- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03256682
The Efficacy of Mobile Video Counseling for Employees With Emotional Labor
The Efficacy of a Mobile Video Counseling Targeted for Stress Reduction and Resilience Enhancement in Employees With Emotional Labor
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
After screening, Pre-evaluation is conducted on the subjects who agreed to participate in the study. Pre-assessment includes questionnaires related to stress, emotional labor, resilience, sleep, etc., and includes stress-related physiological measures using HRV, 2 lead EEG. After the pre-evaluation, the test group will conduct a counseling program with a psychologist for 50 minutes at a time, once a week, for a total of 4 sessions (one month for a period). The place should be placed in a quiet place where the subject thinks comfortably and is designated as the same place to exclude the influence by the place, but the subject does not have to visit the hospital. In the offline counseling group, four counseling sessions are held with the psychologist off-line for a total of 4 counseling sessions, 50 minutes at a time, once a week after the same pre-evaluation. As a self-care control, counseling is not provided and self-learning materials are provided once a week.
Mobile counseling group and offline counseling group visit the hospital within one week after termination and within 4 to 5 weeks after pre-evaluation in self-care control group. Also, to see if the effect of mobile counseling is continued even after counseling is completed, visit the counseling clinic one month after counseling is over and conduct the same test. The data obtained from this study showed that the mobile counseling program measured the change in the clinical scale and heart rate variability and EEG such as the stress and resilience of the subjects, and the self-care group using the offline counseling group and stress data and stress related psychological and physiological And compare the effects on the improvement of the indicator.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Gyeonggi-do
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Seongnam, Gyeonggi-do, Korea, Republic of, 13605
- Seoul National University Bundang Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Workers over the age of 19 and under 65
- In the Perceived Stress Scale 14 points or more
- If you are currently taking medication due to psychiatric illnesses such as depression, anxiety disorder, insomnia, etc., if the stabilizer is expected to have no change in drug dose during the clinical trial
- If you understand the protocol and voluntarily agree to participate
- If you have an Android phone
Exclusion Criteria:
- Age under 19, adult over 65
- If you have dementia, intellectual disability, or other cognitive impairment
- If you have convulsive disorder, stroke, or other neurological disorder
- If you have psychosis such as schizophrenia or bipolar disorder or you have a history
- If you have a disease that can affect the reliability of HRV test, such as heart disease or lung disease.
- Has received non-pharmacological psychiatric or counseling treatment within the current or last 6 months.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Mobile Video Counseling
Utilize mobile imaging equipment, receive a total of 4 stress management consultations every 50 minutes at a time, once a week.
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stress management counseling based on CBT and relaxation
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Active Comparator: Offline Counseling
Receive a total of 4 stress management counseling, once a week for 50 minutes each session.
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stress management counseling based on CBT and relaxation
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|
No Intervention: Selfcare
Use stress management materials to manage yourself.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from baseline Perceived Stress Scale (PSS) score at 4, 8 weeks
Time Frame: Baseline and after 4, 8 weeks later
|
14-item scale developed by Cohen et al. (1983) that emphasizes subjective perception of stress.
Measures the degree of perceived unforeseeable, uncontrollable, and overwhelming experience of stress in the past month.
|
Baseline and after 4, 8 weeks later
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from baseline Korean Emotional Labor Assessment Tool score at 4, 8 weeks
Time Frame: Baseline and after 4, 8 weeks later
|
The total of 26 items were Emotional expression and control 5 items, organizational monitoring and management system 4 items, forced customer response 4 items, emotional damage 6 items, organizational protection system 7 items, and organizational protection system is reverse coding and summed up. 4 point Likert scale (1 = not at all, 5 = very much), and the possible total score ranges from 26 to 130 points.
The higher the score, the more emotional labor means.
|
Baseline and after 4, 8 weeks later
|
|
Change from baseline Korean abbreviation of Occupational Stress Scale (KOSS) score at 4, 8 weeks
Time Frame: Baseline and after 4, 8 weeks later
|
total of 24 items were used, and each item was not at all (from 1 point) to very much (5 points).
The higher the score, the more the job stress means.
Job demand, Insufficient job control, job insecurity, interpersonal conflict, Organizational system, Lack of reward and Occupational climate.
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Baseline and after 4, 8 weeks later
|
|
Change from baseline Patient Health Questionnaire 9 (PHQ-9) score at 4, 8 weeks
Time Frame: Baseline and after 4, 8 weeks later
|
The total score is 0 to 27, and the higher the total score, the more severe the depressive symptoms.
