NCT06666218

Helping Ovarian Cancer Patients Cope With Their Illness (HOPE)

Helping Ovarian Cancer Patients Cope With Their Disease (HOPE) - Phase 2

• Status: Suspended
• Phase: N/A
• Study type: Interventional
• Enrollment: 60 (estimated)
• Sponsor: Fred Hutchinson Cancer Center · Academic / Other
• Sex: Female
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

This clinical trial compares the effect of the Helping Ovarian Cancer Patients Cope with Their Disease (HOPE) intervention to usual care for the reduction of hopelessness and helplessness in patients with ovarian cancer that has come back after a period of improvement (recurrent). Patients with recurrent ovarian cancer are at high risk for increased death and poor mental health outcomes, including depression and anxiety. Ovarian cancer is the deadliest of all gynecologic cancers, with a survival rate at five years of only 50%. Most patients are diagnosed with advanced disease and have a high chance of recurrent disease that is incurable, even if upfront treatments are effective. Ovarian cancer's advanced diagnosis, high likelihood of recurrence and death, and rigorous treatment including surgery and other cancer therapies create high levels of distress and reduced quality of life (QOL). Patients with recurrent ovarian cancer report high rates of depression and anxiety and poor QOL. Due to the major distress, reduced QOL, and likelihood of death among this population, improving this patient population's QOL is a priority. Using the HOPE intervention may be effective in reducing hopelessness and helplessness in recurrent ovarian cancer patients.

Detailed description

OUTLINE: AIM 1: Patients complete the HOPE intervention workshop virtually or in-person. The workshop consists of 3 sessions, each held once per week and lasting 60 to 90 minutes as well as complete a survey and an interview for HOPE intervention refinement during follow up. AIM 2: Patients are randomized to 1 of 2 groups. GROUP I: Patients complete the HOPE intervention workshop virtually or in-person, with 3 sessions held once per week, each lasting 60 to 90 minutes. GROUP II: Patients receive usual care on study. Patients in both groups complete baselines and follow up assessments 5, 8, and 12 weeks after the randomization event.

Conditions

• Recurrent Ovarian Carcinoma

Interventions

Type	Name	Description
BEHAVIORAL	Behavioral Intervention	Complete the HOPE intervention workshop
OTHER	Electronic Health Record Review	Ancillary studies
OTHER	Interview	Complete an interview
OTHER	Survey Administration	Complete a survey
OTHER	Survey Administration	Ancillary studies

Timeline

• Start date: 2025-02-24
• Primary completion: 2027-01-31
• Completion: 2027-01-31
• First posted: 2024-10-30
• Last updated: 2026-01-14

Locations

1 site across 1 country: United States