- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07587372
Reducing Problematic Internet Use and Improving Well-Being in Adolescents Through Online Yoga Meditation: A Randomized Controlled Trial
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
Status
Intervensjon / Behandling
Detaljert beskrivelse
Studietype
Registrering (Faktiske)
Fase
- Ikke aktuelt
Kontakter og plasseringer
Studiesteder
-
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Virginia
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Chantilly, Virginia, Forente stater, 20151
- Sahaja Yoga Meditation Virginia
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Barn
- Voksen
Tar imot friske frivillige
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
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
Sponsor
Samarbeidspartnere
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Faktiske)
Studiet fullført (Faktiske)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Andre studie-ID-numre
- TCM_SYM_2025
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
IPD-planbeskrivelse
IPD-delingstidsramme
Tilgangskriterier for IPD-deling
IPD-deling Støtteinformasjonstype
- STUDY_PROTOCOL
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Studerer et amerikansk FDA-regulert enhetsprodukt
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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