NCT07228377

Brief Summary

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.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
25

participants targeted

Target at below P25 for not_applicable cancer

Timeline
2mo left

Started Dec 2025

Shorter than P25 for not_applicable cancer

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress72%
Dec 2025Aug 2026

First Submitted

Initial submission to the registry

November 13, 2025

Completed
1 day until next milestone

First Posted

Study publicly available on registry

November 14, 2025

Completed
17 days until next milestone

Study Start

First participant enrolled

December 1, 2025

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 31, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 31, 2026

Last Updated

December 24, 2025

Status Verified

November 1, 2025

Enrollment Period

9 months

First QC Date

November 13, 2025

Last Update Submit

December 22, 2025

Conditions

Keywords

cancer painchronic painopioidvirtual realitytechnology

Outcome Measures

Primary Outcomes (1)

  • Intervention feasibility

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

    From enrollment to end of treatment at 7 days

Secondary Outcomes (2)

  • Acceptability

    Collected at end of 7 days participation

  • Usability

    Collected at end of 7 day participation

Study Arms (1)

Virtual reality pain therapy

EXPERIMENTAL
Behavioral: virtual reality pain therapy

Interventions

DISCOVR virtual reality pain therapy

Virtual reality pain therapy

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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)

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

MedStar Georgetown Cancer Institute at MedStar Washington Hospital Center

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

RECRUITING

MeSH Terms

Conditions

NeoplasmsCancer PainChronic Pain

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Hunter Groninger, MD

    Medstar Health Research Institute

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Hunter Groninger, MD

CONTACT

Eloisa Leiva

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

November 13, 2025

First Posted

November 14, 2025

Study Start

December 1, 2025

Primary Completion (Estimated)

August 31, 2026

Study Completion (Estimated)

August 31, 2026

Last Updated

December 24, 2025

Record last verified: 2025-11

Locations