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Evaluation of the Psychosocial Impact on Health Professionals Exposed During COVID 19 Coronavirus Pandemic

Evaluation of the Psychosocial Impact on Health Professionals Exposed During the COVID 19 Coronavirus Pandemic

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04752839
Enrollment
300
Registered
2021-02-12
Start date
2021-02-28
Completion date
2021-05-31
Last updated
2021-02-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety, Coronavirus Infection, COVID, Depression, Post Traumatic Stress Disorder, Psychological Stress, Psychosocial Impairment

Keywords

Covid 19, Healthcare workers, Mental health

Brief summary

Application of a survey in electronic support to hospital professionals. This survey will include different demographics as well as questions from own elaboration about the different aspects related to the development of work during the health emergency. A third part will be included different validated scales for screening / diagnosis of different problems that can present those who are working in the Current situation. The different scales are the PHQ-9, GAD 7, ISI, and EIE-R. These scales address the different problems that have been seen that can introduce professionals, Depression, Anxiety, Insomnia and adaptation to stressors.

Interventions

None listed

Sponsors

Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Workers during COVID 19 pandemic at Hospital de la Creu i Sant Pau

Exclusion criteria

* No

Design outcomes

Primary

MeasureTime frameDescription
General Anxiety Disorder (GAD7) score.Through study completion, an average of 1 year.This instrument has been created to serve as a screening in anxiety disorder widespread. It is composed of 7 Likert-type response items from 0 to 3 that include the symptoms and the disability associated with the disorder.7 For its correction, a total score is obtained from the sum of scores of all the items, which can range from 0 to 21. There are no established cut-off points for the Spanish version. In the original version, the authors propose a cut-off point of greater than or equal to 10. The version validated for the Spanish population will be used.
Insomnia severity Index (ISI)Through study completion, an average of 1 year.The investigators will use the adaptation of Fernández Mendoza et al. It is made up of 7 items that evaluate the nature, severity and impact of insomnia. It is answered with a Likert-type scale that goes from 0 to 4, taking into account the last month. For its correction, a total score is obtained that ranges between 0 and 28. The proposed cut-off points of the original version are: * 0-7: no insomnia * 8-14: insomnia below the threshold * 15-21: clinical insomnia of moderate severity * 22-28: severe clinical insomnia
Patient Health Questionaire (PHQ-9)Through study completion, an average of 1 year.This instrument is intended to aid the diagnosis of depression through the DSM-IV criteria, and to determine the severity of said disorder. It can also be used to observe the changes experienced by patients over time. It is made up of 9 items with Likert-type responses with values between 0 and 3 that refer to the last two weeks. For its correction, a total score is obtained that ranges between 0 and 27. The proposed cut-off points are: * 1-4: minimal depression * 5-9: mild depression * 10-14: moderate depression * 15-19: moderately severe depression * 20-27: severe depression The version validated for the Spanish population will be used
Perceived Stress ScaleThrough study completion, an average of 1 year.The Perceived Stress Scale provides an overall measure of perceived stress in the last month evaluating the degree to which life situations are valued as stressful by people. 12 Specifically: the degree of subjective control over unpredictable or unexpected situations and the discomfort that accompanies the perceived lack of control. Originally it consists of 14 items (some of which are formulated in negative). Two dimensions have been considered (control and loss of control) although more restrictive criteria would require considering the one-dimensionality of the scale. The validated Spanish version will be used.
Impact of Event Scale Revised (IES-R)Through study completion, an average of 1 year.This scale is conceptually based on Horowitz's two-factor theory and assesses the subjective discomfort that accompanies traumatic experiences. It is a self-administered scale, and consists of 22 items in the revised version. 7 items value intrusion 8 avoidance and 7 hyperactivation. The investigators will evaluate the post-traumatic stress symptomatology, and for that, the revised version in Spanish will be used.

Countries

Spain

Contacts

Primary ContactSergio P Pérez, MD
sperezga@santpau.cat678223410
Backup ContactCarla Domínguez, MD
cdominguezg@santpau.cat

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026