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Smart Sleep In-home Validation Extension Study

Primary Purpose

Healthy, Sleep Deprivation, Insufficient Sleep Syndrome

Status

Completed

Phase

Not Applicable

Locations

United States

Study Type

Interventional

Intervention

SmartSleep Boost On

SmartSleep Boost Off

About this trial

This is an interventional treatment trial for Healthy

Eligibility Criteria

21 Years - 50 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Able to provide informed consent
Live in the US
Able to read, write and speak English
Adult volunteers aged 21-50
Smartphone owner (iOS 9+ or Android 5.0+ OS)
Access to home Wi-Fi for syncing of SmartSleep data and cognitive testing
Working full time schedule [Note: Full time is considered a 32 hour work week start time at 7am or later]
Suffer from short sleep due to lifestyle
- Gets less than 7 hours of sleep at least 3 days a week (via self-report)
- Get at least 5 hours of sleep per night 7 nights a week (via self-report)
- Gets 1 extra hour of sleep on the weekends (via self-report of extended nightly sleep or daytime nap)

Exclusion Criteria:

Individuals who self-report severe contact dermatitis or an allergy to silver
Diagnosed as having any of the following conditions (via self-report):
- Sleep Apnea
- Insomnia
- Restless legs syndrome
- Parasomnia
- Epilepsy/Seizures
Diagnosed as having any major organ system disease such as congestive heart failure, neuromuscular disease, renal failure, cancer, chronic obstructive pulmonary disease, respiratory failure or respiratory insufficiency, or patients requiring oxygen therapy (via self-report)
High Risk of Obstructive Sleep Apnea (OSA) based on Questionnaire
Daily caffeine intake > 650 mg
History of moderate hearing loss (via self-report)
Currently working night shift or rotating shift
Head circumference <54 cm (21 in) or >66 cm (26 in)
Individuals who self-report taking longer than 30 minutes more than 3 times a week to fall asleep once they turn lights off
Individuals who self-report regularly taking sleeping pills (more than once per week), including prescription or over the counter (OTC) pills such as Ambien, Tylenol PM or Zzzquil
Pregnant (via self-report)
Employee of Philips or spouse of a Philips employee
Employee (or spouse of an employee) of a company that designs, sells, or manufactures sleep-related products
Not able to comply with study procedures

Sites / Locations

Florida Lung & Sleep Associates

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Active Comparator

Arm Label

SmartSleep Boost Off

SmartSleep Boost On

Arm Description

Participants wear the device for baseline data collection in boost off mode. There is no intervention. This is known as SmartSleep Boost Off mode.

Participants wear the device for 3 weeks in boost on mode. This is known as SmartSleep Boost On mode.

Outcomes

Primary Outcome Measures

The effects of the auditory stimulation delivered by the SmartSleep device in adults with shortened sleep schedules due to lifestyle as determined by changes in the cumulative (CSWA) or average slow-wave activity.

Efficacy will be evaluated based on the average of seven nights of use collecting baseline data compared to the average of twenty one nights of active SmartSleep, while in the home setting. SWA accumulation over Non-Rapid Eye Movement (NREM) sleep (CSWA) will be analyzed for each night in the active condition using as reference the average CSWA across baseline nights.

Secondary Outcome Measures

Change in performance of the Matrix reasoning task (MRT) correlated to the changes in CSWA over the trial period.

Performance of the MRT during baseline and active use weeks of the SmartSleep Device will be compared to changes in CSWA over the trial period.

Change in performance of the Digital Symbol Substitution Task (DSST) correlated to the changes in CSWA over the trial period.

Performance of the DSST during baseline and active use weeks of the SmartSleep Device will be compared to changes in CSWA over the trial period.

Change in performance of the Psychomotor Vigilance Testing -Brief (PVT) correlated to the changes in CSWA over the trial period.

Performance of the PVT during baseline and active use weeks of the SmartSleep Device will be compared to changes in CSWA over the trial period.

Change in sleepiness/alertness as measured by a 7 point scale correlated to the changes in CSWA over the trial period.

Change in sleepiness/alertness as measured by a 7 point scale during baseline and active use weeks of the SmartSleep Device will be compared to changes in CSWA over the trial period.

