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Sleep & Quality of Life Evaluation of Patients With Atopic Dermatitis Based on E-diary on a Smartphone Application and Actigraphy

Sleep & Quality of Life Evaluation of Patients With Atopic Dermatitis Based on Real-world Data Collection With a Smartphone Application and a Validated Actigraphy Wristband

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03090178
Acronym
ACTISLEEP
Enrollment
52
Registered
2017-03-24
Start date
2017-06-02
Completion date
2018-06-15
Last updated
2018-08-08

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

Conditions

Atopic Dermatitis Eczema

Brief summary

Atopic dermatitis is a chronic disease with a high impact on patient's quality of life. Nocturnal pruritus is one of the main symptoms affecting quality of life. Treatment efficacy is generally measured by healthcare professionals during consultations with both questioning and visual examination of the lesions. Quality of Life (QoL) can also be evaluated retrospectively with the Dermatology Life Quality Index (DLQI) scale. Collecting data retrospectively introduces a significant recall bias that can be addressed by collecting data in Real World (RW). Real World data collection is prospective and take place within the patient's own environment. While data collection is generally done with diaries, it has been demonstrated that smartphone and connected devices were able to produce more precise and granular data than traditional methods.

Detailed description

The main objective of the study is to demonstrate a medical hypothesis using a wristband actigraph: patients with moderate to severe atopic dermatitis have a poorer quality and quantity of sleep than healthy subject. Secondary objetives are to assess the interest of a smartphone application in evaluating the quality of life of patients with moderate to severe atopic dermatitis in regard of those of healthy volunteers.

Interventions

OTHERelectronic-Patient Report Outcome and wear of a wristband actigraph

Measurement of sleep quality and quantity with wristband actigraph and evaluation of quality of life with electronic-Patient Report Outcome

Sponsors

Ad scientiam
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
OTHER
Masking
NONE

Intervention model description

Investigators will first enroll patients, then healthy volunters. Healthy volunters will be matched to patients on age, sexe and wake up at a programmed time

Eligibility

Sex/Gender
ALL
Age
18 Years to 120 Years
Healthy volunteers
Yes

Inclusion criteria

Patients : * Subjects using a smartphone running Apple operating system (iOS 7 and above) or Android (version 2.2 and above) * Subjects agreeing to wear the actigraphy wristband at night * Subjects 18 years old or older * Subjects affiliated to French Health Insurance * Subjects treated for moderate to severe atopic dermatitis or atopic dermatitis exacerbation\* \*The stage of the atopic dermatitis will be assessed by using the Eczema Area and Severity Index (EASI), Body Surface Area (BSA) and Investigator Global Assessment (IGA). The EASI is an investigator-assessed instrument measuring the severity of clinical signs in atopic dermatitis. The EASI was identified as one of the best-validated outcome measures for atopic dermatitis. A moderate to severe atopic dermatitis corresponds to: * Eczema Area and Severity Index score ≥ 7.1 * Investigator Global Assessment ≥ 3 * Body Surface Area ≥ 10 Healthy volunters : * Subjects using a smartphone running iOS (iOS 7 and above) or Android (version 2.2 and above) * Subjects agreeing to wear the actigraphy wristband at night * Subjects 18 years old or older * Subjects affiliated to French Health Insurance * Subjects without a dermatology disease Non inclusion Criteria: * -Illiterate subjects * Subjects not proficient in French * Subject with a primary insomnia\* \*Insomnia, sleep apnea and hypersomnia will be evaluated with respectively 3 tests: * Insomnia Severity Index (ISI); * Berlin Sleep Apnea Scale; * Epworth Scale * Subjects treated by hypnotic drugs * Pregnant woman * Subjects under guardianship

Exclusion criteria

If a participant is taking hypnotic treatments during his study participation, he will be excluded from the clinical trial.

Design outcomes

Primary

MeasureTime frameDescription
Sleep quality15 daysMeasure of sleep quality

Secondary

MeasureTime frameDescription
Sleep quantity15 daysMeasure of sleep quantity

Other

MeasureTime frameDescription
Quality of lifetwo times a day for 15 dayselectronic patient report outcome on a secured mobile application

Countries

France

Outcome results

None listed

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