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Citizen Science: The People's Trial: A Randomised Controlled Trial

Citizen Science: The People's Trial: A Randomised Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04185818
Enrollment
500
Registered
2019-12-04
Start date
2019-12-04
Completion date
2020-04-01
Last updated
2020-01-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sleep

Keywords

sleep, book, read, bed

Brief summary

The People's trial is an online pragmatic, randomised controlled trial to determine if reading a book in bed makes a difference to sleep in comparison to not reading a book in bed.

Detailed description

The People's Trial seeks to help enhance the public's understanding of randomised trials by facilitating the involvement of the public in the trial research process. The public have, through an online format, guided the development and design of The People's Trial randomised controlled trial. The People's trial is a parallel, online randomised controlled trial to determine if reading a book in bed makes a difference to sleep in comparison to not reading a book in bed. Members of the public will be recruited through online platforms. Informed consent will be obtained from all participants prior to trial registration. Consent forms will be provided online prior to registration for The People's Trial. Participants will be required to acknowledge that they have read the consent form and give consent to proceed with trail registration. Participants will be randomly allocated into one of two groups: Group 1: Reading a book in bed Group 2: Not reading a book in bed

Interventions

Participants requested to specify usual genre of book they read. 1. Fiction 2. Non-Fiction 3. Other 4. Don't usually read a book in bed

Sponsors

Health Research Board, Ireland
CollaboratorOTHER
National University of Ireland, Galway, Ireland
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Outcomes Assessor)

Intervention model description

The People's Trial is an online pragmatic, randomised controlled trial.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* ≥ 18 years of age on enrollment; * English speaking; * ability to read;

Exclusion criteria

* Members of the public who are unwilling or unable to give informed consent. * Unable to go to bed and wake up at the same time as normal for the study duration. * Unable to sleep in their own bed, in their own home for the study duration * Unable to not eat food or drink caffeinated drinks within 1 hour of bed for the study duration

Design outcomes

Primary

MeasureTime frameDescription
Overall sleep qualityFrom time of randomisation- refers to sleep in the last 7 days onlySleep quality will be measured using the single item sleep quality scale (SQS) (Snyder et al 2018). The SQS is a self-administered questionnaire in which respondents rate overall quality of sleep over a 7-day recall period on a discretizing visual analogue scale from 0 to 10 (0 = terrible, 1-3 = poor, 4-6 = fair, 7-9 = good, and 10 = excellent)

Secondary

MeasureTime frameDescription
Sleep DisturbanceFrom time of randomisation- refers to sleep in the last 7 days onlyThis will be measured using the PROMIS Short Form Sleep Disturbance Scale which measures eight items on 5-point scale to rate the frequency of problems related to insufficient sleep in the past seven days
Daytime sleepinessFrom time of randomisation- refers to sleep in the last 7 days onlyPerceptions of daytime sleepiness will be measured using a a single item with a 10-point scale. Respondents are instructed to indicate their sleepiness at that moment by choosing a number between 1 (not sleepy at all) and 10 (very sleepy). Others have found a single item to measure sleep quality produces reproducible and valid data (Cappelleri, et al 2009, Riegel et al 2013).

Countries

Ireland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 20, 2026