Actively Recruiting
Pilot Study Evaluating Preoperative Video and Secure Web Platform to Improve Medical Information and Reduce Anxiety in Thyroid Surgery
Led by University Hospital, Montpellier · Updated on 2025-01-21
220
Participants Needed
1
Research Sites
330 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The study focuses on patients undergoing thyroid surgery and aims to evaluate how additional, personalized medical information provided through a secure internet platform affects patients' anxiety levels before surgery. The platform includes an explanatory video about thyroid surgery and offers continuous access to relevant surgical information. Researchers want to see if this extra access can reduce preoperative anxiety compared to receiving standard medical information alone. Participants will be randomly assigned to one of two groups. The control group will receive the usual medical information related to their thyroid surgery, while the experimental group will receive the same usual information plus personalized, secure access to the online platform for additional educational content. This setup allows comparison of anxiety levels between standard care and enhanced information support. Throughout the study, patients will complete self-questionnaires, including the Amsterdam Preoperative Anxiety and Information Scale (APAIS), before and on the day of surgery to assess anxiety levels. The study monitors patient compliance and collects data related to the impact of information delivery on anxiety. Participation involves signing informed consent and spans from the inclusion visit up to the surgery day, with evaluations conducted shortly before surgery.
CONDITIONS
Official Title
Pilot Study for Thyroid Surgery by Preoperative Video Support and Personalized and Secure Web Platform
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 18 and 75
- Indication for lobo-isthmectomy or total thyroidectomy
- Willingness to complete self-questionnaires
- Affiliated with or beneficiary of a social security scheme
- Provided free, informed, and written consent before participation
You will not qualify if you...
- Difficulty understanding French
- No internet access
- Under legal protection such as guardianship or curatorship
- Participating in another research with an ongoing exclusion period
- Severely impaired physical or psychological health affecting study compliance
- Pregnant or lactating woman
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
CHU Gui de Chauliac
Montpellier, Hérault, France, 34295
Actively Recruiting
Research Team
C
Cesar Cartier, PI
S
Susana Leornard, CRA
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
Frequently Asked Questions
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