Parental Stress After the Covid-19 Pandemic
1 other identifier
observational
1,440
0 countries
N/A
Brief Summary
The aim of this study is to investigate the levels of parental stress 3 months after (T2) the strict physical distancing government initiated physical distancing protocols related to the COVID-19 pandemic (T1). The study also aims to investigate how predictors measured during the COVID-19 pandemic are associated with parental stress 3 months after when the majority of the protocols are lifted.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jun 2020
Shorter than P25 for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 19, 2020
CompletedFirst Posted
Study publicly available on registry
June 22, 2020
CompletedStudy Start
First participant enrolled
June 22, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 13, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
July 13, 2020
CompletedJune 24, 2020
June 1, 2020
21 days
June 19, 2020
June 22, 2020
Conditions
Outcome Measures
Primary Outcomes (1)
Parental stress
The Danish Parental Stress Scale is developed as a short measure of parental stress consisting of nine items. Three items from this scale were chosen by a panel of clinical experts, with the aim of avoiding topological overlap: 1) I feel overwhelmed by the responsibility of being a parent, 2) The major source of stress in my life is my child(ren), and 3) It is difficult to balance different responsibilities because of my child(ren).
Data is set to be collected starting from 22th of June. The data collection period will last no longer than three weeks depending on the response to the questionnaire
Eligibility Criteria
The participants are parents in the general population.
You may qualify if:
- Eligible participants are all adults with at least one child, including those of 18 years and above
- Who are currently living in Norway and thus experiencing identical NPIs, and
- Who had provided digital consent to partake in the study.
You may not qualify if:
- Children and adolescents (individuals below 18) Adults not residing in Norway during the measurement period
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Oslolead
- Modum Badcollaborator
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Miriam S Johnson, PhD
Oslo Metropolitan University
- PRINCIPAL INVESTIGATOR
Nora Paulsen Skjerdingstad
University of Bergen
- PRINCIPAL INVESTIGATOR
Omid Ebrahimi
University of Oslo & Modum Bad
- PRINCIPAL INVESTIGATOR
Asle Hoffart, PhD
University of Oslo & Modum Bad
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Professer Sverre Urnes Johnson
Study Record Dates
First Submitted
June 19, 2020
First Posted
June 22, 2020
Study Start
June 22, 2020
Primary Completion
July 13, 2020
Study Completion
July 13, 2020
Last Updated
June 24, 2020
Record last verified: 2020-06
Data Sharing
- IPD Sharing
- Will not share