Von Hippel-Lindau Disease Clinical Trial

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

Summary

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.

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Full Description

The 3RP has not been carried out with VHL patients. As such, the investigators are looking to see if an adapted program, tailored to the needs of patients with VHL, is feasible, acceptable, and helpful in improving coping among individuals living with VHL.

This study is a two phase trial. Phase I is descriptive. It is comprised of conducting interviews with patients and caregivers to understand the challenges of living with VHL and patient's programatic needs. This information will be used to tailor the program for patients living with VHL. Phase II is a single-arm feasibility trial that will examine if the adapted program is feasible, acceptable, and helps promote stress management among VHL patients. To these means, we will test the adapted 3RP (3RP-VHL) in up to 40 patients living with VHL. Participants will complete surveys at baseline and post 3RP-VHL program completion. This record will reflect the trial component (Phase II) only, as feasibility and acceptability outcomes will be collected for this phase.

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Eligibility Criteria

Inclusion Criteria:

Ages 18+
Confirmed diagnosis of VHL

Exclusion Criteria:

Is medically, psychiatrically, or otherwise unable to participate (as determined by a physician or study PI).
Unwilling or unable to participate in study sessions delivered via Partners Telehealth videoconferencing.
Participated in Phase 1 qualitative interview.

Study is for people with:

Von Hippel-Lindau Disease

Estimated Enrollment:

40

Study ID:

NCT05737602

Recruitment Status:

Not yet recruiting

Sponsor:

Massachusetts General Hospital

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There is 1 Location for this study

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Massachusetts General Hospital Cancer Center
Boston Massachusetts, 02215, United States More Info
Giselle Perez, PhD
Contact
617-724-0765
[email protected]

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Study is for people with:

Von Hippel-Lindau Disease

Estimated Enrollment:

40

Study ID:

NCT05737602

Recruitment Status:

Not yet recruiting

Sponsor:


Massachusetts General Hospital

How clear is this clinincal trial information?

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