Evaluating a Telemedicine-based Intensive Treatment Program for Children and Adolescents With Obesity
- Conditions
- Obesity, Childhood
- Interventions
- Behavioral: Intensive lifestyle consultations
- Registration Number
- NCT05700409
- Lead Sponsor
- Sheba Medical Center
- Brief Summary
The study objective is to evaluate whether a novel telemedicine-based intensive treatment program for children with obesity is superior to standard on-site care. This will be a randomized, non-blinded (due to the nature of the intervention) study, where 100 children and adolescents aged 10-18 years with obesity will be divided in a 1:1 ratio to either telemedicine or on-site treatments for 6 months.
The telemedicine arm will include 30, mostly video, consultations for each participant: 3 physician appointments, 7 exercise consultations by our exercise physiologist, 10 dietary consultations by our pediatric dietitian, and 10 psychologist consultations to assist with goal setting and overall well-being. Three visits will be conducted in-office, for physician assessment, smartphone technical assistance and physical measurements (baseline, at 3 months and at the end of the 6-month period). Participants randomized to the telemedicine arm will have a step-counting rewarding app installed on their smartphone by our staff.
The in-office arm will have 6 monthly visits during the study period, with two consultations performed in each visit - one by the physician or exercise physiologist, and one by our pediatric dietitian.
The main outcome of the study is BMI standard deviation (z-score) changes, which will be evaluated after 3 and 6 months of treatment during physical office visits in both study arms.
Secondary outcomes will be:
* Body-fat percent changes, assessed by bioimpedance analysis in physical clinic visits.
* Daily step counts, measured by smartphone data/ wearable activity tracker, if available.
* Weight-related quality of life
* Retention and visit cancellation rates.
* Satisfaction of both parent and child from their allocated treatment.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 100
- Obesity, defined as a BMI at or above 2 standard deviations SDs according to the WHO growth reference
- Owning a smartphone, needed for video conversations, step counting and the gamification app
- Parent consent and child's assent to participate in the program
- Significant physical or mental barriers to physical activity and/or to dietary changes (such as autistic spectrum disorder that precludes dietary changes or sufficient exercise, as assessed by the PI)
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Telemedicine Intensive lifestyle consultations The telemedicine arm will include 30, mostly video, consultations for each participant: 3 physician appointments, 7 exercise consultations by our exercise physiologist, 10 dietary consultations by our pediatric dietitian, and 10 psychologist consultations to assist with goal setting and overall well-being. Three visits will be conducted in-office, for physician assessment, smartphone technical assistance and physical measurements (baseline, at 3 months and at the end of the 6-month period). Participants randomized to the telemedicine arm will have a step-counting rewarding app installed on their smartphone by our staff. On-site Intensive lifestyle consultations The on-site arm will have 6 monthly visits during the study period, with two consultations performed in each visit - one by the physician or exercise physiologist, and one by our pediatric dietitian.
- Primary Outcome Measures
Name Time Method Weight status From baseline to 6 months BMI z-score change
- Secondary Outcome Measures
Name Time Method Daily step counts At 6 months Body-fat percent changes From baseline to 6 months Weight-related quality of life 6 months Scores on the Impact of Weight on Quality of Life (IWQOL)-Kids questionnaire OR "Sizing me up" questionnaire
Visit cancellation rates 6 months Retention in program 6 months Duration of participation in the program
Satisfaction of allocated treatment 6 months Generic PROM questionnaire used in our hopital
Trial Locations
- Locations (1)
Sheba Medical Center
🇮🇱Ramat Gan, State/Province, Israel