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An Environment for a Better Sleep

Design Beyond Comfort: A Pilot Study on the Critical Role of Ambient Temperature on Sleep Quality and Duration of Occupants in Built environment

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250330065178N1
Enrollment
6
Registered
2025-04-17
Start date
2025-03-30
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Investigation of Sleep Quality Under Different Temperature Conditions. Sleep disorder, unspecified

Interventions

Intervention 1: Intervention Group 1: Participants will sleep in a temperature-controlled room at 18 degrees Celsius, with regulated humidity, darkness, sound, light, and standardized bedding. Their p

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
20 Years to 25 Years

Inclusion criteria

Inclusion criteria: No addiction to drugs or cigarette or alcoholic drinks No Chronic diseases No Sleep disorders with PSQI equal or under 5 scores Healthy BMI Age range of 20 to 25 years, with a maximum standard deviation of 1.5 years

Exclusion criteria

Exclusion criteria: over or under weight addiction to drugs or cigarette or alcoholic drinks Having chronic diseases like high blood pressure Having Sleep disorders or PSQI higher than 5 scores Age outside the age range examined in the study

Design outcomes

Primary

MeasureTime frame
Sleep Efficiency. Timepoint: Physiological parameter measurements are taken at intervals of 10 to 30 seconds. Method of measurement: The device and method for measuring the outcome variable is polysomnography.;Total sleep time. Timepoint: Physiological parameter measurements are taken at intervals of 10 to 30 seconds. Method of measurement: The device and method for measuring the outcome variable is polysomnography.;Slow-wave sleep duration. Timepoint: Physiological parameter measurements are taken at intervals of 10 to 30 seconds. Method of measurement: The device and method for measuring the outcome variable is polysomnography.;Stage durations: N1, N2, N3, REM. Timepoint: Physiological parameter measurements are taken at intervals of 10 to 30 seconds. Method of measurement: The device and method for measuring the outcome variable is polysomnography.;Number of Awakenings. Timepoint: Physiological parameter measurements are taken at intervals of 10 to 30 seconds. Method of measurement: The device and method for measuring the outcome variable is polysomnography.;Subjective Sleep quality. Timepoint: The morning after waking from every test. Method of measurement: 5-Point Likert Scale Questionnaire.;Mean Skin Temperature. Timepoint: Physiological parameter measurements are taken at intervals of 10 to 30 seconds. Method of measurement: Using a medical temperature probe.;Thermal comfort Vote. Timepoint: Before and after each night's test. Method of measurement: 5-Point Likert Scale Questionnaire.;Thermal Sensation Vote. Timepoint: Before and after each night's test. Method of measurement: 7-Point Likert Scale Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHasti Beykpour

Tehran University of Medical Sciences

Hasti.Beyk@edu.ikiu.ac.ir+98 26 3434 9684

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026