Physical Activity During Social Isolation

Social Isolation Clinical Trial

Official title:

What Are the Factors That Affect the Physical Activity Levels of Young Adults During Social Isolation Due to Coronavirus?

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04339491
• Other study ID #: 30042020-1
• Status: Completed
• Start date: April 1, 2020
• Est. completion date: May 31, 2020

Study information

• Verified date: December 2020
• Source: Istanbul University-Cerrahpasa
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The aim of the study is to evaluate the physical activity level and the factors affecting physical activity among young adults who are socially isolated due to coronavirus.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 1206
• Est. completion date: May 31, 2020
• Est. primary completion date: May 31, 2020
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 50 Years

Eligibility

Inclusion Criteria:

• Being between the ages of 18-50

• Being volunteer

Exclusion Criteria:

• Being unable to communicate in Turkish

• Not knowing read and write in Turkish

Related Conditions & MeSH terms

• Social Isolation

Locations

Country	Name	City	State
Turkey	Özge Ertan	Istanbul

Sponsors (1)

Lead Sponsor	Collaborator
Istanbul University-Cerrahpasa

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Exercise Habit and Factors Affecting Exercise Attendance	It was created by the researchers due to the fact that the existing surveys could not meet the pandemic period. It will be questioned whether the participants had exercise habits in the times before the pandemic. Possible reasons will be questioned according to the positive and negative answers. The answers of the questions are yes / no and they will not be scored. Frequency evaluation will be made according to the results obtained.	The assessment will be made once at baseline, data collection will be completed up to 6 weeks.
Secondary	International Physical Activity Questionnaire - Short Form (IPAQ-SF)	IPAQ-SF provides information on walking, moderate and vigorous activities and time spent sitting, within a week. There are two forms of output from scoring the IPAQ. Results can be reported in categories (low activity levels, moderate activity levels or high activity levels) or as a continuous variable (MET minutes a week). MET minutes represent the amount of energy expended carrying out physical activity.	The assessment will be made once at baseline, data collection will be completed up to 6 weeks.
Secondary	Exercise Benefits/Barriers Scale	It was developed in response to a need for an instrument to determine perceptions of individuals concerning the benefits and barriers to participating in exercise. The scale, which is a 4-point Likert type, has 4 responses from 4 (strongly agree) to 1 (strongly disagree). The total score of the scale varies between 43-172. Higher scores mean that knowing the benefits of exercise and no barrier to exercise.	The assessment will be made once at baseline, data collection will be completed up to 6 weeks.
Secondary	The Pittsburgh Sleep Quality Index	The Pittsburgh Sleep Quality Index (PSQI) is a self-report questionnaire that assesses sleep quality over a 1-month time interval. It consists of 24 questions, 18 of which are included in the scoring. Each question is scored between 0-3 and the highest total score is 21. The high total score indicates poor sleep quality.	The assessment will be made once at baseline, data collection will be completed up to 6 weeks.
Secondary	The Hospital Anxiety and Depression Scale	A self-assessment scale has been developed and found to be a reliable instrument for detecting states of depression and anxiety. The questions of the scale, which is a 4-point Likert type, are scored between 0-3. The total score is obtained between 0-21. The high score indicates the presence of depression and anxiety.	The assessment will be made once at baseline, data collection will be completed up to 6 weeks.