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NCT05737602

Promoting Stress Management and Resilience Among Individuals With Von Hippel- Lindau Disease

ENROLLING BY INVITATION NA Last updated 29 May 2025
What this trial tests

NA trial testing 3RP-VHL in Von Hippel-Lindau Disease in 40 participants. Enrolling by invitation.

Timeline
30 July 2024
Primary endpoint
1 May 2026
1 July 2026

Quick facts

Lead sponsorMassachusetts General Hospital
PhaseNA
StatusENROLLING BY INVITATION
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposesupportive care
Enrollment40
Start date30 July 2024
Primary completion1 May 2026
Estimated completion1 July 2026
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Massachusetts General Hospital

Who can join

18 and older, any sex, with Von Hippel-Lindau Disease or Genetic Disorder. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The Relaxation Response Resiliency Program (3RP) has shown efficacy in improving coping and resilience across diverse populations; however, little is known about how it helps individuals manage the challenges of living with a chronic illness. This study proposes to pilot test an adapted version of the 3RP among patients living with VHL.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other recruiting trials for Von Hippel-Lindau Disease

Currently open trials in the same condition.

Other Massachusetts General Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05737602.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing