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CompletedNCT04642222Updated May 25, 2023

APOLO-Teens, a Web-based Intervention For Adolescents With Overweight/Obesity

An interventional study of APOLO-Teens web-based intervention and Treatment as Usual for Pediatric Obesity in Pediatric Obesity, sponsored by University of Minho. Completed at 2 sites in Portugal. Open to participants aged 13 Years to 18 Years. Per ClinicalTrials.gov, last updated 2023-05-25.

Sponsored by University of Minho · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 5 years 1 month after the study started (first participant enrolled Oct 2015, registered Nov 2020).
Phase
Not applicable
Study type
Interventional
Enrollment
240
Allocation
Randomized
Ages
13 Years to 18 Years
Sex
All
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Study summary

With the demand for weight-loss interventions likely to continue its upward trend over the next decades, the question remains on how to continuously monitor and support overweight and obese adolescents, particularly in the long-term. Moreover, as the burden of the obesity rates increases in health care centers, the development of alternative delivering strategies gains attention. In an environment of limited resources, the development of new-technology based programs seems a promising area to deliver cost-effective interventions to a wide number of individuals. However, the existing studies present several limitations and a challenging aspect of treating obesity in adolescents is the presence of high rates of disordered eating behaviors.

The objective of this study is to develop and test the effectiveness of a web-based Cognitive Behavioral Therapy intervention, for adolescents with overweight/obesity. A Randomized Controlled Trial will compare a control group receiving medical treatment as usual (TAU), and an intervention group receiving TAU plus a psychological/behavioral intervention delivered via the internet.

Read the detailed description

This research project intends to examine the effectiveness of a Cognitive Behavioral Therapy and psychoeducational based program for adolescents with overweight and obesity delivered as a web-based intervention: APOLO-Teens. Therefore, a randomized controlled trial will compare a control group receiving medical treatment as usual for pediatric obesity in public health care centers in Portugal, and an intervention group receiving TAU plus the APOLO-Teens web-based intervention.

The APOLO-Teens web-based intervention was designed to optimize treatment as usual for pediatric obesity, promoting the adoption of healthy eating habits and lifestyle behaviors. Particularly it aims to promote higher consumption of fruits and vegetables, increase physical activity levels, reduce sedentary time, enhance psychological well-being, and facilitating weight loss.

All participants will be assessed at baseline, 3 months after the beginning of the research protocol/intervention, end of the web-based intervention, and at 6 and 12 months follow-up. All the assessments will be conducted in Qualtrics: Online Survey Software. Repeated Paired Samples T-test will explore differences between the two groups across the assessment times. Multiple linear regression analysis will be applied to explore predictors of weight loss and weight regain, and survival analyses to identify participants with the highest probability to regain weight. Additionally, 3-Level Hierarchical Linear Models will be conducted to explore the temporal occurrence and patterns of change of eating-related variables, physical activity, and BMI z-score in participants from the two groups.

It is expected that the intervention group participants will present a higher frequency of healthy food consumption (fruit/vegetables) and increased physical activity levels at the end of the web-based intervention when compared with TAU group participants. We further expect, differences between the groups regarding eating behavior-related variables, as well as in the psychological features assessed throughout the different assessment points, and ultimately in weight maintenance or regain, with the intervention group presenting lower scores/weight.

02

Conditions studied

  • Pediatric Obesity

Keywords

  • Adolescent
  • Web-based intervention
  • Health promotion
  • Eating Behaviors
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In context

Obesity

6,297 studies on the registry are indexed under Obesity; 1,693 are open to participants now.

This study's enrollment of 240 is above the median of 78 across 4,879 interventional studies indexed under Obesity.

Browse Obesity studies →

Lead sponsor

University of Minho is the lead sponsor of 37 studies on the registry; 9 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
13 Years to 18 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Participants with overweight or obesity (BMI z-score ≥ 1/BMI percentile ≥ 85th);
  • Enrolled in ambulatory treatment for overweight/obesity in a public Portuguese health care center;
  • Having a Facebook® account;
  • Having access to the Internet at least three times per week.

Exclusion criteria

Exclusion Criteria:

  • Medical conditions that affect weight;
  • Intellectual disabilities (Specific learning difficulties that prevented adolescents from reading and understanding written text);
  • Ambulatory movement limitations (e.g., use of the walking stick, morpho-functional alterations as lower limb amputation, etc.);
  • Not being under other interventions for weight loss at the time of enrollment.
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
240 participants (actual)

Study arms

  • Experimental
    APOLO-Teens Intervention Group (APOLO-Teens group)

    In addition to the Treatment As Usual for pediatric obesity offered in Portuguese public hospitals, participants in this group receive the APOLO-Teens web-based intervention. It comprises three key components: 1) a manualized psychoeducational intervention implemented via Facebook® private groups, including cognitive-behavioral therapy strategies; 2) A weekly self-monitoring system (the APOLO-Teens web application) with automatic feedback messages assessing hours of physical activity, sedentary time, and consumption of fruits and vegetables; and 3) Monthly chat sessions.

    Behavioral: APOLO-Teens web-based intervention

  • Active comparator
    Treatment As Usual (TAU) Control Group (TAU control group)

    Treatment As Usual control group receives the standard intervention for pediatric obesity offered in Portuguese public hospitals. It comprises pediatric or/and nutritional appointments, usually a 30-minute appointment every 3 months. These appointments usually include a physical examination (weight, height) and personalized dietary/lifestyle recommendations. The Treatment As Usual intervention is common to the APOLO-Teens group and TAU control groups.

