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Enrolling by Invitation

NCT Number: NCT07422909

Bridging the Gap: Implementing BRIDGES

Together with teenagers, we have developed a new approach: BRIDGES, which stands for "In Brussels, Resilience and Inclusion for Depression through Guidance, Exercise, and Support." BRIDGES aims to help young people with depression get moving again in their daily lives, at their own pace and in ways that are good for them.

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Key information

Age range

12 year–19 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

AREA+, Epsylon

Brussels, Uccle, 1180, Belgium

About this study

Even though physical activity is recognized for its mental and physical health benefits, we find that adolescents going through a difficult psychological period often engage in very little of it. Current physical activity offerings do not always take into account their specific needs, preferences, or daily realities. That is why we have co-created a new approach with adolescents: BRIDGES, which stands for "In Brussels, Resilience and Inclusion for Depression through Guidance, Exercise, and Support." This project includes 18 30-minute sessions over 3 months with a physical therapist specializing in mental health, including individual follow-ups with advice and discussions, as well as putting you in touch with sports clubs or associations of your choice. The goal is to help you get moving again in your daily life, at your own pace and in a way that makes you feel good.

This study has a waiting list control group, so young people can either participate immediately or wait 6 months to participate.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All adolescents aged 12 to 19 with a diagnosis of depression who are receiving outpatient care through AREA+
  • voluntary participation and accepting the randomisation
  • being admitted at AREA+
  • being able to stay focused for 30 minutes
  • having a good knowledge of French
  • physically inactive defined as not meeting the PA guidelines from World Health Organisation (28) following the corresponding age (i.e. at least 420 min of moderate to vigorous physical activity (MVPA) /week for those aged 12-17 and at least 150 min of MVPA /week for those aged 18 and 19 years
  • living in Brussels

Exclusion criteria

  • intellectual disability (defined as an intelligence quotient < 70)
  • participants with serious medical problems or medical precautions prohibiting higher-intensity exercise (e.g., severe metabolic disorders, oncologic disease, unstable diabetes) according to the recommendations of the American College of Sports Medicine.

Treatment and study plan

The BRIDGES (In Brussels, Resilience and Inclusion for Depression through Guidance, Exercise and Support) intervention

Behavioral

Described above

Primary outcomes

  1. Depressive symptoms

    Time frame: Throughout the entire study, during approximately 15 months

    Patient Health Questionnaire-9 modified for Adolescents (PHQ-A) The PHQ-A is a brief instrument modified to adolescents used to assess the severity of depression (41). It contains 9 items that are on a scale from 0 to 3, with the total score ranging from 0 to 27.

  2. Physical activity levels

    Time frame: Throughout the entire study, during approximately 15 months

    Physical Activity Vital Sign (PAVS) The PAVS is a screening tool used to assess patients' physical activity levels (37). It consists of two questions: (a) on average, how many days per week do you engage in moderate to vigorous physical activity, and (b) on those days, how many minutes do you typically spend participating in moderate to vigorous physical activity? The product of these responses (days × minutes) provides an estimate of the patient's average weekly minutes of physical activity in moderate to vigorous physical activity.

Secondary outcomes

  1. Depressive symptoms (larger evaluation)

    Time frame: Throughout the entire study, during approximately 15 months

    Beck Depression Index (BDI II) The BDI-II captures specific behavioral manifestations of depression. It is a 21-item self-report inventory, with each item scored from 0 to 3 based on four statements reflecting symptom severity, yielding a total score ranging from 0 to 63.

  2. Multidimensional Scale of Perceived Social Support (MSPSS)

    Time frame: Throughout the entire study, during approximately 15 months

    The Multidimensional Scale of Perceived Social Support (MSPSS) is a widely used self-report instrument designed to assess an individual's perception of social support from different sources (49). The scale comprises 12 items, each rated on a 7-point Likert scale ranging from a score of 7 to 84.

  3. Adapted Exercise self-efficacy (SEE)

    Time frame: Throughout the entire study, during approximately 15 months

    Exercise self-efficacy (SEE) is a key determinant of intention formation and engagement in physical activity. In the original SEE, respondents rate their confidence in exercising three times per week for 20 minutes. For the present study, the scale was adapted so that the target behavior reflects an individualized exercise goal defined by each adolescent, that is, the type of physical activity they wish to perform.

  4. Astrand Rhyming test (ART)

    Time frame: Throughout the entire study, during approximately 15 months

    Astrand Rhyming test (ART) ART is a single-stage cycle ergometer test, to measure the CRF fitness levels (assessed as an estimation of VO2 max)

  5. Waist-to-height ratio (WHtR)

    Time frame: Throughout the entire study, during approximately 15 months

    Waist-to-height ratio (WHtR) WHtR is calculated as waist circumference (cm) divided by height (cm). Waist circumference will be measured in standing position, midway between the lowest border of the rib cage and the superior border of the iliac crest, at the end of a normal expiration.

  6. Motivational interviewing fidelity

    Time frame: Throughout the entire study, during approximately 15 months

    Fidelity to motivational interviewing (MI) will be assessed using a combination of observer- and participant-reported measures. First, adherence to MI principles will be evaluated using the Independent Tape Rater Scale (ITRS), which is recommended for effectiveness studies

  7. Client Perception of Motivational Interviewing

    Time frame: Throughout the entire study, during approximately 15 months

    the Client Perception of Motivational Interviewing (CPMI) scale captures participants' experiences of MI-consistent communication during sessions. This combined approach enables assessment of both the technical and relational components of MI fidelity while remaining feasible within the constraints of a pilot implementation study.

  8. The Health Care Climate Questionnaire

    Time frame: Throughout the entire study, during approximately 15 months

    Adolescents will complete the Health Care Climate Questionnaire (HCCQ) (61) to evaluate perceived autonomy support provided by the physiotherapist. In addition, brief post-session feedback forms will invite participants to rate the extent to which they felt understood, empowered, and supported in setting their own goals-key indicators of SDT-congruent delivery.

  9. Logbook

    Time frame: Throughout the entire study, during approximately 15 months

    the physiotherapist will fill out a logbook with their participation describing their presence, the context, the mechanisms at work, and clinical observations on the adolescents and their participation in physical activities

Other outcomes

  1. Implementation outcomes

    Time frame: Throughout the entire study, during approximately 15 months

    For the implementation assessment, PRISM will provide the overarching conceptual structure to examine organizational, individual, and system-level factors that influence delivery, uptake, and sustainability of the intervention (26). Within this framework, the RE-AIM dimensions (Reach, Effectiveness, Adoption, Implementation, and Maintenance) will be systematically applied (27). Reach will assess the proportion and representativeness of adolescents. Effectiveness will evaluate changes in physical activity, depressive symptoms, and secondary outcomes. Adoption will explore barriers and facilitators to participation and delivery from the perspectives of adolescents, clinicians, and community partners. Implementation will monitor fidelity to motivational interviewing and self-determination theory principles. Maintenance will evaluate the potential for long-term integration of the intervention. Semi-structured interviews guided by PRISM domains will complement quantitative measures.

Sponsors and collaborators

Lead sponsor

Université Catholique de Louvain

Other

Collaborators

  • KU Leuven

Registry information

Official study title

Bridging the Gap: Implementing BRIDGES (Brussels Resilience and Inclusion for Depression - Guidance, Exercise and Support) to Shape Adolescent Outpatient Mental Health Care. A Randomized Control Study Protocol

Acronym: CCEMHA

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Feb 20, 2026
Registry last updated
Jun 18, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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