Obesity, Adolescent Clinical Trial
— PM2Official title:
PathMate2: The Impact of Health Information System Services on the Effects of Therapy in Overweight Teenagers
Verified date | January 2020 |
Source | Ostschweizer Kinderspital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Randomised controlled trial in overweight adolescents using a health App.
Status | Completed |
Enrollment | 40 |
Est. completion date | December 31, 2018 |
Est. primary completion date | December 31, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 11 Years to 18 Years |
Eligibility |
Inclusion Criteria: - obesity, BMI > P. 97 (Jenni et al., 2011) or overweight, BMI >P.90, plus risk factors or co-morbidity - ability and parent's permission to use pre-configured study smartphones handed out to the children - readiness to use the personal smartphone number and to spend the sum allocated exclusively for the study SMS during the 6 months of intervention Exclusion Criteria: - major somatic or psychiatric disease without adequate treatment, - weight-relevant medication (antiepileptic drugs, methylphenhydate and similar medication), - inability or lack of parent's or caregivers' permission to use a study smartphone with a mobile phone contract, - lack of informed consent from children and parents and - undue consumption of the amount allocated for study SMS for non-study purposes, - overuse of smartphone e.g. without night beak for at least 8 hours. |
Country | Name | City | State |
---|---|---|---|
Switzerland | Ostschweizer Kinderspital | St. Gallen | Saint Gallen |
Lead Sponsor | Collaborator |
---|---|
Ostschweizer Kinderspital |
Switzerland,
Haug S, Kowatsch T, Castro RP, Filler A, Schaub MP. Efficacy of a web- and text messaging-based intervention to reduce problem drinking in young people: study protocol of a cluster-randomised controlled trial. BMC Public Health. 2014 Aug 7;14:809. doi: 10.1186/1471-2458-14-809. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Body Mass Index | Main outcome parameter is Body Mass Index, as BMI-SDS adjusted for gender & age. Group size of 4*20 was based on an expected decrease by -0.23±0.02 (SDS, Mean±SD) after 1 year, from initially 2.88±0.7. | 12 months | |
Secondary | fitness / physical capability | Eurofit-test | 12 months | |
Secondary | fitness / physical activity | accelerometry | 12 months | |
Secondary | stress reduction, biological measure | Cortisol levels in blood | 12 months | |
Secondary | stress and arousal | Self-Assessment Manikin (SAM) Scale | 12 months | |
Secondary | reduction of chronic stress | Trierer Stress Inventar questionnaire (TICS) | 12 months | |
Secondary | stress and arousal, biophysical measure | skin conductance (Nexus 10) | 12 months | |
Secondary | well-being | KIDSCREEN | 12 months | |
Secondary | waist circumference | Waist-to-Height-ratio or SDS according to Fredricks 2005 | 12 months |
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