Eating Disorders Symptoms Clinical Trial
Official title:
Development of Eating Disorders Symptoms Among Children Who Took Part in Family-based Obesity Treatment and Among Their Siblings
Randomized Clinical Trial, the research will be composed of two parts in order to examine the
research question: a combination of controlled randomized retrospective research and
prospective cohort research
Prospective Cohort Research:
The research groups - families coming for treatment in "Active Maccabi" clinics in the
Northern Region, Israel. Approximately 30 families.
Retrospective Random Controlled Research
1. The research group - families that have completed an intervention program of "Active
Maccabi" Northern Region, Israel,within the past two to three years. The families will
be requested to attend a follow-up meeting of all family members in which they will
answer questionnaires. Approximately 66 families.
2. The control groups - families who did not participate in the program who have a child
between the age 7-14 who has suffered from obesity/weight (over the past 2-3 years), in
correlation with the child in the intervention group. Approximately 66 families.
Hypotheses of the research:
1. Status of the weight of the child being treated and of his siblings will be higher than
that at the end of the program.
2. Indication of the obesogenic environment of families participating in the program will
be lower in comparison with families not participating in the program.
3. The rate of eating disorder symptoms among children who participated in the program will
be lower in comparison with those of the obese/overweight child in families who were not
the program.
4. The rate of eating disorder symptoms among siblings who participated in the program will
be lower than that of siblings in families not in the program.
Duration of the Research -Prospective Cohort Research: 6 months of intervention. 8 months
follow-up.
Research Instruments
1. Anthropometric measurements of all children in the family (height, weight and BMI). BMI
per centile examinations according to age.
2. An acquaintance questionnaire and demographic details - to be answered by parents
3. A FEAQ_R questionnaire to be answered by the parents (only in the prospective research
group). The questionnaire will examine the obesogenic burden in the family. A column
will be added for each sibling of relevant age. The questionnaire will be valid in
English and Hebrew. The psychometric characteristics of the questionnaire: Alpha
cronbach - validity 0.84; Reliability 0.78 Trt
4. Eat-26 (cheat) questionnaire to be answered by the children and their siblings. The
questionnaire will examine the risk of developing an eating disorder.
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