- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04346953
Video-Based Exercise for Individuals With Social Isolation Due to Coronavirus (COVID-19)
Investigation Of The Effectiveness Of Video-Based Exercise Program Applied To Adult Individuals Who Experience Social Isolation At Houses Due To The Coronavirus (COVID-19) Pandemic
In December 2019, new coronavirus pneumonia (COVID-19) broke out in Wuhan (Hubei, China), and it spread rapidly from one city to the whole country in just 30 days, and then worldwide cases began to appear. All the countries of the world take some precautions to prevent the spread of this epidemic disease, which WHO declared as "pandemic". Apart from compulsory situations, non-home and social isolation are the primary measures. However, not leaving the house and social isolation brings with it the restriction of physical activity.
According to World Health Organization (WHO), in order to obtain health benefits, adult individuals between the ages of 18-64 should perform at least 150 minutes of physical activity per week (30 minutes a day for 5 days a week) or intensive physical activity for at least 75 minutes a week. For additional health benefits, adults should increase their moderate-intensity physical activities to at least 300 minutes a week or equivalent. Physical activity; It is directly related to the prevention of chronic diseases, increasing fitness, strengthening the muscles and increasing the quality of life. It is reported that one of the ten main risk factors in terms of mortality in the world is insufficient physical activity. The effects of social isolation are related to physical inactivity, smoking and the possibility of having both health risk behaviors together. Practical and innovative interventions are needed to reduce physical performance and decrease in muscle mass, strength and physical performance in the aging population. Considering today's conditions and current COVID-19 Pandemic, technology-supported exercise programs are effective in increasing the motivation for physical activity. The purpose of this study; In order to prevent the spread of the COVID-19 pandemic, social isolation, which is one of the measures taken in our country, is to evaluate the physical activity level of adults and to investigate the effectiveness of home exercises. It is aimed to use a model based on the video supported by a home-based exercise program.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Istanbul, Turkey
- Istinye University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Being between 40-60 years old
- Being in social isolation due to COVID-19 virus
- Not having any physical disability that prevents them from doing physical activities
- Being in social isolation due to COVID-19 virus
- Having access to exercise videos
Exclusion Criteria:
- Having a serious cognitive impairment
- Having serious hearing and vision problems
- Having vestibular disorders that can cause loss of balance
- Having diabetes and/or hypertension or a neurological disease
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Study Group
The group to which the exercise videos consisting of aerobic and strengthening exercises will be applied.
|
Individuals (n = 64) to be included in the study group will be grouped according to the levels of physical activity (low, medium, high level) determined by the International Physical Activity Questionnaire.
An exercise program will be created for each group based on physical activity levels and videos of these exercise programs will be prepared.
The videos will be scheduled for 20 minutes.
Individuals will be asked to apply for these programs with video for 20 minutes every day for 6 weeks.
Exercise programs will start with pulmonary exercises and warm-up exercises to prepare for exercise.
The exercise program will end with cool down exercises.
The exercise protocol will be determined as a combination of aerobic and strengthening exercises.
|
|
No Intervention: Control Group
The control group where only the evaluations will be made and information about the benefits of exercise will be given.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Nottingham Health Profile
Time Frame: 2 weeks
|
Nottingham Health Profile was created in England in 1985 to evaluate the quality of life-related to health.
The Nottingham Health Profile is a general quality of life questionnaire that assesses the level of individuals health problems and how they affect their daily life activities.
|
2 weeks
|
|
International Physical Activity Questionnaire - Short Form
Time Frame: 2 weeks
|
The International Physical Activity Questionnaire -Short Form (IPAQ-SF) measures the frequency and duration of moderate physical activity, vigorous physical activity, walking, and sedentary behavior using 7 questions and is considered more suitable for population surveillance and large-scale studies compared with the long form .
The IPAQ-SF was validated for adults.According to the score obtained, the physical activity levels of individuals are determined.
It indicates lower physical activity level below 600 Metabolic Equivalent Threshold (MET)-min per week, medium physical activity level between 600-3000 Metabolic Equivalent Threshold (MET)-min per week and high physical activity level between 600-3000 Metabolic Equivalent Threshold (MET)-min per week.
|
2 weeks
|
|
Beck Depression Inventory
Time Frame: 2 weeks.
|
It is among the most used scales to measure depression all over the world.
