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Reducing Problematic Internet Use and Improving Well-Being in Adolescents Through Online Yoga Meditation: A Randomized Controlled Trial

7. mai 2026 oppdatert av: Tilburg University

This randomized controlled trial investigated the effects of an online Sahaja Yoga meditation program on problematic internet use, mental well-being, self-esteem, and psychological distress among adolescents and youth in the United States. Participants aged 12-18 years were randomly assigned to either a six-week online meditation intervention or a waitlist control group. The meditation sessions were delivered online by experienced adolescent practitioners of Sahaja Yoga meditation under adult supervision.

All participants completed standardized self-report questionnaires before and after the intervention period. The study examined whether participation in the meditation program was associated with improvements in mental well-being and self-esteem, as well as reductions in problematic internet use and psychological distress. A follow-up assessment was also conducted for participants in the intervention group.

Studieoversikt

Detaljert beskrivelse

Adolescents today experience increasing levels of stress, anxiety, social pressure, and excessive internet and social media use, which may negatively affect emotional well-being and daily functioning. Meditation-based interventions were considered a potentially accessible, low-cost, and non-pharmacological approach to supporting adolescent mental health and emotional resilience. The findings of this study were expected to contribute to the development of school- and community-based mental health promotion programs for young people.

Studietype

Intervensjonell

Registrering (Faktiske)

204

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • Virginia
      • Chantilly, Virginia, Forente stater, 20151
        • Sahaja Yoga Meditation Virginia

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Barn
  • Voksen

Tar imot friske frivillige

Ja

Beskrivelse

Inclusion Criteria:

i) school going; ii) able to commit to meditation four times a week during a period of six consecutive weeks.

Exclusion Criteria:

i) currently in treatment for several psychological problems, including trauma and addiction problems ii) already meditating on a regular basis.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Forebygging
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Enkelt

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Sahaja Yoga Meditation Group
Participants received a 6-week online Sahaja Yoga meditation program consisting of four sessions per week.
A 6-week online Sahaja Yoga meditation program consisting of 24 guided meditation sessions delivered four times per week.
Annen: Waitlist Control Group
Participants did not receive the intervention during the initial 6-week study period and completed outcome assessments only. After post-test assessment, they received the meditation program.
Participants served as a waitlist control group during the initial 6-week study period and received the intervention after completion of the post-test assessment.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Problematic internet use
Tidsramme: "From enrollment to the end of invention periode at 12 weeks"
Problematic internet use was measured using the Generalized Problematic Internet Use Scale 2 (GPIUS-2), a 15-item self-report questionnaire designed to assess problematic internet use (Caplan, 2010). The scale measures the subdimensions: 1) preference for online social interaction; 2) mood regulation, 3) cognitive preoccupation; 4) compulsive internet use; 5) negative outcomes, each with three items. Each item is rated on an 8-point Likert scale ranging from 1 (definitely disagree) to 8 (definitely agree), with higher scores indicating greater levels of problematic internet u
"From enrollment to the end of invention periode at 12 weeks"

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Mental well-being
Tidsramme: "From enrollment to the end of invention periode at 12 weeks"
Mental well-being was measured by the Mental Health Continuum-Short Form (MHC-SF), a 14-item questionnaire that measures emotional well-being (three items), social well-being (five items), and psychological well-being (six items) (Lamers, 2015). Participants were asked to indicate their level of well-being over the past four weeks. Each item was rated on a scale from 0 (never) to 5 (every day), with a higher score indicating a higher level of well-being. Cronbach's alpha indicated excellent internal consistency of the scale at both measurement occasions, with α = .91 at pretest and α = .90 at post-test.
"From enrollment to the end of invention periode at 12 weeks"

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Samarbeidspartnere

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

2. februar 2025

Primær fullføring (Faktiske)

7. september 2025

Studiet fullført (Faktiske)

7. september 2025

Datoer for studieregistrering

Først innsendt

7. mai 2026

Først innsendt som oppfylte QC-kriteriene

7. mai 2026

Først lagt ut (Faktiske)

14. mai 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

14. mai 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

7. mai 2026

Sist bekreftet

1. mai 2026

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

JA

IPD-planbeskrivelse

Individual participant data (IPD) underlying the results reported in this study, after de-identification, will be available upon reasonable request to the principal investigator after publication of the main study results. Data will be shared for scientific research and educational purposes.

IPD-delingstidsramme

September 2025 to September 2035

Tilgangskriterier for IPD-deling

Access will be provided through a secure data-sharing procedure in accordance with institutional and ethical guidelines.

IPD-deling Støtteinformasjonstype

  • STUDY_PROTOCOL

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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