ASk Questions in GYnecologic Oncology (ASQ-GYO)

Not Applicable

Recruiting

• Conditions: Gestational Trophoblastic Disease; Cervical Cancer; Vaginal Cancer; Ovarian Cancer; Vulvar Cancer; Endometrial Cancer
• Interventions: Behavioral: Administration of the ASk Questions in GYnecologic Oncology (ASQ-GYO) Question Prompt List

• Registration Number: NCT06339827
• Lead Sponsor: Ira Winer

Brief Summary

The goal of this clinical trial is to determine the effectiveness of the ASk Questions in GYnecologic Oncology question prompt list (ASQ-GYO QPL) at improving patient self-efficacy, distress, physician trust, and knowledge compared to usual care during new patient gynecologic oncology visits. Also to determine the acceptability of the ASQ-GYO QPL with new gynecologic oncology patients.

Detailed Description

* Potential participants who are scheduled for a new patient appointment will be contacted via phone or email to determine if they are interested in participating.

* If a participant is interested, they will choose their preferred method of consenting (phone, email, or in person) and if they would like to complete the pre-visit survey now or at a later time prior to their appointment

* If consented, all participants will be provided with the pre-survey questionnaire. If eligible, participants will then be randomized to usual care or the intervention (ASk Questions in GYnecologic Oncology question prompt list (ASQ-GYO QPL)

* If randomized to receive the ASQ-QYO QPL, they will be emailed this document and given a paper copy of the ASQ-GYO QPL in the waiting room prior to their visit to ensure they have received the intervention.

* Directly after the participant's visit, all participants will be asked to complete the post-visit survey on a tablet in the clinic waiting room, or via a secure link in an email within 1 week of the appointment.

* After completion of the post-visit survey and within one month of their visit, participants who were not randomized to receive the ASQ-GYO QPL will be sent the ASQ-GYO QPL via email so that they may also have access to this resource.

Study Timeline

• Study First Submitted: 2024-03-21
• Study First Submitted QC: 2024-03-27
• Study First Posted: 2024-04-01
• Study Start: 2024-04-04
• Status Verified: 2024-05
• Last Update Submitted: 2024-05-15
• Last Update Posted: 2024-05-16
• Primary Completion: 2026-05
• Study Completion: 2027-05

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 70

Inclusion Criteria

• 18 years of age
• Understands spoken and written English
• Able to consent to study participation
• Biopsy confirmed gynecologic cancer diagnosis (ovarian, endometrial, cervical, vulvar, or vaginal cancer or Gestational Trophoblastic Disease) OR have imaging and/or laboratory findings highly concerning for a cancer diagnosis and have not seen a Gynecologic Oncologist

Exclusion Criteria

• pathologic diagnosis of dysplasia only (cervical, vulvar, or endometrial)
• History and/or imaging/laboratory findings more indicative of a non-cancer diagnosis
• Previous treatment discussion with a Gynecologic Oncologist

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Administration of the ASk Questions in GYnecologic Oncology (ASQ-GYO) Question Prompt List	Administration of the ASk Questions in GYnecologic Oncology (ASQ-GYO) Question Prompt List	Participants are provided with a question prompt list

Primary Outcome Measures

Name	Time	Method
Change in pre- and post-visit self-efficacy scores and compared by trial group	All participants will complete the PEPPI instrument twice: within 2 weeks of their first visit and again within 1 week after the visit.	The Perceived Efficacy in Patient-Provider Interactions (PEPPI) instrument is a validated, 20-item, 5-point Likert scale tool designed to measure patient's self-efficacy in obtaining medical information and attention to their medical concerns from physicians.

Secondary Outcome Measures

Name	Time	Method
Change in pre- and post-visit National Comprehensive Cancer Network (NCCN) Distress Thermometer scores compared by trial group	All participants, Twice: within 2 weeks of the first visit and again within 1 week after the visit	The NCCN Distress Thermometer is a one-question, 11-point Likert scale for patient-reported distress in the past week including today
Knowledge Screen	All participants will complete a post-visit knowledge screen once within 1 week after their visit	The Knowledge Screen is a 10-item, 5-point Likert scale, investigator-developed set of questions designed to elicit understanding of the contents of the Question Prompt List with higher scores indicating more understanding.
Change in pre- and post-visit Trust in a Physician scores compared by trial group	All participants, Twice: within 2 weeks of the first visit and again within 1 week after the visit	The Trust in a Physician score is a validated, 5-point Likert scale with higher scores indicating more trust. The metric addresses generic physician trust prior to the visit, and trust in the specific physician the patient saw during their visit for after the visit
Patient perceptions of the Question Prompt List	The patients in the intervention group will complete this within 1 week after their visit.	This is a 15-item investigator-developed set of questions with 7 items utilizing a 5-point Likert scale and 8 items utilizing binary yes/no questions designed to elicit the acceptability of the Question Prompt List among the patients in the intervention group.

Trial Locations

Locations (1)

Barbara Ann Karmanos Cancer Institute; 🇺🇸 Detroit, Michigan, United States