It consists of 21 questions in total.
Each item gets points between 0-3.
11-17 points indicate mild depression, 18-29 points indicate moderate depression, and 30-63 points indicate severe depression.
|
2 weeks.
|
|
Beck Anxiety Inventory
Time Frame: 2 weeks
|
It is used to evaluate the anxiety symptoms experienced by individuals due to social isolation.
It consists of 21 items and is scored between 0-3.
It indicates low anxiety of 0-21 points, moderate anxiety of 22-35 points and high anxiety of 36 points and above.
|
2 weeks
|
|
Pittsburgh Sleep Quality Index
Time Frame: 2 weeks
|
It is a scale that provides information about sleep quality and type and severity of sleep disorder in the last month.
The sleep quality of the person on this scale; sleep latency, sleep duration, habitual sleep efficiency, sleep disturbance, sleep medication use and daytime dysfunction.
Each question is given a score of 0-3.
High scores reflect poor sleep quality.
If the total score obtained from the scale is less than 5, it is defined as "Good sleep quality" and 5 and above is defined as "Bad sleep quality".
|
2 weeks
|
|
Timed Get Up and Go Test
Time Frame: 2 weeks
|
Used for mobility assessment.
The test begins while the person is sitting in the chair.
The person is asked to get up from the chair, walk 3 meters, come back and sit on the chair again, and the time is recorded.
If an elderly person completes the test for more than 12 seconds, there is a risk of falling.
|
2 weeks
|
|
Flamingo Balance Test
Time Frame: 2 weeks
|
Flamingo Balance Test will be used to evaluate the static balance of the individuals who will participate in the study.
This test is done on one foot.
While individuals are in balance with one foot, time begins and tries to stay in balance for 1 minute.
The time is stopped when the balance is disturbed.
When the time is completed, each individual attempt to balance is counted and this number is recorded as the individual's score at the end of the test.
If the individual tries to balance 15 times in the first 30 seconds, the test is stopped and zero points are given.
|
2 weeks
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 002 (University of CT Health Center)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Healthy Lifestyle
-
Eindhoven University of TechnologyCompletedLifestyle | Lifestyle, Healthy | Lifestyle Risk Reduction | Lifestyle, SedentaryBelgium
-
Buchinger Wilhelmi Development & Holding GmbHKing's College London; Buchinger Wilhelmi Clinic; MVZ Labor Ravensburg GbR; Synlab...CompletedHealthy Lifestyle | Healthy NutritionGermany
-
Mälardalen UniversitySwedish Environmental Research Institute (IVL)Active, not recruitingHealthy Diet | Healthy LifestyleSweden
-
Prevent Age Resort "Pervaya Liniya"RecruitingHealthy Aging | Healthy Diet | Healthy LifestyleRussian Federation
-
Assaf-Harofeh Medical CenterRecruiting
-
State University of LondrinaCompletedHealthy LifestyleBrazil
-
University of Southern CaliforniaNational Institute on Aging (NIA)CompletedHealthy LifestyleUnited States
-
South Dakota State UniversityActive, not recruiting
-
University of Southern CaliforniaAntelope Valley Partners for Health; Wesley Health Centers - Antelope ValleyCompleted
-
Örebro University, SwedenRecruiting
Clinical Trials on Video based exercise
-
Tarsus UniversityThe Scientific and Technological Research Council of TurkeyRecruitingAmyotrophic Lateral SclerosisTurkey (Türkiye)
-
Istanbul Medipol University HospitalCompleted
-
Acibadem UniversityCompleted
-
Istanbul Medipol University HospitalCompletedParkinson Disease | Exercise | Therapy | ExergameTurkey (Türkiye)
-
Istanbul Galata UniversityActive, not recruiting
-
Ilke KARACompletedMuskuloskeletal DiseasesTurkey
-
Biruni UniversityIstanbul University - Cerrahpasa (IUC)CompletedPhysical Inactivity | Social Isolation | Well-BeingTurkey
-
Uludag UniversityNot yet recruitingPain Management | Breathing Exercise | Non-Pharmacological Interventions | Venipuncture Pain
-
Anne KloosCompletedHuntington's DiseaseUnited States
-
Serra SürelCompletedExercise Therapy | Non Specific Chronic Low Back PainTurkey