Fact CheckerSign in

NCT06665893Completed

Local Proof of Concept of Evira in Abu Dhabi Study

Evaluating the Efficacy of the Evira Treatment Tool for Childhood Obesity Treatment - a 26- Week Single Arm Interventional Study in Abu Dhabi, United Arab Emirates

Source: ClinicalTrials.gov · Last updated 30 Oct 2024

Brief summary (registry, in English)

Evira is a digital treatment tool developed for treatment of childhood obesity. Through daily weighings at home using a special scale together with a message function in the Evira application, parents and the clinicians can easily follow the child's weight development. The primary aim of this study is to evaluate its efficacy for childhood obesity treatment in Abu Dhabi, with a secondary objective to establish non-inferiority compared to outcomes in a cohort in Stockholm, Sweden.

Status (registry)
Completed
Study type
Interventional
Enrollment
70 (actual)
First submitted
29 Oct 2024
Start date
1 Jun 2023
Primary completion date
30 Jun 2024
Lead sponsor
Sheikh Shakhbout Medical City
Diseases
Obesity
NCT number
NCT06665893

What you commit to

  • Study type: Interventional
  • Participants enrolled: 70
  • From 1 Jun 2023 to the primary completion date, 30 Jun 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Treatment for depression and other psychiatric disorders during the last 6 months before inclusion
  • Eating disorders requiring therapy during the last six months before inclusion or observed at the inclusion screening.

Other illness

  • Endocrine disorders other than well controlled hypothyroidism
  • Metabolic disorders of importance for weight control
  • Hypothalamic or monogenic obesity, e.g. syndromes and Mb Down
  • Severe neuropsychiatric disorders that could affect study compliance

Age

  • Morbid obesity defined as iso-BMI\>40 kg/m2 independently of age

Other

  • Pharmacological treatment of importance for weight control

Who the study is looking for

  • Age \>6.0 and \<16.0 years of age at inclusion
  • Obesity according to International Obesity Task Force (IOTF)
  • Willingness to participate in an obesity treatment proof of concept trial
  • Family ability to communicate e.g. write and read messages in the mobile application
  • Parents having a smart phone and an email address

Age in the registry: 6 years to 16 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Sheikh Shakhbout Medical City
Coordinator of this site? Confirm its status
Abu DhabiUnited Arab EmiratesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.