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Impact of Device Free Summer Camp on Adolescent Mental Health and Wellbeing

19. august 2026 opdateret af: Sapien Labs

IMPACT OF DEVICE FREE SUMMER CAMP ON ADOLESCENT MENTAL HEALTH AND WELLBEING

The goal of this clinical trial is to understand if attendance of a device-free summer camp, representing a shift from a digital environment to one that is device free and involves in person social interaction, can change mental health status and brain physiology in teens age 12-17. The main question it aims to answer is:

  • How much is aggregate mental health and its various dimensions and components changed at the end of the camp attendance relative to the start of camp.
  • How much is brain physiology, as measured by EEG change, changed at the end of camp relative to the start of camp.

Participants are recruited from among teens signed up to attend 2 or 3.5 week sessions a summer camp in Maine.

Studieoversigt

Status

Afsluttet

Betingelser

Detaljeret beskrivelse

The goal of this clinical trial is to understand if attendance of a device-free summer camp, representing a shift from a digital environment to one that is device free and involves in person social interaction, can change mental health status and brain physiology in teens age 12-17. The main question it aims to answer is:

  • How much is aggregate mental health and its various dimensions and components changed at the end of the camp attendance relative to the start of camp.
  • How much is brain physiology, as measured by EEG change, changed at the end of camp relative to the start of camp.

Participants are recruited from among teens signed up to attend 2 or 3.5 week sessions a summer camp in Maine. Participants were asked to complete the MHQ, a comprehensive mental health assessment spanning 47 emotional, social and cognitive aspects and on the first day of camp and then again on the day before departure. In addition participants were asked questions on their school and camp experiences at the start and end of camp respectively.

Participants were also invited to participate in a socio-emotional task and/or have EEG measurements read on the first day of camp and the day before departure form camp. The socio-emotional task involved speaking or performing in front of a group of 4 or 5 people and rating one's own feelings performing this task as well as rating the perceived feelings of other group members when they were performing the task.

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

333

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

    • Maine
      • Porter, Maine, Forenede Stater, 04068
        • Maine Teen Camp

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Barn

Tager imod sunde frivillige

Ja

Beskrivelse

Inclusion Criteria:

  • Attendance of Maine Teen Camp sessions during summer months of 2024 and 2025.

Exclusion Criteria:

  • None

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Forebyggelse
  • Tildeling: N/A
  • Interventionel model: Enkelt gruppeopgave
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Maine Teen Camp attendees
Attendance of a residential device-free summer camp for teens for 2 to 3.5 weeks characterized by in-person interaction and nature rich outdoor activities.
Attendance of a residential device-free summer camp in Maine for 2-3.5 weeks.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Change from Baseline in Mental Health Quotient (MHQ) at End of Camp
Tidsramme: Baseline (Day 1) to end of camp attendance (up to 3.5 weeks).
The Mental Health Quotient or MHQ is an aggregate score of mental health computed from the 47 items of the MHQ assessment. The score ranges from -100 to +200, where higher scores indicate better mental health outcomes. Negative scores indicate significant symptoms that impact function (Distressed/Struggling range), while positive scores reflect the wide range of normal function (Enduring to Thriving). Change is calculated by subtracting the baseline score from the end of camp score.
Baseline (Day 1) to end of camp attendance (up to 3.5 weeks).

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Change from Baseline in Ratings of 47 MHQ Items After Camp Attendance
Tidsramme: Baseline (Day 1) to end of camp attendance (up to 3.5 weeks).
Difference in the ratings of each of the 47 items in the MHQ assessment spanning emotional, social, cognitive and physical capacities and problems. Participants rate each item on a 9-point life impact scale.
Baseline (Day 1) to end of camp attendance (up to 3.5 weeks).
Change from Baseline in Resting-State Electroencephalography (EEG) measures
Tidsramme: Baseline (Day 1 of camp) and Post-Intervention (Final day of camp - 2.5-3 weeks later)
The outcome measure evaluates changes in EEG spectral metrics such as spectral slope, spectral bands and time domain metrics such as complexity/entropy measures such as Detrending Fluctuation Analysis (DFA), Lempel-Ziv Complexity and Sample Entropy measured during 3 minutes of EEG with eyes closed at the start and end of the camp session.
Baseline (Day 1 of camp) and Post-Intervention (Final day of camp - 2.5-3 weeks later)

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Sponsor

Efterforskere

  • Ledende efterforsker: Tara Thiagarajan, PhD, Sapien Labs

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

1. juli 2024

Primær færdiggørelse (Faktiske)

17. august 2025

Studieafslutning (Faktiske)

17. august 2025

Datoer for studieregistrering

Først indsendt

6. august 2026

Først indsendt, der opfyldte QC-kriterier

11. august 2026

Først opslået (Faktiske)

12. august 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

21. august 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

19. august 2026

Sidst verificeret

1. august 2026

Mere information

Begreber relateret til denne undersøgelse

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

JA

IPD-planbeskrivelse

Anonymized assessment and questionnaire responses and raw EEG files

IPD-delingstidsramme

August 2026 onwards (no end date)

IPD-delingsadgangskriterier

Any researcher with stated legitimate research intent will be able to access the anonymized date and supporting information upon submitting an email request to the PI.

IPD-deling Understøttende informationstype

  • STUDY_PROTOCOL
  • ICF

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