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

Sponsor
Dr. Soetomo General Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT05246124
Collaborator
Universitas Airlangga (Other)
61
1
2
19
97.7

Study Details

Study Description

Brief Summary

This was a randomized controlled trial study to measure the effect of intervention of Zumba dance towards psychological and biological markers in hospital residents managing COVID-19 patients

Condition or Disease Intervention/Treatment Phase
  • Other: Zumba dance exercise
N/A

Detailed Description

A study to compare the effect of Zumba dance exercise towards psychological and biological markers in control and intervention groups of residents managing COVID-19 patients. Psychological markers were assessed using State Trait Anxiety Inventory (STAI), Brief Resilience Scale (BRS), and Maslach Burnout Inventory (MBI) questionnaires. Biological markers being measured were neutrophil to lymphocyte ratio (NLR), CD4, Interleukin-6 (IL-6), and salivary cortisol. Measurements were done at the beginning of self-isolation after shift and 2 weeks after self-isolation.

Study Design

Study Type:
Interventional
Actual Enrollment :
61 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
The Effect of Demographic, Mental, and Physical Activity Profiles Towards Burnout in Frontline Healthcare Workers Facing COVID-19 Pandemics in RSUD Dr. Soetomo Surabaya
Actual Study Start Date :
May 25, 2020
Actual Primary Completion Date :
Jun 13, 2020
Actual Study Completion Date :
Jun 13, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: 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

Other: 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

No Intervention: Control group

No intervention during 2-week self-isolation period

Outcome Measures

Primary Outcome Measures

  1. State-Trait Anxiety Inventory (STAI) [2 weeks]

    State anxiety (STAI-S) is the presence subjective feeling of fear and tension, also the occurrence of autonomic nervous activation responding to dangerous or threatening condition. Trait anxiety (STAI-T) is a more stable aspect of tendency towards anxiety, including calmness, self-esteem, and feeling secure. STAI contains 40 statements with the score interpretation ranging from 20-80. The score between 20-37 means having low or no anxiety, 38-44 indicates medium anxiety, and 45-80 suggests high anxiety

  2. Brief Resiliency Scale (BRS) [2 weeks]

    BRS consists of six questions, with three positive statements and three negative statements. Participants choose one of the five responses to the statements, ranging from "strongly disagree" to "strongly agree". There are three categories of results: low

  3. Maslach Burnout Inventory (MBI) [2 weeks]

    The MBI scoring is divided into dimensions of burnout such as emotional exhaustion (EE), depersonalization (DP), and personal accomplishment (PA). The 22-items questionnaire evaluates these domains of burnout, containing 9 items for emotional exhaustion (MBI-EE), 5 items for depersonalization (MBI-DP), and 8 items for personal accomplishment (MBI-PA). Each item is rated using a Likert scale, measuring the experience of the participants, ranging from never (0) to everyday (6). The MBI-EE score consists of high for total score ≥ 30, moderate for 18-28, and low for ≤ 17. The MBI-DP score comprises high for total score ≥ 12, moderate for 6-11, and low for ≤ 5. As for the MBI-PA, it is considered low for a total score ≤ 33, moderate for 34-39, and high for ≥ 40

  4. Cortisol [2 weeks]

    Unstimulated saliva samples, using the passive drooling method, were collected from each participant. The participants should not eat or drink anything at least 1 hour prior to the saliva collection. Also, the participants were instructed to brush their teeth and wash their oral cavities with sterilized water. Samples were kept cold using cooler box and transported to the laboratory. In the laboratory, samples were immediately centrifuged 1700xg at 4°C for 10 minutes within one hour after collection, Samples were aliquoted and stored at -80°C for further analysis of cortisol level. Determination of saliva cortisol was performed using a cortisol enzyme immunoassay kit. Samples (25 µL) were treated according to the manufacturer's instructions. The optical density of the samples and standards were measured at a wavelength of 450 nm by a microplate reader

  5. CD4 [2 weeks]

    5 ml blood samples were collected from median cubital vein using a standardized venipuncture technique in EDTA tube for CD4 analysis. Blood samples were centrifuged 2500 rpm for 15 minutes. The serum were then aliquoted and stored at -80°C. CD4 were analyzed by flowcytometry according to the manufacturer's instruction.

  6. Interleukin-6 (IL-6) [2 weeks]

    5 ml blood samples were collected from median cubital vein using a standardized venipuncture technique in serum separator tube (SST) for Interleukin 6. Blood samples were centrifuged 2500 rpm for 15 minutes. The serum were then aliquoted and stored at -80°C. Quantification of Interleukin-6 used commercial ELISA kit according to the manufacturer's instructions. The optical density of the samples and standards were measured by a microplate reader. Samples' concentration was calculated according to the relevant standard curve.

  7. Neutrophil to lymphocyte ratio (NLR) [2 weeks]

    5 ml blood samples were collected from median cubital vein using a standardized venipuncture technique in EDTA tube for NLR analysis. NLR were analyzed by flowcytometry according to the manufacturer's instruction.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Residents of anesthesiology and internal medicine department at Dr. Soetomo General Hospital Surabaya

  • Residents managing COVID-19 patients in the special isolation room

Exclusion Criteria:
  • Residents that did not fill in the questionnaires completely

  • 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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Dr. Soetomo General Hospital Surabaya East Java Indonesia 67161

Sponsors and Collaborators

  • Dr. Soetomo General Hospital
  • Universitas Airlangga

Investigators

  • Principal Investigator: Margarita M Maramis, MD, Ph.D, Dr. Soetomo General Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Dr. Soetomo General Hospital
ClinicalTrials.gov Identifier:
NCT05246124
Other Study ID Numbers:
  • 0006/KEPK/V/2020
First Posted:
Feb 18, 2022
Last Update Posted:
Feb 22, 2022
Last Verified:
Feb 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Dr. Soetomo General Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 22, 2022