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NCT Number: NCT07228377

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

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.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

MedStar Georgetown Cancer Institute at MedStar Washington Hospital Center

Washington D.C., District of Columbia, 20010, United States

Location status: Recruiting

Location contact

Eloisa Leiva

CONTACT

[email protected]

(202) 877-5468

About this study

Patients living with cancer commonly experience chronic pain, defined as pain lasting at least three months. While cancer pain management has traditionally focused on pharmacologic therapies, particularly opioids, pain experts, clinical guidelines, and patients living with cancer increasingly support the use of non-pharmacologic therapies (including mind-body modalities such as distraction, mindfulness, and cognitive behavioral therapy) to mitigate pain and potentially reduce pain medication needs. Virtual reality (VR), a rapidly evolving technology that immerses the user in pleasant, virtual environments, has been shown to lower different forms of acute and chronic pain syndromes, but has not been developed specifically to improve chronic cancer pain. The long-term goal of the investigators is to develop and disseminate a patient-centered, patient-driven VR intervention that significantly improves the chronic cancer pain experience. Towards this end, they propose a multi-phase project involving active patient stakeholder input and an iterative design process that will achieve the following Specific Aims: Aim 1 - to identify patient perceptions around chronic cancer pain experiences and management strategies; Aim 2 - to develop a highly feasible, acceptable, usable, safe VR prototype enabling patient-directed management of cancer pain; Aim 3 - to conduct a trial to assess prototype feasibility, acceptability, usability, and safety. Completion of this project will lead towards development of a scalable VR intervention to mitigate pain that has potential to dramatically improve quality of life and clinical outcomes in patients living with chronic cancer pain.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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)

Exclusion criteria

  • 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.

Treatment and study plan

virtual reality pain therapy

Behavioral

DISCOVR virtual reality pain therapy

Primary outcomes

  1. Intervention feasibility

    Time frame: From enrollment to end of treatment at 7 days

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

Secondary outcomes

  1. Acceptability

    Time frame: Collected at end of 7 days participation

    Technology Acceptance Model questionnaire

  2. Usability

    Time frame: Collected at end of 7 day participation

    System Usability Scale

Study contacts

Contact information is provided by the study sponsor or research team.

Eloisa Leiva

CONTACT

[email protected]

Hunter Groninger, MD

CONTACT

[email protected]

202-877-7445

Sponsors and collaborators

Lead sponsor

Medstar Health Research Institute

Other

Collaborators

  • National Cancer Institute (NCI)

Registry information

Official study title

Digital Intervention for Symptom Management in Cancer and Opioid Sparing Using Virtual Reality (DISCOVR) - Feasibility, Acceptability, Usability Testing of a Novel Intervention

Acronym: DISCOVR

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Nov 14, 2025
Registry last updated
Dec 24, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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