The Effect of Demographic, Mental, and Physical Activity Profiles Towards Burnout in Frontline Healthcare Workers Facing COVID-19 Pandemics in Dr. Soetomo General Hospital Surabaya
NCT ID: NCT05246124
Last Updated: 2022-02-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
61 participants
INTERVENTIONAL
2020-05-25
2020-06-13
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Healthy Lifestyle or Pro-health Obsession During the Pandemic
NCT04432038
Evaluation of the Efficacy of Aromatherapy on the Well-being of Healthcare Professionals
NCT05373849
Examining the Effects of Art Therapy in Reducing Burnout in Healthcare Providers
NCT04738448
Somatic Mindfulness Training for a Healthy Workforce: Student Pilot Sample
NCT04122534
Impact of Stress Management Training on the Resilience and Stress of Student Nurse Anaesthetists
NCT05867238
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
PREVENTION
TRIPLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Intervention group
This study used Zumba dance exercise done 3 times a week during 2-week self-isolation period, with each session lasting for 50 minutes. The participants did exercise by following instructions from Zumba video shown
Zumba dance exercise
The intervention was Zumba dance done 3 times a week during the 2-week self-isolation period, with each session lasting for 50 minutes. The participants did exercise by following instructions from Zumba video shown
Control group
No intervention during 2-week self-isolation period
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Zumba dance exercise
The intervention was Zumba dance done 3 times a week during the 2-week self-isolation period, with each session lasting for 50 minutes. The participants did exercise by following instructions from Zumba video shown
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Residents managing COVID-19 patients in the special isolation room
Exclusion Criteria
* Residents with comorbidities (diabetes, hypertension, heart disease or autoimmune disorders)
* Residents that were infected with COVID-19
* Residents currently or previously diagnosed with psychosis
* Residents refusing to participate in the study.
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Universitas Airlangga
OTHER
Dr. Soetomo General Hospital
OTHER_GOV
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Margarita M Maramis, MD, Ph.D
Role: PRINCIPAL_INVESTIGATOR
Dr. Soetomo General Hospital
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Dr. Soetomo General Hospital
Surabaya, East Java, Indonesia
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
0006/KEPK/V/2020
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.