Cutpoints of 5, 10, 15 and 20 represent the thresholds for mild, moderate, moderate severe, and severe depression, respectively.
|
Baseline and after 4, 8 weeks later
|
|
Change from baseline Brief resilience scale (BRS) score at 4, 8 weeks
Time Frame: Baseline and after 4, 8 weeks later
|
It is composed of 6 questions and is evaluated on the 5-point scale (1: not at all, 5: very much)
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Baseline and after 4, 8 weeks later
|
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Change from baseline Athens Insomnia Scale (AIS) score at 4, 8 weeks
Time Frame: Baseline and after 4, 8 weeks later
|
total score of 6 points was used as a breakpoint, this Using the quality index of Pittsburgh Sleep, which is widely used to evaluate the quality of sleep
|
Baseline and after 4, 8 weeks later
|
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Change from baseline Depression, Anxiety, Stress Scale (DASS) score at 4, 8 weeks
Time Frame: Baseline and after 4, 8 weeks later
|
A total of 21 questions, depression, anxiety, and stress were assessed on a 4-point scale (0: not at all, 3: very or almost always).
In this study, only 7 items relating to anxiety were extracted.
The lowest score is from 0 to the maximum score of 21, and the higher the score, the more severe anxiety.
Anxiety scores above 8 indicate significant anxiety symptoms
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Baseline and after 4, 8 weeks later
|
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Change from baseline Connor-Davidson Resilience Scale (CD-RISC) score at 4, 8 weeks
Time Frame: Baseline and after 4, 8 weeks later
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A total of 25 items were assessed as a 5-point Likert scale (0: not at all, 4: very much).
A score of 0-100 means higher resilience
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Baseline and after 4, 8 weeks later
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Change from baseline Maslach Burnout Inventory-General Survey (MBI-GS) score at 4, 8 weeks
Time Frame: Baseline and after 4, 8 weeks later
|
Evaluate on a total of 16 questions on a 7 point scale (1 point = not at all, 7 points = very much).
The higher the total score, the greater the degree of job exhaustion.
|
Baseline and after 4, 8 weeks later
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Change from baseline Heart rate variability (HRV) and Change from baseline Eletroencephalogram (EEG) score at 4, 8 weeks
Time Frame: Baseline and after 4, 8 weeks later
|
The instrument measures the EEG from the headset forehead sensor (EEG measurement of the prefrontal lobe, 2 channel EEG) and measures the pulse at the earlobe (measure the pulse rate in the earlobe vessel using a light sensor).
The results of EEG and heart rate variability were calculated by measuring for 5 minutes.
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Baseline and after 4, 8 weeks later
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Counseling Satisfaction Scale
Time Frame: After 4 weeks intervention
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Evaluate within 7 days of closing psychological counseling.
Twelve questions to evaluate the quality of psychological counseling, content, psychological counselor 's attitude, procedures, and six questions to measure accessibility and a written description question for the proposal.
The mobile group further includes questions such as system speed, image quality, sound and so on.
Evaluating from not at all (1 point) very much (5 points), which means that the higher the score is, the higher the degree of satisfaction is.
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After 4 weeks intervention
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Change from baseline Working Memory score at 4, 8 weeks
Time Frame: Baseline and after 4, 8 weeks later
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Measure short-term memory, work function known to be sensitive to stress.
It consists of forward, backward, sequencing, scored 0 - 14 points, and means that the higher the score, the better the function.
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Baseline and after 4, 8 weeks later
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Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Jeong Hyun Kim, MD, Ph.D, Seoul National Univerysity Bundang Hospital
Publications and helpful links
General Publications
- Kunzler AM, Helmreich I, Chmitorz A, Konig J, Binder H, Wessa M, Lieb K. Psychological interventions to foster resilience in healthcare professionals. Cochrane Database Syst Rev. 2020 Jul 5;7(7):CD012527. doi: 10.1002/14651858.CD012527.pub2.
- Kim JI, Yun JY, Park H, Park SY, Ahn Y, Lee H, Kim TK, Yoon S, Lee YJ, Oh S, Denninger JW, Kim BN, Kim JH. A Mobile Videoconference-Based Intervention on Stress Reduction and Resilience Enhancement in Employees: Randomized Controlled Trial. J Med Internet Res. 2018 Oct 22;20(10):e10760. doi: 10.2196/10760.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- B-1707-408-305
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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