Full Information

NCT ID

NCT03665844

First Posted

September 5, 2018

Last Updated

November 15, 2018

Sponsor

Philips Respironics

1. Study Identification

Unique Protocol Identification Number

NCT03665844

Brief Title

Smart Sleep In-home Validation Extension Study

Official Title

Smart Sleep In-home Validation Extension Study

Study Type

Interventional

2. Study Status

Record Verification Date

November 2018

Overall Recruitment Status

Completed

Study Start Date

August 14, 2018 (Actual)

Primary Completion Date

November 7, 2018 (Actual)

Study Completion Date

November 7, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title

Sponsor

Name of the Sponsor

Philips Respironics

4. Oversight

Studies a U.S. FDA-regulated Drug Product

Studies a U.S. FDA-regulated Device Product

Data Monitoring Committee

5. Study Description

Brief Summary

This study is a nonrandomized, unblinded, uncontrolled case series clinical trial validating the SmartSleep product, including SleepMapper app in the home setting. It is intended to provide data related to product use and cognitive testing incorporating a longer baseline period for comparison purposes. It will include adults (21-50 yr. old) who are working full time and report shortened sleep due to lifestyle. For the purposes of this study, shortened sleep is defined as sleeping at least 5 hrs. of sleep per night, and sleeping less than or equal to 7 hrs. at least 3 nights per week. Participants also increase their sleep duration by ≥ 1 hour on the weekends. In addition, participants report a sleep latency ≤ 30 minutes less than or equal to 3 nights per week. Participants are generally healthy individuals who have not been diagnosed with any sleep-related medical conditions. In addition, participants diagnosed with major organ system diseases or requiring oxygen therapy are excluded from participation. Up to 75 individuals will be consented in order to complete a total of 50 participants using a nonrandomized design. The study involves an initial screening visit followed by home use of the SmartSleep device with SleepMapper app. The home use will include an initial week of baseline use followed by 3 weeks of use with boost on. Study staff will contact participants after the first week of use as a reminder. Participants will be asked to complete a battery of cognitive tests upon wake up each morning. Participants will be asked to complete a question twice daily during the home use period. Additional phone calls may occur on an as needed basis if issues arise. The final visit will be an in facility visit in which all study equipment will be returned. The anticipated study duration will be up to 6 weeks (including the 4 weeks of use period).

Detailed Description

Study procedures Visit 1 (Screening) Procedures (up to 2 hours): Participants will be asked to report to the research site for a daytime visit. A detailed interview will be performed verifying eligibility criteria, as well as a review of work and non-work schedules. After a full explanation of the protocol and after all the participants' questions have been answered, they will be asked to sign the consent form. Participants will complete the following baseline information: Demographics Questionnaires Medical History Questionnaire Review of Current Medications Height, Weight, Head Measurements Cognitive Assessment training Once eligibility confirmed, participants will be trained in the use of the SmartSleep device, including pairing and syncing of the SleepMapper app Home Use (weeks 1-4) All participants will be asked to wear the device consecutively every night. The anticipated study participation is expected to be one month of use (+ 2 weeks based on participant schedule). All participants will wear the device for 1 week of baseline use. Post one week of use (+/- 2 days), participants will the active mode. Participants will continue nightly home use of the SmartSleep with boost enabled for the next 3 weeks. Participants will be asked to complete the cognitive testing daily after wake up. Cognitive tests should be performed at the same time each morning following the same routine. Participants will be asked to complete the a question twice daily. During the study if a participant's medical history or medication changes, they will be asked to inform the study team. Participants will be asked during the course of the study if they experience any discomfort, red marks, etc. Study completion (final visit) Participants will be asked to return to the lab for a final study visit. They will be asked to bring their study materials.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study

Healthy, Sleep Deprivation, Insufficient Sleep Syndrome

7. Study Design

Primary Purpose

Treatment

Study Phase

Not Applicable

Interventional Study Model

Crossover Assignment

Model Description

1 week baseline, 3 weeks active condition

Masking

None (Open Label)

Allocation

Non-Randomized

Enrollment

61 (Actual)

8. Arms, Groups, and Interventions

Arm Title

SmartSleep Boost Off

Arm Type

Placebo Comparator

Arm Description

Participants wear the device for baseline data collection in boost off mode. There is no intervention. This is known as SmartSleep Boost Off mode.

