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Study identifier: NCT06291610 Synced from ClinicalTrials.gov · July 29, 2026
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Feasibility Testing a Decision-support Intervention for Clinical Trials

Condition: Head and Neck Neoplasms  ·  Sponsor: University of Aarhus

PhaseNA
Planned participants60
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Anne Kristensen, MSc  ·  +4530315605  ·  annkrs@rm.dk

Cai Grau, Professor  ·  cai.grau@rm.dk

Always discuss trial participation with your own doctor first.

Locations (1)

Aarhus University HospitalAarhus, DenmarkRecruiting

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Source record: clinicaltrials.gov/study/NCT06291610