    Other: Treatment as Usual for Pediatric Obesity

Interventions

  • BehavioralAPOLO-Teens web-based intervention

    The APOLO-Teens web-based intervention is a 6-month cognitive-behavioral lifestyle program developed to optimize treatment as usual for pediatric obesity in public portuguese hospitals.

  • OtherTreatment as Usual for Pediatric Obesity

    Treatment as Usual for pediatric obesity in portuguese public hospitals.

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What researchers measure

Primary outcomes

  1. Foods/beverages intake

    Food/beverages frequency questionnaire, which assesses the frequency of soup, fruit, vegetables on the plate, sweetened beverages drinks and pastries/sweets intake in the previous week.

    Time frame: Change from baseline, to 3 months after the begging if the intervention, end of intervention (after 6-months of baseline assessment), 6 and 12 months follow-up. Specific duration of time over which participant change is assessed: 18 months.

  2. Minutes of moderate-to-vigorous physical activity per week at school

    Youth Activity Profile (YAP): This is a 15 items questionnaire to evaluate psychical activity and sedentary behaviors in youth on the previous seven days.

    Time frame: Change from baseline, to 3 months after the begging if the intervention, end of intervention (after 6-months of baseline assessment), 6 and 12 months follow-up. Specific duration of time over which participant change is assessed: 18 months.

  3. Minutes per week spent in sedentary behaviors

    Youth Activity Profile (YAP): This is a 15 items questionnaire to evaluate psychical activity and sedentary behaviors in youth on the previous seven days.

    Time frame: Change from baseline, to 3 months after the begging if the intervention, end of intervention (after 6-months of baseline assessment), 6 and 12 months follow-up. Specific duration of time over which participant change is assessed: 18 months.

  4. Minutes of moderate-to-vigorous physical activity out-of-school per week

    Youth Activity Profile (YAP): This is a 15 items questionnaire to evaluate psychical activity and sedentary behaviors in youth on the previous seven days.

    Time frame: Change from baseline, to 3 months after the begging if the intervention, end of intervention (after 6-months of baseline assessment), 6 and 12 months follow-up. Specific duration of time over which participant change is assessed: 18 months.

Secondary outcomes

  1. Eating disturbance

    Children's Eating Attitudes Test (ChEAT). Higher scores indicate more eating disturbance.

    Time frame: Baseline (before the intervention), 3 months after the begging if the intervention, end of intervention (after 6-months of baseline assessment), 6 and 12 months follow-up. Specific duration of time over which participant is assessed: 18 months.

  2. Grazing eating pattern

    Repetitive Eating Questionnaire (Rep(eat)-Q). Higher scores indicate the existence of a grazing-type eating pattern.

    Time frame: Baseline (before the intervention), 3 months after the begging if the intervention, end of intervention (after 6-months of baseline assessment), 6 and 12 months follow-up. Specific duration of time over which participant is assessed: 18 months.

  3. Psychological Distress (depression, anxiety and stress)

    Depression Anxiety Stress Scales (DASS-21). Higher scores indicating more anxiety, stress and depressive symptomatology.

    Time frame: Baseline (before the intervention), 3 months after the begging if the intervention, end of intervention (after 6-months of baseline assessment), 6 and 12 months follow-up. Specific duration of time over which participant is assessed: 18 months.

  4. Health-related quality of life

    Pediatric Quality of Life Inventory. Higher scores indicate more health-related quality of life.

    Time frame: Baseline (before the intervention), 3 months after the begging if the intervention, end of intervention (after 6-months of baseline assessment), 6 and 12 months follow-up. Specific duration of time over which participant is assessed: 18 months.

  5. BMI z-score

    Calculated by WHO Anthroplus software 3.2.2. version

    Time frame: Baseline (before the intervention), 3 months after the begging if the intervention, end of intervention (after 6-months of baseline assessment), 6 and 12 months follow-up. Specific duration of time over which participant is assessed: 18 months.

07

Study locations

2 sites
  • Centro Hospitalar Universitário do Porto (Centro Materno Infantil do Norte)
    Porto, 4050-651, Portugal
  • Centro Hospitalar Universitário de São João
    Porto, 4200-319, Portugal
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References and documents

Publications

  • Ramalho S, Saint-Maurice PF, Silva D, Mansilha HF, Silva C, Goncalves S, Machado P, Conceicao E. APOLO-Teens, a web-based intervention for treatment-seeking adolescents with overweight or obesity: study protocol and baseline characterization of a Portuguese sample. Eat Weight Disord. 2020 Apr;25(2):453-463. doi: 10.1007/s40519-018-0623-x. Epub 2018 Dec 5. PubMed 30519810 ↗

Individual participant data

Plan to share: No — The type of data to collect include sensitive and personal health information protected by the Portuguese Law.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 25, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04642222
Lead sponsor
University of Minho
Responsible party
Eva Conceição (Research Fellow, University of Minho) — Principal investigator
First posted
Nov 24, 2020
Start date
Oct 1, 2015
Primary completion
Mar 2022
Completion
Mar 2022
Last update
May 25, 2023

Study contacts

Eva M Conceição, Ph.D.
principal investigator · University of Minho, School of Psychology

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in May 2023. You cannot join it, but the record below documents what was studied.

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