Effectiveness of a 10-week Multicomponent Intervention Combined With Parent Education on Binge Eating Behavior in Children and Adolescents

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age7-14
SponsorUniversity of Aarhus

About this trial

The main purpose is to investigate the effectiveness of a 10-week multicomponent camp intervention to reduce BE behavior in children and adolescents and explore in a randomized controlled setting if a parent-based BED-intervention has any add-on effect, attenuating the development of BE behavior in this sample. The study will include an initial follow-up assessment scheduled 10-12 weeks after camp completion and plans for long-term follow-up assessments one, three and five years after inclusion.

Overall, we hypothesize that the multicomponent camp intervention will effectively reduce BE behavior in children and adolescents. Furthermore, we hypothesize that participants whose parents are randomized to receive the parental BED intervention will show a lower prevalence of BE behavior one year after the camp intervention compared with children whose parents receive standard care.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Attending the camp in Hobro or Fjordmark from January 2027 to December 2027

7-14 years of age at recruitment

Participants must have written informed consent from parent/guardian before camp to participate

At least one parent/guardian submit written informed consent to participate in the study with their child

Disqualifiers

A medical condition affecting dietary intake and/or eating behavior

Taking weight loss medication

The parent/guardian don't understand the written informed consent

Participant or parent/guardian are unwilling to or unable to comply with the study protocol and instructions given by the study staff.

Trial design

Design model

Parallel

Treatments tested in this trial

  • A 10-week multicomponent camp intervention for children

    Behavioral

    A 10-week multicomponent camp intervention for participating children only, focusing on social and physical activities, healthy meals, and daily physical activities.

  • A BED intervention for parents

    Behavioral

    An add-on virtual parent-based intervention providing knowledge about BED and tools to support their child's eating after the multicomponent camp intervention.

Treatment groups

200 Participants
are divided into 2 treatment groups
Group A: Standard parent involvement during camp (P-ST)Active comparator 1 intervention
Group B: Add-on parent-based BED intervention during camp (P-BED)Experimental treatment 2 interventions

Trial outcomes

Primary outcomes

1

Changes in Binge eating behavior using the STOB-screening tool

The STOB-screening tool consist of five yes/no questions + one question about number of overeating episodes

Time frame
Baseline, 10-weeks (post-intervention), 10-12 weeks after the intervention, and 1, 3 and 5 years after the intervention.
2

Changes in prevalence of Binge eating disorder (BED) using the ChEDE

Binge eating disorder will be assessed using the Child Eating Disorder Examination interview

Time frame
Baseline, and 10-weeks (post-intervention).

Secondary outcomes

1

Changes in Body Mass Index standard deviation score (BMI-SDS)

BMI-SDS calculated using World Health Organization Anthro-Plus software/cutoffs to define normal weight, overweight and obesity among participants.

Time frame
Baseline, 10-weeks (post-intervention), 10-12 weeks after the intervention, and 1, 3 and 5 years after the intervention.
2

Changes in Body fat (%)

Measured in light clothing without shoes using a Bioelectric impedance (InBody model 270, Hopkins Medical Products, Grand Rapids, MI, USA).

Time frame
Baseline, 10-weeks (post-intervention), and 1, 3 and 5 years after the intervention.
3

Changes in Skeletal Muscle Mass (kg)

Measured in light clothing without shoes using a Bioelectric impedance (InBody model 270, Hopkins Medical Products, Grand Rapids, MI, USA).

Time frame
Baseline, 10-weeks (post-intervention), and 1, 3 and 5 years after the intervention.

Other outcomes

1

Changes in Quality of Life using the PedsQL

Quality of life (QoL) will be assessed using the Pediatric Quality of Life Inventory to assess total QoL, physical functioning, emotional functioning. social functioning, and school functioning.

Time frame
Baseline, 10-weeks (post-intervention), 10-12 weeks after the intervention, and 1, 3 and 5 years after the intervention.
2

Changes in appetitive traits using the CEBQ or AEBQ depending on age

Appetitive traits will be measured using the Children's eating behavior questionnaire or Adult Eating behavior questionnaire depending on age to assess food responsiveness, emotional overeating/undereating, enjoyment of food, desire to drink, hunger, satiety responsiveness, slowness in eating, and food fussiness.

Time frame
Baseline, 10-weeks (post-intervention), 10-12 weeks after the intervention, and 1, 3 and 5 years after the intervention.

Sponsors and contacts

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