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Online Sleep Education for College Student's Sleep Health and Executive Functioning

10. august 2026 oppdatert av: Kiley Hawkins, Northern Arizona University

The Role of Sleep Education in Improving Sleep Quality, Executive Functioning, and Sleep Health Literacy

The goal of this clinical trial is to determine if asynchronous psychoeducational sleep intervention works to improve college students' levels of self-reported sleep health literacy, sleep quality, and executive functioning.

The main questions it aims to answer are:

Can an educational sleep intervention improve college students' sleep health literacy and sleep quality? Does improved sleep health literacy impact sleep quality? Does improved sleep improve executive functioning in a college student sample?

The hypotheses of the present study include the following:

  • College students with poor sleep quality will have lower executive functioning
  • College students who participate in a brief educational sleep intervention will have more improvements in sleep health literacy compared to college students who do not
  • College students who participate in a brief educational sleep intervention will have more improvements in sleep quality compared to college students who do not
  • College students who participate in a brief educational sleep intervention will have more improvements in executive functioning compared to college students who do not.

Researchers will compare the intervention group to a wait-list control group to see if college students who watch the psychoeducational sleep intervention have more improvements in sleep quality, sleep health literacy, and executive functioning than those who do not.

Participants will:

  • Complete a pre-intervention survey
  • Respond to a post-intervention survey six weeks after the pre-intervention survey
  • Be randomly assigned to watch a 30-to 45-minute psychoeducational sleep lecture video either during the pre-intervention survey or after the post-intervention survey

Studieoversikt

Status

Har ikke rekruttert ennå

Studietype

Intervensjonell

Registrering (Antatt)

300

Fase

  • Ikke aktuelt

Kontakter og plasseringer

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

Studiekontakt

  • Navn: Kiley D Hawkins, B.S.
  • Telefonnummer: 623-241-2334
  • E-post: kh2874@nau.edu

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

  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Ja

Beskrivelse

Inclusion Criteria:

  • Be at least 18 years old
  • Be currently enrolled as an undergraduate student in a U.S. college or university
  • Have English language proficiency
  • Have internet access
  • Have an electronic device to complete an online survey

Exclusion Criteria:

  • Having a diagnosed sleep-wake disorder
  • Having a history of treatment for sleep difficulties

Studieplan

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

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Annen
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Ingen inngripen: Wait-List Control Group
The wait-list control group will not receive the 30-to 45-minute psychoeducational sleep lecture video prior to completing post-intervention surveys. Participants assigned to this arm will be granted access to the intervention at the conclusion of the post-intervention survey.
Eksperimentell: Psychoeducational Sleep Intervention
Participants assigned to this arm will undergo a 30-to 45-minute psychoeducational sleep lecture video. This video will be embedded in the pre-intervention survey packet.
The present study uses a 30-to 45-minute psychoeducational sleep lecture that is tailored to college students. The lecture reviews topics such as sleep information, trends among college students, and consequences of poor sleep (e.g., on psychosocial, cognitive, and academic functioning). The lecture also includes information about sleep hygiene and stimulus control instructions to provide students with resources for implementing adaptive sleep hygiene behaviors that promote better sleep and functioning. This intervention will be embedded within the pre-intervention survey packet for participants who are randomly assigned to the intervention arm. Participants assigned to the no intervention arm will be granted access to the intervention at the conclusion of the post-intervention survey packet.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Pittsburgh Sleep Quality Index
Tidsramme: This will be administered at enrollment (pre-intervention), and again in 6-weeks (post-intervention)
This is a 19-item self-report questionnaire used to assess sleep quality, sleep onset latency, total duration, sleep efficiency, sleep disturbances, use of sleep medications, and daytime dysfunction.
This will be administered at enrollment (pre-intervention), and again in 6-weeks (post-intervention)
Barkely Deficits in Executive Functioning-Short Form
Tidsramme: This will be administered at enrollment (pre-intervention), and again in 6-weeks (post-intervention)
This is a 20-item self-report questionnaire that measures deficits in time management, organization, problem solving, self-restraint, self-motivation, and emotion regulation.
This will be administered at enrollment (pre-intervention), and again in 6-weeks (post-intervention)
Sleep Health Literacy Scale
Tidsramme: This will be administered at enrollment (pre-intervention), and again in 6-weeks (post-intervention)
This is a 61-item self-report questionnaire used to measure sleep health communication and sleep health knowledge.
This will be administered at enrollment (pre-intervention), and again in 6-weeks (post-intervention)

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Behavior Change Questions
Tidsramme: This will be administered at enrollment (pre-intervention), and again in 6-weeks (post-intervention)
These are questions developed by the researcher to assess participants' perceptions of their sleep, knowledge of sleep and sleep hygiene, and their ability to manage day-to-day tasks. These questions will also inquire about specific behavioral/sleep hygiene changes participants intend to make and any barriers to implementing the changes.
This will be administered at enrollment (pre-intervention), and again in 6-weeks (post-intervention)

Samarbeidspartnere og etterforskere

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

Etterforskere

  • Studiestol: Marie-Christine Goodworth, PhD, Northern Arizona University
  • Hovedetterforsker: Kiley D Hawkins, B.S., Northern Arizona University

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Generelle publikasjoner

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 (Antatt)

1. september 2026

Primær fullføring (Antatt)

1. desember 2026

Studiet fullført (Antatt)

1. mai 2027

Datoer for studieregistrering

Først innsendt

10. august 2026

Først innsendt som oppfylte QC-kriteriene

10. august 2026

Først lagt ut (Faktiske)

14. august 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

14. august 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

10. august 2026

Sist bekreftet

1. august 2026

Mer informasjon

Begreper knyttet til denne studien

Ytterligere relevante MeSH-vilkår

Andre studie-ID-numre

  • 2441114-2

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

IPD-planbeskrivelse

IPD will not be shared to preserve participant confidentiality, as outlined in the informed consent document.

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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