Ask Questions About Clinical Trials
ASQ-CT
1 other identifier
interventional
293
1 country
8
Brief Summary
The overall goal of this study is to assess the implementation of the Ask Questions about Clinical Trials (ASQ-CT) brochure, a patient-focused communication tool previously demonstrated to improve patient-provider communication about clinical trials. Participants will be given the ASQ-CT brochure at Time 1 (baseline) and participants will complete a questionnaire at three timepoints, baseline (Time 1), Pre-Research Visit (Time 2), and Post-Research Visit (Time 3).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Dec 2026
8 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 15, 2025
CompletedFirst Posted
Study publicly available on registry
January 15, 2026
CompletedStudy Start
First participant enrolled
December 30, 2026
ExpectedPrimary Completion
Last participant's last visit for primary outcome
December 30, 2027
Study Completion
Last participant's last visit for all outcomes
April 5, 2028
August 6, 2026
June 1, 2026
1 year
December 15, 2025
August 4, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Effectiveness - Self-Efficacy in managing patient-provider interactions - Quantitative Scale
Improvement of self-efficacy in managing patient-providers interactions between baseline (Time 1) and pre-clinic visit (Time 2). Measured using scale of 1-5 where a higher score is equal to a better outcome
From Baseline (Time 1) to end of Pre-Clinic Visit (Time 2)
Secondary Outcomes (10)
Reach - Number and Proportion
At start of Participation
Effectiveness - Self-Efficacy in managing patient-provider interactions - Quantitative Scale
From Pre-Clinic (Time 2) to end of Post-Clinic Visit (Time 3) up to 3 months.
Effectiveness - Knowledge - Quantitative Scale
From Baseline (Time 1) to end of Pre-Clinic Visit (Time 2)
Effectiveness - Knowledge - Quantitative Scale
From Pre-Clinic Visit (Time 2) to end of Post-Clinic Visit (Time 3) up to 3 months
Effectiveness - Trust - Quantitative Scale
From Baseline (Time 1) to end of Pre-Clinic Visit (Time 2)
- +5 more secondary outcomes
Study Arms (1)
Ask Questions about Clinical Trials (ASQ-CT) Brochure
EXPERIMENTALAsk Questions about Clinical Trials (ASQ-CT), a clinical trial communication intervention brochure
Interventions
Communication intervention called a question prompt list
Eligibility Criteria
You may qualify if:
- Age \> or equal to 18 years
- Appointment to see a provider at a Karmanos Cancer Institute-McLaren or a medical encounter at McLaren Center for Research and Innovation (MCRI) site for medical/systemic treatment
- Potentially eligible for a clinical trial
- Speak and read English well enough to be able to understand consent documents and complete surveys
You may not qualify if:
- Not able to complete study documents on their own physically or cognitively
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (8)
Karmanos Cancer Institute at McLaren Bay Region
Bay City, Michigan, 48706, United States
Karmanos Cancer Institute at McLaren Clarkston
Clarkston, Michigan, 48346, United States
Karmanos Cancer Institute at McLaren Greater Lansing
Lansing, Michigan, 48910, United States
Karmanos Cancer Institute at McLaren Lapeer
Lapeer, Michigan, 48446, United States
Karmanos Cancer Institute at McLaren Macomb
Mount Clemens, Michigan, 48043, United States
Karmanos Cancer Institute at McLaren Central Michigan, Morey Cancer Center
Mount Pleasant, Michigan, 48858, United States
Karmanos Cancer Institute at McLaren Northern Michigan
Petoskey, Michigan, 49770, United States
Karmanos Cancer Institute at McLaren Port Huron
Port Huron, Michigan, 48060, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Lauren M Hamel, PhD, MBA
Wayne State University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
December 15, 2025
First Posted
January 15, 2026
Study Start (Estimated)
December 30, 2026
Primary Completion (Estimated)
December 30, 2027
Study Completion (Estimated)
April 5, 2028
Last Updated
August 6, 2026
Record last verified: 2026-06