A Phase II Randomized Controlled Trial to Determine the Efficacy of an auGmented reAlity gaMe in pediatrIc caNcer Patients Who Are Opioid Naïve Undergoing Surgery to Reduce Postoperative Opioid Use (GAMING-ON Study)

M.D. Anderson Cancer Center

Status and phase: Enrolling; Phase 2

Conditions: Pediatric ALL; Cancer

Treatments: Other: Augmented Reality; Other: IPAD

Study type: Interventional

Funder types: Other; NIH

Identifiers

NCT05466994

NCI-2022-05979 (Other Identifier)

2022-0336

Details and patient eligibility

About

To learn if playing an augmented reality game called SpellBound can reduce pain and the need for opioids in young patients scheduled for surgery.

Full description

Primary Objective:

•To assess the efficacy of SpellBound's AR-enabled scavenger hunt to reduce the rate of 90-day opioid use in pediatric cancer patients undergoing surgery compared to a control non-AR game in a randomized controlled trial.

Secondary Objectives:

To assess the effect of AR versus non-AR control technology in pediatric oncology patients, including:

• Inpatient opioid use
• Average daily inpatient pain score
• Number of opioid requests during the hospital stay
• Inpatient PedsQL (quality of life) questionnaire score
• Ambulation/"out of bed" movement
• Number days to discharge-ready status
• Patient experience assessed by satisfaction scores on a questionnaire designed by MD Anderson Cancer Center Child Life team.
• Outpatient opioid consumption reported at 30, 60, and 90 days
• Outpatient pain scores reported at 30, 60, and 90 days
• Outpatient PedsQL scores reported at 30, 60, and 90 days
• Potential adverse events related to the use of AR (i.e., falls).

Enrollment: 34 estimated patients

Sex: All

Ages: 5 to 15 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Ages 5-15

2. English and Spanish-speaking parents/legal guardians and patients

3. Undergoing major surgery for cancer requiring postoperative hospitalization is defined as ≥2 hours of duration of surgery and requiring postoperative hospital admission of at least one night

4. Expected to be prescribed postoperative inpatient opioids

5. Have never taken opioids or have had no daily opioid use within the last 30 days before surgery

6. Sufficient cognitive capacity to comprehend and interact with the game. This is defined as the ability to utilize mobile technology (use iPad with or without assistance) and activate and respond to AR experiences within the app as determined by the clinician.

7. Both the child and a legal guardian are willing and able to provide informed consent.

   • The range from 5-to 15 is based on a recent pilot RCT in which the PI found that older adolescents (>15 years of age) were disinterested in the interactive game.

Exclusion criteria

1. Patients with any daily opioid use within 30 days before surgery.
2. History of documented peripheral neuropathy secondary to cancer treatment
3. Inability to demonstrate an understanding of the game from English instructions
4. Any additional concerns based on the study physicians' assessments

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Single Group Assignment

Masking: None (Open label)

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34 participants in 2 patient groups

Group 1(Spellbound)

Other group

Description:

Participants will play the game using the iPad's standard camera, which will show you your hospital room and the decals as they appear in the real world.

Treatment:

Other: IPAD

Group 2 (Spellbound)

Other group

Description:

Participants will play the game using augmented reality

Treatment:

Other: Augmented Reality