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Sleep, Chronotype, and Prosocial Allocation Decisions (SCPAD)

6 luglio 2026 aggiornato da: Dr YU Cehao, The Hong Kong Polytechnic University

Associations Between Sleep Quality, Circadian Timing, and Prosocial Allocation Decisions in Adults

This observational behavioural study examines whether individual differences in sleep quality, sleep timing, and chronotype are associated with prosocial allocation decisions in adults. Participants will complete self-report sleep and circadian questionnaires, including the Pittsburgh Sleep Quality Index and the Munich Chronotype Questionnaire, a 7-day sleep diary, and a brief computer-based Dictator Game allocation task.

The study does not involve sleep deprivation, sleep restriction, treatment, clinical diagnosis, medication, or medical devices. Participants will not be asked to change their sleep schedule. The Dictator Game decisions are hypothetical and do not affect participants' compensation. The study is intended to describe associations between naturally occurring sleep-related individual differences and behavioural allocation choices, not to diagnose or treat sleep or mental health conditions.

Panoramica dello studio

Descrizione dettagliata

This is a non-clinical observational behavioural study of adults aged 18 years or above. The study investigates whether naturally occurring differences in subjective sleep quality, sleep timing, and circadian preference are associated with prosocial decision-making in a computer-based allocation task.

Participants will first provide informed consent and will be assigned a participant code so that research data can be pseudonymised. They will complete demographic questions and sleep-related self-report measures. These measures include the Pittsburgh Sleep Quality Index, which assesses subjective sleep quality over the previous month, and the Munich Chronotype Questionnaire, which assesses sleep timing on workdays and free days and provides chronotype-related variables. Participants will also complete a 7-day sleep diary recording daily sleep-related information such as bedtime, estimated sleep onset, wake time, rise time, naps, subjective sleep quality, and schedule-related information.

Prosocial allocation behaviour will be assessed using a brief computer-based Dictator Game task. In this task, participants make hypothetical allocation choices involving distributions of money between themselves and another party. No deception cover story will be used. Participants will not be falsely told that they are interacting with a real paired participant if no real allocation exists. Dictator Game choices are hypothetical and do not affect actual compensation.

The primary aim is to examine associations between sleep quality, sleep timing, chronotype-related measures, and prosocial allocation behaviour. Secondary analyses may explore whether 7-day sleep diary measures provide additional information beyond retrospective questionnaire measures. Exploratory analyses may examine whether chronotype, sleep timing, or time of day moderates associations between sleep-related measures and Dictator Game behaviour. These analyses will be interpreted cautiously and will not be used to make clinical claims.

The study is not designed to diagnose, treat, or induce any sleep disorder, mental health condition, or other clinical condition. The PSQI, MCTQ, and sleep diary are used as non-diagnostic research measures. No clinical diagnosis, treatment recommendation, or personalised sleep advice will be provided. The expected risks are minimal and may include mild boredom or tiredness, mild discomfort when reflecting on sleep habits or making self-other allocation decisions, minor inconvenience from completing the 7-day diary, and privacy concerns about sleep schedule information. Risk will be minimised through informed consent, voluntary participation, the right to withdraw, non-clinical wording, pseudonymisation, separate storage of identifiable records, and restricted access to research data.

Tipo di studio

Osservativo

Iscrizione (Stimato)

128

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Backup dei contatti dello studio

Luoghi di studio

    • Kowloon
      • Hung Hom, Kowloon, Hong Kong
        • The Hong Kong Polytechnic University
        • Contatto:
        • Contatto:
        • Sub-investigatore:
          • Bryant HUI, PhD

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

Metodo di campionamento

Campione non probabilistico

Popolazione di studio

Adults aged 18 years or above will be recruited as healthy volunteers from university and community settings. Eligible participants may include university students, university staff, and community adults who can understand English or Chinese study materials and complete computer-based behavioural tasks, sleep-related questionnaires, and a 7-day sleep diary. The study is not limited to PolyU students and is not designed to recruit participants with any specific sleep disorder, mental health condition, or clinical diagnosis.

