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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03835390
Other study ID # IRB-P00030717
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 22, 2019
Est. completion date October 1, 2019

Study information

Verified date September 2020
Source Boston Children's Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a pilot study aiming to examine preliminary effectiveness of a preparation program which includes simulation (SIMDiscovery) in reducing anxiety and increasing feelings of preparedness among parents and their children who will undergo spinal fusion surgery. SIMDiscovery is an experiential learning preparation program which aims to educate children and families about different medical procedures through simulation play.


Recruitment information / eligibility

Status Completed
Enrollment 22
Est. completion date October 1, 2019
Est. primary completion date September 9, 2019
Accepts healthy volunteers No
Gender All
Age group 10 Years to 18 Years
Eligibility Inclusion Criteria:

- Children and adolescents with adolescent idiopathic scoliosis and their parent(s)

- Spinal fusion surgery scheduled

- Developmental Age range (10+; no upper age range)

- Males and females of all races and ethnicities

- English-speaking families (although English need not be their primary language)

- Both patient and caregiver (when patient is under 18 years of age) are able to attend SIMDiscovery program

Exclusion Criteria:

- - Other significant chronic medical conditions (e.g., spina bifida, muscular dystrophy)

- Anterior surgical access

- ICU stay expected post-op

- Cognitive functioning level below 10yo

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
SIMDiscovery
The SIMDiscovery program consists of nine stations that were designed to mirror the different stages of the perioperative process. The stations mirror the different stages of the surgical process and provide patients and their families with education regarding what they can anticipate during each aspect of the intervention.

Locations

Country Name City State
United States Boston Children's Hospital Boston Massachusetts

Sponsors (1)

Lead Sponsor Collaborator
Boston Children's Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change from Parent's and Adolescent's Baseline Anxiety at 1 month using the State/Trait Anxiety Inventory Parent and adolescent anxiety will be measured at baseline utilizing the State/Trait Anxiety Inventory (STAI) (Spielberger et al., 1983). The STAI consists of 40 items total-20 items assessing trait anxiety (general proneness to anxious behavior) and 20 items assessing state anxiety (a current emotional state). All items are scored using a four-point scale (e.g., ranging from "Almost Never" to "Almost Always"). Scores can range from 20 to 80 with higher scores indicating greater anxiety. This measure has been validated for use with individuals ages 15 and above (Julian, 2011). If a patient is 15 years of age or above, they will complete the STAI, rather than the STAIC (see below). Baseline, 1 month
Primary Change from Child's Baseline Anxiety at 1 month using the State/Trait Anxiety Inventory for Children Child anxiety will be assessed utilizing the State/Trait Anxiety Inventory for Children (STAIC) (Spielberger & Edwards, 1973). Similar to the STAI, the STAIC consists of 20 items assessing state anxiety and 20 items assessing trait anxiety. Items are scored using a four-point scale and higher scores indicate greater anxiety. The STAIC has been validated for use with children up to age 15 years (Spielberger & Edwards, 1973). Baseline, 1 month
Primary Change from Parent's Baseline Feelings of Preparedness at 1 month using Caregiver Preparedness Scale Parent preparedness will be measured using the Caregiver Preparedness Scale (CPS) (Archbold, et al., 1990). This scale has been validated for use with adult caregivers (Petruzzo et al., 2017; Pucciarelli et al., 2014). The CPS includes eight items assessing caregiver preparedness to care for a patient's physical and emotional needs, setting up services, coping with the stress of caregiving, making caregiving activities pleasant for the caregiver and patient, responding and managing emergencies, obtaining assistance from the health care system, and overall preparedness. Each item is rated from 0 (not at all prepared) to 4 (Very well prepared). Items are summed for a total score that ranges from 0 to 32, with higher scores indicating feeling better prepared for the caregiving role. Baseline, 1 month
Primary Change from Child's Baseline Feelings of Preparedness at 1 month using a modified Caregiver Preparedness Scale In order to examine themes similar to parent preparedness but from the patient's perspective, we will administer a measure similar to the CPS (above) for children and adolescent patients. This measure has not been validated; rather, based on the validity of the CPS used to assess parent preparedness, we modified the measure to assess patients' perception of their ability to care for or advocate for themselves regarding their physical and emotional needs prior to the surgery. (Archbold, et al., 1990). All patients will complete this measure. This measure consists of six questions and similar to the CPS, each item is rated from 0 (not at all prepared) to 4 (Very well prepared). Items are summed for a total score that ranges from 0 to 24, with higher scores indicating more feelings of preparedness for the surgery. Baseline, 1 month
Secondary Knowledge of Perioperative Procedures measured by Spinal Fusion Knowledge Assessment Facts that patients learn through the preoperative appointment and the SIMDiscovery program measured by the Spine Fusion Knowledge Assessment developed by our team Baseline, 1 month
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