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HELP (HEalthy Lifestyles Project) for Youth With Mental Distress

HELP (HEalthy Lifestyles Project) for Youth With Mental Distress E-Health Intervention: Patient and Healthcare Impacts

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06232733
Acronym
HELP
Enrollment
130
Registered
2024-01-31
Start date
2024-06-15
Completion date
2028-12-31
Last updated
2026-08-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mental Health Issue

Keywords

adolescent, healthy lifestyle behavior

Brief summary

The goal of this clinical trial is to learn about how healthcare providers can support youths' mental health. The main question\[s\] it aims to answer are: * Do youth (12 to 17 years of age) who engage in the 6-month HELP e-intervention have a larger improvement in emotional health (measured by the Strengths and Difficulties Questionnaire) than youth who do not receive the intervention? * Does engagement in the HELP e-intervention improve lifestyle behaviour (physical activity, sleep or screen time)? * Do youth who engage in the 6-month HELP e-intervention utilize fewer mental healthcare resources, during and for 1 year following study participation, than youth who do not receive the intervention? Participants will receive the HELP intervention for 6 months, either immediately or after waiting 6 months from study enrollment. At 0, 3, 6, and 12 months, participants will answer a series of questionnaires to assess their emotional health and lifestyle behaviors. Researchers will compare the emotional health and lifestyle behaviors of youth who received HELP immediately to those who wait for 6 months prior to the intervention to see if their emotional health or lifestyle behaviors differ.

Detailed description

This study will evaluate the efficacy of 6 months of HELP e-intervention access with kinesiologist support in a randomized controlled trial to determine if the changes in emotional health (primary outcome) and lifestyle behaviors (secondary outcomes) differ from changes among youth with delayed intervention access (control condition). Sustainability of the intervention will be assessed for an additional 6 months. Participants will be youth 12-17 years of age who contact youth mental health services. The unique HELP e-resources developed by the research team utilize age-appropriate graphics and interactive formats developed collaboratively with youth/parent/clinician partners. There are 4 sections: 1) Know Your Habits, 2) Physical Activity, 3) Screen Time, 4) Sleep. A kinesiologist will support participants in the intervention. Study assessments will be completed by researchers blind to study group allocation. Researchers will also evaluate the impact of the HELP e-intervention on the use of mental healthcare services, the need for mental health professional support of lifestyle behaviors and the association between self-reported and objectively measured lifestyle behaviors. It is hypothesized that youth engaging in the HELP e-intervention will have improved emotional health and enhanced lifestyle behaviors in comparison to those receiving the delayed (post 6-months) intervention. It is also hypothesized that changes during the intervention will be maintained for an additional 6 months, and that self-reported measures will accurately reflect objective measurements. Finally, it is hypothesized that youth engaging in the HELP e-intervention will require fewer youth mental health supports, and when supported will be less likely to require treatment directed at lifestyle behaviors.

Interventions

BEHAVIORALHealthy Lifestyles Project e-intervention

Virtual lifestyle behaviour change support.

Sponsors

Children's Hospital of Eastern Ontario
Lead SponsorOTHER
Children's Hospital Academic Medical Organization (CHAMO)
CollaboratorUNKNOWN

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

It is not possible to blind the participants or families to the study group allocation. Investigators will support delivery of the intervention.

Intervention model description

Immediate or delayed intervention

Eligibility

Sex/Gender
ALL
Age
12 Years to 17 Years
Healthy volunteers
No

Inclusion criteria

* Youth 12-17 years of age seeking, waiting for or receiving support for emotional distress. * Able to provide informed consent to study participation. * Able to engage in the HELP e-intervention in English (French translation of the e-modules will not be available until intervention efficacy is established). * Willing to be randomized to a study group. * Willing to complete objective behaviour measures if selected (1 of 3 participants). * Willing to complete the study questionnaires. * Willing to provide consent for evaluation of mental healthcare system outcomes via their health record.

Exclusion criteria

* Identified or suspected eating disorder * Youth whose health or family status is deemed to be inappropriate for the study as per their most responsible clinician.

Design outcomes

Primary

MeasureTime frameDescription
Strengths and Difficulties Questionnaire6 monthsYouth emotional distress. Minimum score 0. Maximum Score 50. Higher score is lower emotional health.

Secondary

MeasureTime frameDescription
Habitual Activity Estimation Scale6 monthsSelf-reported daily physical activity. Minutes and proportion of day spent inactive, somewhat inactive, somewhat active and active for weekend and week days.
Adolescent Sleep Hygiene Scale6 monthsSelf-reported sleep habits. Minimum score 33. Maximum score 198. Higher score is better sleep hygiene.
Adolescent Sedentary Activity Questionnaire6 monthsSelf-reported screen time (hours and minutes).

Countries

Canada

Contacts

PRINCIPAL_INVESTIGATORClare Gray, MD

Children's Hospital of Eastern Ontario

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 25, 2026