Digital Intervention for Symptom Management in Cancer and Opioid Sparing Using Virtual Reality (DISCOVR) Study

ConditionCancer
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorMedstar Health Research Institute

About this trial

Patients living with cancer commonly have chronic pain due to the disease or to cancer treatments. Virtual reality, a new technology that immerses the user in pleasant, diverting, and exciting virtual environments, may lower chronic cancer pain to improve quality of life and complement need for pain medications like opioids. The investigators aim to learn from patients about the experience of cancer pain, develop a virtual reality prototype specific to cancer pain management, and test the feasibility and acceptability of this technology to improve the cancer pain experience.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

age ≥18 years old

living with active cancer diagnosis (any solid tumor type)

report chronic cancer pain (≥3 months) with baseline severity moderate-severe (i.e., self-report pain score (SRPS) ≥4/10, where 0=no pain, 10=worst pain)

prescribed chronic opioid therapies (may be long-acting formulations, short-acting formulations, or both)

Disqualifiers

history of intractable nausea/vomiting, motion sickness, seizures/epilepsy, and/or cranial structure abnormalities preventing VR headset use

moderate-severe pain of non-cancer etiology (e.g., chronic lumbago)

enrolled in another pain study

unable to complete surveys in English or Spanish.

Trial design

Design model

Single group

Treatments tested in this trial

  • virtual reality pain therapy

    Behavioral

    DISCOVR virtual reality pain therapy

Treatment groups

25 Participants
are divided into 1 treatment group
Group A: Virtual reality pain therapyExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Intervention feasibility

\>70% of participants completing the prescribed use of VR headset daily (≥10 minutes) for one week

Time frame
From enrollment to end of treatment at 7 days

Secondary outcomes

1

Acceptability

Technology Acceptance Model questionnaire

Time frame
Collected at end of 7 days participation
2

Usability

System Usability Scale

Time frame
Collected at end of 7 day participation

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Medstar Health Research Institute

Lead sponsor

National Cancer Institute (NCI)

Collaborator