Arm Title

SmartSleep Boost On

Arm Type

Active Comparator

Arm Description

Participants wear the device for 3 weeks in boost on mode. This is known as SmartSleep Boost On mode.

Intervention Type

Device

Intervention Name(s)

SmartSleep Boost On

Intervention Description

SmartSleep device can be configured to two different settings. SmartSleep Boost On setting provides soft audio tones during the night. It's a non-invasive portable light weight device designed to stimulate deep slow wave sleep (SWS).

Intervention Type

Device

Intervention Name(s)

SmartSleep Boost Off

Intervention Description

SmartSleep device can be configured to two different settings. SmartSleep Boost Off provides no audio tones.

Primary Outcome Measure Information:

Title

Description

Time Frame

4 weeks

Secondary Outcome Measure Information:

Title

Change in performance of the Matrix reasoning task (MRT) correlated to the changes in CSWA over the trial period.

Description

Performance of the MRT during baseline and active use weeks of the SmartSleep Device will be compared to changes in CSWA over the trial period.

Time Frame

4 weeks

Title

Change in performance of the Digital Symbol Substitution Task (DSST) correlated to the changes in CSWA over the trial period.

Description

Performance of the DSST during baseline and active use weeks of the SmartSleep Device will be compared to changes in CSWA over the trial period.

Time Frame

4 weeks

Title

Change in performance of the Psychomotor Vigilance Testing -Brief (PVT) correlated to the changes in CSWA over the trial period.

Description

Performance of the PVT during baseline and active use weeks of the SmartSleep Device will be compared to changes in CSWA over the trial period.

Time Frame

4 weeks

Title

Change in sleepiness/alertness as measured by a 7 point scale correlated to the changes in CSWA over the trial period.

Description

Change in sleepiness/alertness as measured by a 7 point scale during baseline and active use weeks of the SmartSleep Device will be compared to changes in CSWA over the trial period.

Time Frame

4 weeks

10. Eligibility

Sex

All

Minimum Age & Unit of Time

21 Years

Maximum Age & Unit of Time

50 Years

Accepts Healthy Volunteers

Eligibility Criteria

Inclusion Criteria: Able to provide informed consent Live in the US Able to read, write and speak English Adult volunteers aged 21-50 Smartphone owner (iOS 9+ or Android 5.0+ OS) Access to home Wi-Fi for syncing of SmartSleep data and cognitive testing Working full time schedule [Note: Full time is considered a 32 hour work week start time at 7am or later] Suffer from short sleep due to lifestyle Gets less than 7 hours of sleep at least 3 days a week (via self-report) Get at least 5 hours of sleep per night 7 nights a week (via self-report) Gets 1 extra hour of sleep on the weekends (via self-report of extended nightly sleep or daytime nap) Exclusion Criteria: Individuals who self-report severe contact dermatitis or an allergy to silver Diagnosed as having any of the following conditions (via self-report): Sleep Apnea Insomnia Restless legs syndrome Parasomnia Epilepsy/Seizures Diagnosed as having any major organ system disease such as congestive heart failure, neuromuscular disease, renal failure, cancer, chronic obstructive pulmonary disease, respiratory failure or respiratory insufficiency, or patients requiring oxygen therapy (via self-report) High Risk of Obstructive Sleep Apnea (OSA) based on Questionnaire Daily caffeine intake > 650 mg History of moderate hearing loss (via self-report) Currently working night shift or rotating shift Head circumference <54 cm (21 in) or >66 cm (26 in) Individuals who self-report taking longer than 30 minutes more than 3 times a week to fall asleep once they turn lights off Individuals who self-report regularly taking sleeping pills (more than once per week), including prescription or over the counter (OTC) pills such as Ambien, Tylenol PM or Zzzquil Pregnant (via self-report) Employee of Philips or spouse of a Philips employee Employee (or spouse of an employee) of a company that designs, sells, or manufactures sleep-related products Not able to comply with study procedures

Facility Information:

Facility Name

Florida Lung & Sleep Associates

City

Lehigh Acres

State/Province

Florida

ZIP/Postal Code

33971

Country

United States

12. IPD Sharing Statement

Plan to Share IPD

IPD Sharing Plan Description

No. This data will remain with Florida Lung & Sleep Associates and Philips

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Smart Sleep In-home Validation Extension Study

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