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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05942898
Other study ID # 2023-02
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 25, 2023
Est. completion date December 31, 2023

Study information

Verified date February 2024
Source International Institute of Behavioral Medicines
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This is a behavioral observational study aimed at evaluating the impact that anxiety exerts on working people at the moment of awakening in the morning. It consists of a short self-administered questionnaire which will be given to workers to complete. Relationships between workers' answers and anxiety will be evaluated.


Description:

This is a behavioral observational study aimed at evaluating the impact that anxiety exerts on working people at the moment of awakening in the morning. Literature found out that anticipatory anxiety plays a key role as for awakening quality (experiencing self). This evaluation could change at the end of the working day due to biased memory effects (remembering self). In Literature there are not studies which investigate the relationships between time to awakening before the alarm sounds and anxiety. The study consists of a short self-administered questionnaire which will be given to workers to complete. In more details, the survey is made of five questions collecting information on type of work, people who use an alarm, time of awakening before the alarm goes off, feelings on the moment of awakening, and feelings as for the working day spent. Further, participants will have to complete an anxiety self-administered questionnaire on anxiety, and namely the Zung Self-Rating Anxiety Scale. Descriptive statistics will be presented by taking into account the characteristics of the sample being investigated. Statistical correlations between workers' answers and anxiety will be also evaluated. This study's usefulness relies on detecting on advance mood disorders (like anxiety is) and maladaptive behaviors, in order to build persons' positive routines (i.e. well-being) and improve their productive quality at work.


Recruitment information / eligibility

Status Completed
Enrollment 135
Est. completion date December 31, 2023
Est. primary completion date November 30, 2023
Accepts healthy volunteers
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - Being workers (any type) - Adult age - Ability to understand the Italian language Exclusion Criteria: - People who do not use the alarm clock to wake up in the morning - Refuse to adhere to the study

Study Design


Related Conditions & MeSH terms


Intervention

Other:
The present study does not contain any intervention
The present study does not contain any intervention

Locations

Country Name City State
Italy Barbara Rocca Calosso

Sponsors (1)

Lead Sponsor Collaborator
International Institute of Behavioral Medicines

Country where clinical trial is conducted

Italy, 

References & Publications (1)

Dunstan DA, Scott N. Norms for Zung's Self-rating Anxiety Scale. BMC Psychiatry. 2020 Feb 28;20(1):90. doi: 10.1186/s12888-019-2427-6. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Zung Zung Self-Rating Anxiety Scale; score 20-80 with higher estimates indicating higher levels of anxiety At the specific time of the scale assessment
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