ClinicalTrials.Veeva

Menu

An Evaluation of a Web-based System for Optimization of Behavioral Childhood Obesity Treatment

Karolinska Institute logo

Karolinska Institute

Status

Completed

Conditions

Childhood Obesity

Treatments

Behavioral: CLOSS
Behavioral: Usual care

Study type

Interventional

Funder types

Other

Identifiers

NCT03380598
CLOSS100

Details and patient eligibility

About

This study evaluates the families' and health care professional's experience from using a web based support system including mobile applications for self-monitoring weight and physical activity. Changes in BMI standard deviation score are compared between usual care (control) and usual care with complementary web-based support system (intervention).

Full description

In this study children with obesity were randomized to either usual care according to regular routine (control group) or to usual care plus a web-based support system (intervention group). The system is based on a smartphone application connected to a scale and an activity measuring wrist-band. Data is automatically transferred from the accessories to the smartphone, where data is presented graphically. The data is transferred to the clinic for support. The system is developed for communication between the clinic and family. The randomization was done at the start of individual treatment and lasted for 6 months. Investigators studied the families and health care professional's experience of using the web-based support system as well as changes in BMI standard deviation score in the control and intervention group.

Enrollment

28 patients

Sex

All

Ages

5 to 12 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Obesity according to International Obesity Task Force (IOTF)
  • Swedish speaking parents
  • Parents able to use a smart phone
  • No pharmacological treatment that could intervene the obesity treatment

Exclusion criteria

  • Diagnosed with or undergoing assessment of neuropsychiatric disorder
  • Structured obesity treatment the past 6 months
  • Hypothalamic obesity

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

28 participants in 2 patient groups

Usual care
Active Comparator group
Description:
Usual care according to regular treatment routines at the clinic during 6 months.
Treatment:
Behavioral: Usual care
CLOSS
Active Comparator group
Description:
Usual care plus using a web based support system for self-monitoring weight at physical activity.
Treatment:
Behavioral: CLOSS

Trial contacts and locations

3

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems