Chilipad Sleep Optimization Study
ConditionSleep
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorEfforia, Inc
About this trial
This study evaluates the Chilipad Dock Pro Bed Cooling System and Sleep Tracker, examining how bed temperature influences sleep quality and overall well-being.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Can read and understand English.
US resident.
Willing and able to follow the requirements of the protocol.
Disqualifiers
Individuals with concerns about water leakage.
Individuals with sleep disorders related to changes in temperature
Individuals with thermal sensitivity
Individuals who are easily frustrated by technology.
Trial design
Design model
Single group
Treatments tested in this trial
Chilipad Dock Pro Bed Cooling System and Sleep Tracker
DeviceThe Chilipad Dock Pro Bundle is an advanced sleep system designed to optimize sleep by dynamically adjusting the bed's surface temperature. It consists of a thermoregulated mattress pad and a Dock Pro control unit that actively circulates water through the pad, allowing users to customize the temperature between 55°F and 115°F. The system offers both single and dual control, making it ideal for individual or shared use. Equipped with AI-driven features, the Dock Pro can monitor sleep patterns and environmental factors to make real-time adjustments, ensuring optimal sleep conditions throughout the night. This intelligent temperature management system is only enhanced when paired with the optional Sleepme Tracker, creating a personalized sleep experience.
Treatment groups
100 Participants
are divided into 1 treatment groupGroup A: Single arm where participants act as their own controlExperimental treatment 1 intervention
Trial outcomes
Primary outcomes
1
PROMIS Sleep Disturbance Scale
The PROMIS Sleep Disturbance Scale is a validated and widely used assessment tool developed as part of the Patient-Reported Outcomes Measurement Information System (PROMIS) initiative. It is designed to measure the severity of sleep disturbances and disruptions experienced by individuals. This scale includes a range of questions that assess the frequency and impact of various sleep-related issues, such as difficulty falling asleep, nighttime awakenings, and restless sleep. Healthcare professionals and researchers rely on this scale to better understand and quantify sleep problems in patients, enabling them to tailor interventions and treatment strategies to address sleep-related concerns effectively.
Time frame
Change from baseline (Day 1-3) in PROMIS Sleep Disturbance Scale at 4 weeks after the start of the intervention (Day 27-33)2
Well-being Survey
Please answer the following questions to assess your well-being.
Time frame
Change from baseline (Day 1-3) in Well-being Survey at 4 weeks after the start of the intervention (Day 27-33)3
36-Item Short Form Survey Instrument (SF-36)
The SF-36, or Short Form 36, is a widely used health-related quality of life questionnaire that consists of 36 questions designed to assess a person's physical and mental well-being. It measures various aspects of an individual's health, including physical functioning, role limitations due to physical and emotional problems, social functioning, mental health, energy and vitality, pain, and general health perceptions. The SF-36 provides a comprehensive overview of a person's health status and is frequently used in clinical research, healthcare assessments, and population health studies. Its versatility and ability to assess multiple dimensions of health make it a valuable tool for evaluating the impact of medical interventions and health-related interventions.
Time frame
Change from baseline (Day 1) in SF-36 at 4 weeks after the start of the intervention (Day 29-31)Sponsors and contacts
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Source ClinicalTrials.gov