Skip to content

Vitoria Sleep Smart City: Interactive Intervention for Sleep Improvement

Vitoria Sleep Smart City: Interactive Intervention for Sleep Improvement.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05066581
Acronym
SMARTCITY
Enrollment
202
Registered
2021-10-04
Start date
2021-06-21
Completion date
2022-11-30
Last updated
2023-04-03

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

Conditions

Sleep Deprivation, Sleep Hygiene

Brief summary

Currently, the investigators know that there is a high and increasing prevalence of sleep quality and quantity deficits in the general population with the social and health consequences that this entails. There are numerous activity wristbands linked to mobile apps that analyze sleep, but none can generate individualized recommendations for improvement interacting with the person. The main objective of the current project is to develop a virtual and interactive sleep assistant to increase the quantity and quality of sleep. Secondary objectives being the improvement of daytime sleepiness and the quality of life of the persons. Methodology: 202 participants in active employment who meet the criteria of poor sleepers (defined by a Pittsburg test score \>5) are divided into 2 study groups. 1. Intervention group: Sleep data will be collected using validated questionnaires (SATED and the Sleep Hygiene Index) and objectively employing an activity bracelet, in which weekly, through a live chat, the medical staff of the sleep units will offer recommendations for the improvement of the deficits detected. 2. Control group: Same protocol as the intervention group, but the participants will not receive the recommendations via the interactive chat.

Interventions

DEVICELive Chat

Subjects from the intervention group will be able to ask for a medical intervention if needed with the phisycians from the sleep unit. After the following period, we expect to see better sleep habits in this group when compared to the no intervention one

Sponsors

Philips Healthcare
CollaboratorINDUSTRY
Ayuntamiento de Vitoria
CollaboratorUNKNOWN
Ibermatica
CollaboratorUNKNOWN
Bioaraba
CollaboratorUNKNOWN
Hospital Universitario Araba
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SCREENING
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Patients aged 18 to 65 years

Exclusion criteria

* Patients previously diagnosed and treated for sleep pathology (such as insomnia, Obstructive Sleep Apnea (OSA), Restless Legs Syndrome (RLS), narcolepsy or parasomnia, among others). * Severe medical or psychiatric comorbidities. * Subjects who are not capable of using mobile technology such as Smartphone. * Subjects who are not committed to actively participate, putting into practice the sleep recommendations given by the assistant.

Design outcomes

Primary

MeasureTime frameDescription
Total sleep timeEight monthsBy measuring total sleep time, determine the objective of sleeping between 7 and 9 hours per day on average.

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026