- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05336591
COVID-19, Obesity and Lifestyle in Children - Role of Professionals (COLC-Pro)
August 9, 2022 updated by: Maastricht University Medical Center
In this study it is researched how preventive and curative healthcare for children with overweight and obesity was conducted during the Covid-19 pandemic, which barriers were noticed by professionals, and how new methods (such as e-health and telemonitorning) for coaching, communication and healthcare were used and experienced.
Study Overview
Status
Recruiting
Intervention / Treatment
Study Type
Observational
Enrollment (Anticipated)
385
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Anita CE Vreugdenhil, Prof
- Phone Number: 0031433875284
- Email: a.vreugdenhil@mumc.nl
Study Contact Backup
- Name: Lisanne Arayess, MD
- Email: lisanne.arayess@mumc.nl
Study Locations
-
-
Limburg
-
Maastricht, Limburg, Netherlands, 6229 ER
- Recruiting
- Maastricht University Medical Center
-
Contact:
- A.C.E. Vreugdenh
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Professionals working with children with overweight and/or obesity.
Description
Inclusion Criteria:
- Worked during the Covid-19 pandemic
- Works with children with overweight and / or obesity
- Works in The Netherlands
Exclusion Criteria:
- No knowledge of the Dutch language.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Other
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Medical doctor
|
All participants worked during the Covid-19 pandemic in the preventive or curative healthcare for children with overweight and obesity.
We will ask all professionals about their experiences during and after the pandemic.
|
Nurses (Pediatric department and youth healthcare)
|
All participants worked during the Covid-19 pandemic in the preventive or curative healthcare for children with overweight and obesity.
We will ask all professionals about their experiences during and after the pandemic.
|
Other professionals in treatment (e.g. dieticians, physiotherapists)
|
All participants worked during the Covid-19 pandemic in the preventive or curative healthcare for children with overweight and obesity.
We will ask all professionals about their experiences during and after the pandemic.
|
Other (such as policy makers)
|
All participants worked during the Covid-19 pandemic in the preventive or curative healthcare for children with overweight and obesity.
We will ask all professionals about their experiences during and after the pandemic.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Views and experiences of health care professionals working with children with overweight and obesity during the COVID-19 pandemic
Time Frame: 2 years after the start of the Covid-19 pandemic
|
Views and experiences of health care professionals working with children with overweight and obesity during the COVID-19 pandemic measured with a questionnaire using open-end and closed-end (likert-scale) questions.
|
2 years after the start of the Covid-19 pandemic
|
User experience
Time Frame: 2 years after the start of the Covid-19 pandemic
|
User experience of professionals using ehealth options in healthcare for children with overweight or obesity, measured with a questionnaire using closed end and open end questions.
|
2 years after the start of the Covid-19 pandemic
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Experiences
Time Frame: 2 years after the start of the Covid-19 pandemic
|
In case more in-depth data is needed after the inital questionnaire, semi-structured interviews will be conducted to experiences of health care professionals during the Covid-19 pandemic.
|
2 years after the start of the Covid-19 pandemic
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Anita CE Vreugdenhil, Prof, MUMC+, Maastricht University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
April 21, 2022
Primary Completion (Anticipated)
August 1, 2022
Study Completion (Anticipated)
April 20, 2023
Study Registration Dates
First Submitted
April 19, 2022
First Submitted That Met QC Criteria
April 19, 2022
First Posted (Actual)
April 20, 2022
Study Record Updates
Last Update Posted (Actual)
August 12, 2022
Last Update Submitted That Met QC Criteria
August 9, 2022
Last Verified
August 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Coronavirus Infections
- Coronaviridae Infections
- Nidovirales Infections
- RNA Virus Infections
- Virus Diseases
- Infections
- Respiratory Tract Infections
- Respiratory Tract Diseases
- Pneumonia, Viral
- Pneumonia
- Lung Diseases
- Overnutrition
- Nutrition Disorders
- Body Weight
- COVID-19
- Obesity
- Pediatric Obesity
- Overweight
Other Study ID Numbers
- 2020-1634
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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