Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
ID07282158

Adaptation of Helping Ovarian Cancer Patients Cope (HOPE) for Clinician Burnout (HOPE-C)

Led by Fred Hutchinson Cancer Center · Updated on 2026-06-05

25

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

F

Fred Hutchinson Cancer Center

Lead Sponsor

A

Andy Hill CARE Fund

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating an adapted version of the Helping Ovarian Cancer Patients Cope (HOPE) intervention called HOPE-C, designed to address burnout among gynecologic oncology clinicians. Burnout in these clinicians can negatively impact mental health, professional performance, patient outcomes, and healthcare systems. The original HOPE intervention promotes hope in ovarian cancer patients through positive narratives; HOPE-C tailors these concepts to clinicians by fostering peer support and helping them reframe challenging experiences. The study involves three main objectives. First, clinicians review HOPE-C materials and provide feedback through interviews and questionnaires to help develop the intervention. Next, in a pilot trial, clinicians attend four weekly HOPE-C sessions, each lasting about 30 to 45 minutes, focusing on changing narratives, managing uncertainty, and finding meaning. Before and after these sessions, clinicians complete questionnaires. Finally, clinicians may participate in interviews after completing HOPE-C to further optimize and evaluate the intervention. Participants will be involved in reviewing materials, attending sessions, and completing questionnaires and interviews. Researchers will assess feasibility by tracking accrual rates, intervention completion, and survey completion. They will also measure acceptability, satisfaction, and delivery of the intervention. Data collection occurs at enrollment, during the four-week intervention, and up to two weeks post-intervention. The trial is sponsored by Fred Hutchinson Cancer Center and includes clinicians working with ovarian cancer patients.

CONDITIONS

Brief Title

Adapted Helping Ovarian Cancer Patients Cope Intervention to Address Burnout for Gynecologic Oncology Clinicians

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years of age or older
  • English speaking
  • Able to provide informed consent
  • Working with patients with ovarian cancer (gynecologic oncologists, medical oncologists, nurses, social workers, and advanced practice providers)
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 screening and enrollment visit (in-person or virtual)

Outpatient Treatment

Duration - 4 weeks

Participants attend weekly HOPE-C behavioral intervention sessions focused on changing their narrative, managing life's uncertainty, and finding meaning.

Weekly visits for 4 weeks, each session lasting approximately 30-45 minutes

Follow-up

Duration - Up to 2 weeks post-intervention

Participants complete questionnaires before and after the intervention and may participate in an interview to provide feedback and optimize the intervention.

1 to 2 visits depending on interview participation

Trial Site Locations

Total: 1 location

1

Fred Hutch/University of Washington Cancer Consortium

Seattle, Washington, United States, 98109

Actively Recruiting

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Research Team

M

Megan J. Shen, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

1

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