- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04552392
Psychological Impact of Institutional Quarantine
Psychological Impact of Institutional Quarantine - A Cross-Sectional Observational Study
Study Overview
Detailed Description
Institutional quarantine separates persons who have been potentially exposed to an infectious agent (and thus at risk for disease) from the general community. This may create psychological, emotional, and financial problems for some persons. The experience of those placed under quarantine in terms of compliance, difficulties, emotional response and psychological impact remains under-researched.
In view of the increasing cases of COVID-19 in India and the rising numbers of people being quarantined as a precautionary measure, it was imperative to assess those quarantined for the psychological impact of the concerns regarding this illness and the quarantine procedure. In India, no such study had been undertaken and our study would thus fill the research gap.
The cross-sectional observational study is aimed at assessing the psychological impact of quarantine on Indian Border Security Force (BSF) soldiers (n=100).
The participants will be assessed for depression, anxiety, perceived stress level of impact, and impact of life events using Beck Depression Inventory, State Trait Anxiety Inventory, Perceived Stress Scale, and Impact of Events Scale-Revised respectively. A qualitative interview schedule will be carried out.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Delhi, India
- ITBP Chawala
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Indian-origin adults between the age of 18-60 yrs quarantined at border security force facility
- Both genders would be included
Exclusion Criteria:
- Any chronic co-morbid medical condition
- Current Diagnosis of COVID-19
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
depression
Time Frame: Baseline
|
Beck Depression Inventory
|
Baseline
|
anxiety
Time Frame: Baseline
|
State Trait Anxiety Inventory
|
Baseline
|
perceived stress
Time Frame: Baseline
|
Perceived Stress Scale
|
Baseline
|
impact of life events
Time Frame: Baseline
|
Impact of Events Scale-Revised
|
Baseline
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Pragya Sharma, PhD, Ram Manohar Lohia Hospital
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
Other Study ID Numbers
- COVID
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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