- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04772404
Repercussion of the COVID-19 Pandemic on Physical Activity, Psychological State and Sleep
Study Overview
Status
Conditions
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
-
-
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Granada, Spain, 18016
- Recruiting
- Department of Physical Therapy
-
Contact:
- Marie Carmen Valenza, PhD
- Email: cvalenza@ugr.es
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
• Healthy people
Exclusion Criteria:
- Cognitive impairment.
- Diagnose of autism spectrum disorder or severe intellectual disability
- Physical or functional impairment that limits the performance of evaluation
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Knowledge of COVID
Time Frame: Baseline
|
Questionnaire to evaluate the knowledge about COVID-19.
It includes 12 items.
Patients have to answer true/false.
Higher puntuation indicates better knowledge results.
|
Baseline
|
|
Fear of COVID-19 Scale
Time Frame: Baseline
|
Bangla fear of COVID (FCV19-S): It is a questionnaire that assesses the fear of COVID-19.
It consists of 7 items scored on a 5-item Likert scale.
The higher the score, the more fear.
|
Baseline
|
|
COVID-19 Anxiety Scale (CAS)
Time Frame: Baseline
|
Coronavirus anxiety scale (CAS): It is a scale that measures the anxiety generated by COVID-19 in the last two weeks.
It presents 5 items and a score> 9 indicates dysfunctional anxiety associated with the pandemic.
|
Baseline
|
|
COVID Stress Scales
Time Frame: Baseline
|
COVID stress scale (CSS): is a 36-item COVID Stress Scale (CSS) to measure these features, as they pertain to COVID-19.
The CSS were developed to better understand and assess COVID-19-related distress.
The scales were intentionally designed so they could be readily adapted for future pandemics.
|
Baseline
|
|
Burn-Out de Maslach Inventory
Time Frame: Baseline
|
The Maslach Burnout Inventory (MBI) is a psychological assessment instrument comprising 22 symptom items pertaining to occupational burnout
|
Baseline
|
|
Steps per day
Time Frame: Baseline
|
Accelerometer
|
Baseline
|
|
International physical activity questionnaire
Time Frame: Baseline
|
The International Physical Activity Questionnaire (IPAQ) was developed to measure health-related physical activity (PA) in populations.
Higher scores indicates higher physical activity levels.
|
Baseline
|
|
Barriers to being active quiz
Time Frame: Baseline
|
Barriers to being active quiz (BBAQ-21): It is a questionnaire that consists of 21 items.
This questionnaire was aimed at ascertaining perception of barriers against engaging in PA.
|
Baseline
|
|
Questionnaire of the transtheoretical model of change of physical exercise
Time Frame: Baseline
|
Questionnaire of the transtheoretical model of change of physical exercise (QTMCPE): It is made up of 22 items for people who are not physically active and 9 items for physically active people.
It is a Likert-type scale that measures from 1 to 5.
|
Baseline
|
|
Hospital Anxiety and Depression Scale
Time Frame: Baseline
|
Anxiety and depression will be assessed with the Hospital Anxiety and Depression Scale (HADS) .
This scale is composed of 14 items divided into two subscales, 7 items of anxiety and 7 items of depression, involving higher values worse psycho-emotional state.
|
Baseline
|
|
Connor-Davidson Resilience Scale
Time Frame: Baseline
|
Connor-Davidson Resilience Scale (CD-RISC) was used to measure resilience.
It consists of 10 items which form five factors.
Respondents are asked to answer on a five-point Likert scale (0 = totally disagree to 4 = totally agree).
|
Baseline
|
|
COPE-28
Time Frame: Baseline
|
The Brief-COPE is a 28 item self-report questionnaire designed to measure effective and ineffective ways to cope with a stressful life event.
"Coping" is defined broadly as an effort used to minimize distress associated with negative life experiences.
|
Baseline
|
|
Pittsburgh Sleep Quality Index
Time Frame: Baseline
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The Pittsburgh Sleep Quality Index (PSQI) is a self-rated questionnaire which assesses sleep quality and disturbances in the previous month.
|
Baseline
|
|
Morningness-eveningness questionnaire (MEQ)
Time Frame: Baseline
|
Morningness-Eveningness Questionnaire: Consisting of 19 items, the scale was developed to assess individual differences in morningness and eveningness - the degree to which respondents are active and alert at certain times of day.
Scale items query preferences in sleep and waking times, and subjective "peak" times at which respondents feel their best.
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Baseline
|
|
Epworth sleepiness Scale
Time Frame: Baseline
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The ESS asks the respondent to rate on a 4-point scale (0-3) their usual chances of having dozed off or fallen asleep while engaged in eight different activities that differ widely in their somnificity.
|
Baseline
|
|
Insomnia severity index
Time Frame: Baseline
|
Insomnia severity index: It consists of 24 questions that measure sleep disturbances along dimensions: subjective sleep quality, sleep latency (LS), duration, efficiency, sleep disorders, use of sleep medication, and daytime dysfunction.
The evaluation is based on the answers obtained from the previous month.
|
Baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
EuroQoL-5D
Time Frame: Baseline
|
The perception of the level of health and the quality of life were evaluated with the questionnaire European Quality of Life-5 Dimensions (EQ-5D). It is composed of 2 parts in which health status is assessed: Descriptive system: It consists on 5 dimensions that include mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. Patients classify their health status in 3 severity levels: having no problems, having some or moderate problems, being unable to do/having extreme problems. Visual Analog Scale, by which respondents can report their perceived health status with a grade ranging from 0 (the worst possible health status) to 100 (the best possible health status) |
Baseline
|
|
Charlson Comorbidity Index
Time Frame: Baseline
|
Charlson Comorbidity Index predicts the ten-year mortality for a patient who may have a range of comorbid conditions
|
Baseline
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
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
- DF0094UG
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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.
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