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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04013230
Other study ID # 2019-02343
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date August 21, 2019
Est. completion date December 30, 2020

Study information

Verified date July 2019
Source Umeå University
Contact Annelie Thorén, MD
Phone +46 73 678 65 93
Email annelie.thoren@rvn.se
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to assess the efficacy of group sessions and a web-based program for children with obesity age 5-12 years and their parents.

The intervention consist of a doctor's appointment, four group-based education sessions over four weeks, psychical activity on prescription and a 12-week web-based treatment program and will be offered to children aged 5-12 years with obesity (International Obesity Task Force-BMI >30), and their parents.


Description:

Obesity in children and adolescents worldwide has increased from 1 % in 1975 to about 6 % in 2016. Experts have estimated that the world will have more obese children and adolescents than underweight at the year 2022. Preventing and reversing excess weight gain in children is important since obesity often tracks into adulthood with adverse health consequences.

Web-based interventions have been shown to be effective, to have a beneficial treatment outcome and have been proposed to have great potential to reach many children and improve cost effectiveness.

This is a randomized controlled study with cross-over design. The intervention consist of a doctor's appointment, four group-based education sessions over four weeks, psychical activity on prescription and a 12-week web-based treatment program. The control group will have standard care treatment consisting of doctor's appointment and, in some cases, contact with dietician.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date December 30, 2020
Est. primary completion date August 30, 2020
Accepts healthy volunteers No
Gender All
Age group 5 Years to 12 Years
Eligibility Inclusion Criteria:

- Obesity according to International Obesity Task Force (IOTF)

- Be able to speak and write Swedish

- Have internet access in parents` home

Exclusion Criteria:

- Obesity together with other severe disease including neuropsychiatric disorder

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Usual care
Visit doctor and nurse at the clinic.
Web-COP
Usual care plus group sessions and a web-based treatment program for 12 weeks for the child and parents.

Locations

Country Name City State
Sweden Outpatient peadictric clinic in Sollefteå hospital Sollefteå
Sweden Outpatient peadiatric clinic in Sundsvalls hospital Sundsvall
Sweden Umeå university Umeå

Sponsors (2)

Lead Sponsor Collaborator
Umeå University Västernorrland County Council, Sweden

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in BMI-SDS Controll vs intervention At baseline, 2, 4 and 6 months
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