalizations" item and 4 for all other items), adding all the produced values, dividing by 5, and multiplying by 100.; This calculation produces a score ranging from 23.33 to 100, with higher values indicating higher anxiety.; Comparison of scores between Group 1 and Group 2 to see if changes in anxiety scores occurred with the addition of the iPad.; All data will be gathered with review at the close of the study which is anticipated to occur in 5/20/2017.	Immediately following enrollment, immediately before anesthesia, and post-op assessed up to 10 minutes