Descrizione

Inclusion Criteria:

  • Aged 18 years or above.
  • Able to provide informed consent.
  • Able to understand English or Chinese study materials.
  • Able to complete computer-based behavioural tasks and self-report questionnaires.
  • Willing to complete a 7-day sleep diary.

Exclusion Criteria:

  • Aged under 18 years.
  • Unable to provide informed consent.
  • Unable to complete study materials in English or Chinese.
  • Prior participation in the same study.
  • Self-reported condition or circumstance that would make participation in a brief computer-based decision-making task or sleep-related questionnaires inappropriate or distressing.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

Coorti e interventi

Gruppo / Coorte
Intervento / Trattamento
Adult Participants
Adults aged 18 years or above who provide informed consent and complete sleep-related self-report measures, a 7-day sleep diary, and a computer-based prosocial allocation task. Participants are not assigned to any sleep manipulation, treatment, or intervention. Sleep quality, sleep timing, chronotype, and prosocial allocation behaviour are measured as naturally occurring individual differences.
Participants complete non-diagnostic sleep and circadian self-report measures, including the Pittsburgh Sleep Quality Index, the Munich Chronotype Questionnaire, and a 7-day sleep diary, followed by a brief computer-based Dictator Game allocation task. This is an observational assessment procedure only. Participants are not assigned to a treatment, sleep manipulation, sleep deprivation, sleep restriction, or behaviour-change intervention.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Dictator Game Prosocial Allocation Score
Lasso di tempo: Day 1 (single study session)
Prosocial allocation behaviour will be measured using a brief computer-based Dictator Game task. The primary behavioural score will be the number or proportion of trials in which the participant selects the more prosocial allocation option across the task, with higher scores indicating more prosocial allocation choices.
Day 1 (single study session)

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Pittsburgh Sleep Quality Index Global Score
Lasso di tempo: Day 1 (single study session)
Subjective sleep quality over the previous month will be assessed using the Pittsburgh Sleep Quality Index (PSQI). The PSQI global score is calculated according to standard scoring procedures and ranges from 0 to 21, with higher scores indicating poorer subjective sleep quality. The PSQI is used as a non-diagnostic research measure.
Day 1 (single study session)
Chronotype (Sleep-Corrected Mid-Sleep on Free Days, MSFsc) From the Munich Chronotype Questionnaire
Lasso di tempo: Day 1 (single study session)
Circadian preference (chronotype) will be assessed using the Munich Chronotype Questionnaire (MCTQ). The chronotype variable reported is the sleep-corrected mid-sleep time on free days (MSFsc), expressed as clock time in decimal hours, with later values indicating a later (more evening) chronotype. The MCTQ is used as a non-diagnostic research measure.
Day 1 (single study session)
Mean Sleep Duration From the 7-Day Sleep Diary
Lasso di tempo: Daily for the 7 days before the study session (Days -7 to -1)
Nightly sleep duration will be recorded in a 7-day sleep diary and averaged across the diary days to yield mean sleep duration, reported in hours per night.
Daily for the 7 days before the study session (Days -7 to -1)

Altre misure di risultato

Misura del risultato
Misura Descrizione
Lasso di tempo
Dictator Game Response Time
Lasso di tempo: Day 1 (single study session)
Response time for Dictator Game allocation choices may be recorded as an exploratory behavioural measure, where available. Response time will not be interpreted as a clinical measure.
Day 1 (single study session)

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Pubblicazioni e link utili

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Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

1 luglio 2026

Completamento primario (Stimato)

1 giugno 2028

Completamento dello studio (Stimato)

1 giugno 2028

Date di iscrizione allo studio

Primo inviato

30 giugno 2026

Primo inviato che soddisfa i criteri di controllo qualità

6 luglio 2026

Primo Inserito (Effettivo)

13 luglio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

13 luglio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

6 luglio 2026

Ultimo verificato

1 giugno 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Descrizione del piano IPD

Individual participant data will not be shared outside the approved research team. Study findings will be reported in aggregate form only. Pseudonymised or anonymised data may be retained for future ethically approved research only if permitted by participant consent and institutional ethics approval.

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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