Physical Activity Level in Patients With OSAS During Covid-19 Pandemic

Sponsor
Ahi Evren Chest and Cardiovascular Surgery Education and Research Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT04451993
Collaborator
(none)
63
1
3.2
19.8

Study Details

Study Description

Brief Summary

As long as the people stay at home because of the Covid 19 outbreak, the investigators assume that the sleep quality of OUAS patients, like everyone else, and the sleep quality of COVID-19 outbreak are reduced due to anxiety and anxiety in people. In addition, we assume that sleep quality and physical activity level are related to health literacy level and fear of movement (kinesiophobia). In this study; the investigators aimed to determine how patients are affected by this process by evaluating sleep quality, physical activity, fear of movement and health literacy in OSAS patients during our stay in the COVID-19 outbreak.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Research Ahi Evren Chest Cardiovascular Surgery Training Research Hospital will be performed in patients between the ages of 18-70 years, diagnosed with OSAS in the sleep laboratory. Sleep quality, physical activity, fear of movement and health literacy will be evaluated in OSAS patients. Evaluations will be made by phone In order for the study to be strong, it will be tried to reach the maximum patient that can be taken between June 2020 and October 2020.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    63 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Prospective
    Official Title:
    Are the Sleep Quality and Physical Activity Levels of Osas Patients Differently From Healthy People During the COVID-19 Pandemic:a Prospective, Descriptive Study
    Actual Study Start Date :
    Jun 25, 2020
    Actual Primary Completion Date :
    Sep 1, 2020
    Actual Study Completion Date :
    Sep 30, 2020

    Arms and Interventions

    Arm Intervention/Treatment
    OSAS PATIENTS

    mild, moderate and severe OSAS patients

    HEALTHY INDIVIDUALS

    healthy individuals without chronic disease

    Outcome Measures

    Primary Outcome Measures

    1. Physical Activity [1 day]

      International Physical Activity Questionnaire/ In activity-specific scoring, walking under the heading of the fields is calculated by the sum of the moderate intensity activity and intensive activity in itself. From these calculations, a score is obtained in MET-minutes. There are 3 categories of physical activity level classification. Physical activity levels are classified as physically inactive (inactive), low level of physical activity (minimally active) and sufficient level of physical activity (very active)

    2. Sleep Quality [1 day]

      The Pittsburgh Sleep Quality Index

    Secondary Outcome Measures

    1. Daytime Sleepiness [1 day]

      In order to measure the general sleepiness of people during the day, it was evaluated with a standard questionnaire, which is defined as Epworth sleepiness scale (EUS) and consists of 8 questions. The answers for each question are scored between 0 and 3 and the total score is obtained. The score obtained above 10 in EUS has high sensitivity and specificity for daytime sleepiness.

    2. Fear of movement [1 day]

      Tampa Kinesiophobia Scale (TKS)The person gets a total score between 17-68. The high score on the scale indicates that kinesiophobia is also high

    3. Health literacy [1 day]

      Translated into Turkish TURKEY health literacy SCALE-32 (Tsoy-32) will be used. It was used to evaluate the literacy rates of individuals over the age of 15. 0 indicates the lowest health literacy and 50 indicates the highest health literacy.

    Other Outcome Measures

    1. Circadian rhythm evaluation [1 day]

      In the human circadian rhythm, the Morning Morning-Evening Survey (SAA) form was used, which determined morning and evening types.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    19 Years to 70 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    1. Having been diagnosed with OSAS and disease severity determined,

    2. Being between the age of 19-70,

    3. Body mass index <40 kg / m2

    4. Volunteering to participate in the research,

    5. Not having a mental problem that will hinder the cooperation.

    Exclusion Criteria:
    1. To have advanced orthopedic, neurological and cardiovascular disease,

    2. Having a cognitive problem,

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Trabzon Ahi Evren Thoracic and Cardiovascular Surgery Training and Research Hospital Trabzon Turkey

    Sponsors and Collaborators

    • Ahi Evren Chest and Cardiovascular Surgery Education and Research Hospital

    Investigators

    • Study Director: Naciye Vardar-Yagli, PhD, Hacettepe University
    • Study Chair: Adem Celik, MD, Ahi Evren Chest, Heart and Vascular Surgery Training and Research Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    NUREL ERTURK, Phd student, Ahi Evren Chest and Cardiovascular Surgery Education and Research Hospital
    ClinicalTrials.gov Identifier:
    NCT04451993
    Other Study ID Numbers:
    • GO 20/540
    First Posted:
    Jun 30, 2020
    Last Update Posted:
    Feb 5, 2021
    Last Verified:
    Feb 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by NUREL ERTURK, Phd student, Ahi Evren Chest and Cardiovascular Surgery Education and Research Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 5, 2021