Actively Recruiting
VICO-trial: Video Consultations in the Follow-up of Children With Functional Abdominal Pain Disorders
Led by Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) · Updated on 2024-10-30
208
Participants Needed
1
Research Sites
78 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this non-inferiority randomized controlled multi-center trial is to investigate the use of video consultations in the follow-up care of children aged 4 - 18 years old with functional abdominal pain disorders (FAPDs). Video consultations will be compared to face-to-face consultations. Clinical outcomes and patients' and parents' healthcare experience will be compared between both groups. Primary outcome is adequate relief after 12 weeks: the hypothesis is that video consultations are not inferior to face-to-face consultations regarding clinical outcomes and that adequate relief will be the same for both groups. Participants and/or parents will be asked to complete a diary for 1 week and a questionnaire after every consultation: at baseline, after 6 weeks and after 12 weeks.
CONDITIONS
Official Title
VICO-trial: Video Consultations in the Follow-up of Children With Functional Abdominal Pain Disorders
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Children aged 4 years to 17 years
- Diagnosed with one of the four types of Functional Abdominal Pain Disorders (functional dyspepsia, irritable bowel syndrome, abdominal migraine, functional abdominal pain not otherwise specified) according to Rome IV criteria
- Able to participate in video consultations
You will not qualify if you...
- No follow-up consultation is needed
- Follow-up consultations must be conducted face to face
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Amsterdam UMC, location AMC
Amsterdam, Netherlands
Actively Recruiting
Research Team
M
M.M. Tabbers, Dr. Phd.
CONTACT
A
A. de Geus, Bsc.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
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