Actively Recruiting
Feasibility Testing a Decision-support Intervention for Clinical Trials
Led by University of Aarhus · Updated on 2024-03-04
60
Participants Needed
1
Research Sites
149 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
A decision-support intervention are developed for a Danish nationwide randomised controlled trial (RCT) among patients with laryngeal and pharyngeal cancer referred to curative intended radiotherapy. The primary endpoints in this RCT are levels of dysphagia and xerostomia. The decision-support intervention consists of three components, including (1) a patient decision aid tailored to clinical trial participation and (2) decision coaching consultations carried out by trained healthcare professionals. Finally, (3) a training program in decision coaching will be an integrated part of the intervention. To feasibility test (beta test) the intervention, 60 patient participants will be included, separated into pre- (n=30) and post- (n=30) intervention groups. Pre-intervention to complete the survey based on current clinical practice. Post-intervention to complete the survey following engagement in the decision support intervention. A total of 12 physicians will be recruited and trained in decision coaching. To assess the acceptability of the intervention, the physicians will be interviewed. Additionally, they will be asked to audio-record two decision coaching sessions to test the fidelity of the intervention.
CONDITIONS
Official Title
Feasibility Testing a Decision-support Intervention for Clinical Trials
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with cancer of the pharynx or larynx
- Received verbal information regarding DAHANCA 35
- Read the patient information folder from DAHANCA 35
- Above 18 years
- Danish speaking
You will not qualify if you...
- Dyslexia
AI-Screening
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Trial Site Locations
Total: 1 location
1
Aarhus University Hospital
Aarhus, Denmark, 8200
Actively Recruiting
Research Team
A
Anne Kristensen, MSc
CONTACT
C
Cai Grau, Professor
CONTACT
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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