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Evaluation of a Digital Childhood Obesity Treatment

One Year Evaluation of a Web-based System for Optimization of Behavioural Childhood Obesity Treatment

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04323215
Enrollment
156
Registered
2020-03-26
Start date
2018-09-01
Completion date
2020-05-01
Last updated
2020-11-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Childhood Obesity, Treatment Adherence

Keywords

Mobile Health, Support System, Behavioral treatment, Self-Monitoring

Brief summary

This study aims to evaluate if a web-based digital support system aiming to replacing or complement standardized pediatric behavioural obesity treatment. The hypothesis is that a digital system of communication between the family and the clinic can generate improved treatment results (change in BMI SDS) and reduce the number of missed visits.

Detailed description

Childhood obesity treatment is time consuming for both the health care system, and for the involved families. There is an association between the intensity and the outcome of treatment. In this study all children who start treatment for childhood obesity will use a digital support system as a complement to behavioral treatment. The digital support system includes daily weighing on scales that do not show any digits, linked to a mobile app where weight development is shown as a moving average in the form of BMI standard deviation score (SDS). The app also provides an individual target curve visualizing the expected weight journey. Weight in growing children is complex to interpret why BMI SDS is used. Objective data from scale are automatically transferred to the database and the clinic and the family have direct contact with the clinic via the app. The evaluation will be carried out when approximately 120 children have had the opportunity to be treated with the support system for one year. The results will be compared with a matched control group from the BORIS childhood obesity treatment register.

Interventions

DEVICESupport system

A support system named Provement will be used to provide behavioral treatment.

Sponsors

Karolinska Institutet
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
3 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* Obesity according to International Obesity Task Force (IOTF)

Exclusion criteria

* No

Design outcomes

Primary

MeasureTime frameDescription
Change in degree of obesityFrom start of treatment to one year follow-upMeasured by BMI standard deviation score. Support system users vs control

Secondary

MeasureTime frameDescription
The use of the support system - weighingsFrom start of treatment to one year follow-upNumber of weighings/week
The use of the support system - text messagesFrom start of treatment to one year follow-upNumber text messages/week
Number of physical visitsFrom start of treatment to one year follow-upVisits to the clinic. Support system users vs control
Number of cancelation of physical visitsFrom start of treatment to one year follow-upVisits to the clinic. Support system users vs control
Number of patients not showing up to physical visitFrom start of treatment to one year follow-upVisits to the clinic. Support system users vs control

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 12, 2026