Effectiveness of Online Therapy to Prevent Burnout

Sponsor
SciensCollege (Industry)
Overall Status
Completed
CT.gov ID
NCT05343208
Collaborator
Karlstad University (Other), My-E-Health (Other)
50
1
2
1266.9
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Study Details

Study Description

Brief Summary

This study aims to address the reliability and validity of the Empowerment for Participation (EFP) batch of assessments to measure Burnout risk in relation to the efficacy of online interventions to provide proactive rehabilitation using Cognitive Behavioral Therapy (CBT) and floating to achieve improved mental health and wellbeing.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: EFP Psychometric assessment to determine level of afflication
N/A

Detailed Description

An Empirical design using raw EFP psychometric data to measure the effectiveness of online therapy to reduce the risk for Burnout between a control group and an online therapy group. The aim is to test whether or not there is a statistically significant difference in the effectiveness on online therapy to reduce the Risk for Burnout compared to that of a Control Group. Fifty participants were randomly selected. The rehabilitation and control Group consisted of twenty-five normally distributed employees (N25) each. The rehabilitation group received therapy, and the control had not yet received any form of therapy. SPSS was used to analyze the data collected, a Repeated Measure ANOVA, an ANCOVA, a Discriminant analysis, and a Construct Validity analysis were used to test for Reliability and Validity.

The group was randomly selected from a list of employees within the My-E-Health ecosystem. The group (N50) normally distributed group met all assumptions and consisted of a Control Group (N25) and a Therapy Group (N25). The post assessment value was used as the dependent variable.

The Burnout measure (30 questions) is obtained from the Empowerment for Participation (EFP) batch of assessments (110 questions). All assessments and CBT were done digitally online and floating was done at a designated location. The full EFP assessment is integrated into a digital ecosystem designed for this purpose and therapy. The online digital system is an integrity-based platform offering both the employee and caregiver a secure and encrypted ecosystem or secure data tunnel or channel between the therapists and patients.

Study Design

Study Type:
Interventional
Actual Enrollment :
50 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
An empirical and parallel design using raw EFP psychometric data to measure the effectiveness of online therapy to reduce the risk for Burnout between a control group and an online therapy group.An empirical and parallel design using raw EFP psychometric data to measure the effectiveness of online therapy to reduce the risk for Burnout between a control group and an online therapy group.
Masking:
None (Open Label)
Masking Description:
Randomly selected from an employer list
Primary Purpose:
Prevention
Official Title:
Effectiveness of Online Therapy to Prevent Burnout
Actual Study Start Date :
Sep 5, 1916
Actual Primary Completion Date :
Jan 11, 2021
Actual Study Completion Date :
Apr 4, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Cognitive Behavioral Therapy Group

The group received online Cognitive Behavioral Therapy via the My-E-Health. Patients were issued a preTest psychometric assessment and a post therapy assessment using the Burnout Psychometrics provided within the My-E-Health's online ecosystem. All patients were required to validate the accuracy of the assessments during a follow-up of their results.

Diagnostic Test: EFP Psychometric assessment to determine level of afflication
Patients were asked to complete a psychometric assessment in relation to their psychological wellbeing. Results were presented to the patient and validdated by the patient.

No Intervention: Control Group

The Control Group received no online therapy. Patients were issued a preTest psychometric assessment and a post therapy assessment using the Burnout Psychometrics provided within the My-E-Health's online ecosystem. All patients were required to validate the accuracy of the assessments during a follow-up of their results.

Outcome Measures

Primary Outcome Measures

  1. To measure the difference between a pre- and post-assessment score for Burnout in a Control Group versus a Therapy Group. [From admission to discharge, up to 3 months.]

    The Burnout measure (30 questions) is obtained from the Empowerment for Participation (EFP) batch of assessments using Visual Analog Scales (VAS) online. A straight line with a beginning and end point. As the slider moves from left to right, the text positioned at either end of the line increases as the opposite end decreases. The position where the slider stops is represented by a number from 0-20. The risk assessment scale (0-600) determines the level of intervention and preventive care. There are five risk levels of Burnout in relation to the total score following a lineal guide: 0-99 points (M=0-3.300) = No evidence of Burnout, 100-199 points (M=3.333-6.6333) = Low risk for Burnout, 200-299 points (M=6.6667-9.9667) = Moderate risk for Burnout, 300-399 points (M=10.00-13.300) = High risk for Burnout, and 400-600 points (M=13.3333-20) = Burnout. Patient content validation and score accuracy is required after each assessment.

Eligibility Criteria

Criteria

Ages Eligible for Study:
22 Years to 68 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No

Inclusion Criteria

Employees assessed on the EFP Burnout Scale as having:
  • a Moderate Risk of Burnout

  • a High Risk of Burnout

  • A Burned out Risk (Mental Health Exhaustion)

  • Employees with a current Bunrout diagnosis from a hospital, outpatient or psychiatric cllinic

  • A fully employed person with a member organization

  • No other inclusion criteria.

Exclusion Criteria:
Employees assessed on the EFP Burnout Scale as having:
  • No evidence of Burnout

  • Low Risk of Burnout.

  • Unemployed persons

  • No other exclusion critera was used.

Contacts and Locations

Locations

Site City State Country Postal Code
1 SciensCollege Malmö Skåne Sweden 21124

Sponsors and Collaborators

  • SciensCollege
  • Karlstad University
  • My-E-Health

Investigators

  • Principal Investigator: Clive S Michelsen, M.Sc., SciensCollege

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
SciensCollege
ClinicalTrials.gov Identifier:
NCT05343208
Other Study ID Numbers:
  • SC-EOTPB-1
First Posted:
Apr 25, 2022
Last Update Posted:
Apr 25, 2022
Last Verified:
Apr 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by SciensCollege
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 25, 2022