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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06376825
Other study ID # CSV202401
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date April 15, 2024
Est. completion date June 15, 2024

Study information

Verified date April 2024
Source CanSagligi Foundation
Contact Havvanur Uysal Akdemir, MS
Phone +90 (212) 269 66 11
Email havvanur.uysal@cansagligivakfi.org
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this clinical trial is to determine whether an internet-based self-help program reduces burnout in teachers. The study will also evaluate the program's acceptability which means assessing the extent to which users complete the program and find it useful. The main questions it aims to answer are: - Does the program reduce the level of burnout in teachers? - Does the program contribute to an increased sense of meaning for teachers? - How much of the program do teachers finish?


Description:

This concurrent multiple-baseline single-case experimental study aims to assess the efficacy and acceptability of an internet-based self-help program designed to mitigate burnout among teachers. The self-help program, named MyLife, adopts an Acceptance and Commitment Therapy framework and comprises eight modules. Preceding the commencement of the study, the program was tailored to address the specific needs of teachers through collaboration with people with lived experiences and the administration of nationwide surveys. Additionally, the daily questions utilized in this single-case study design were meticulously crafted for this study. In this study no guidance other than reminders will be offered. Participants will be instructed to: - Engage with program content, including audio and text components, every three days over a four-week period. - Respond to daily questions once in day for eight weeks and both before and after the study, utilizing scales and questionnaires. The research questions are as follows: 1. To what extent does the program alleviate burnout among teachers? 2. Does the program foster a heightened sense of meaning in teachers' professional lives? 3. What is the completion rate of the program among participating teachers? 4. Does the program effectively diminish experiential avoidance? Hypotheses: 1. Teachers participating in the MyLife program will experience a significant decrease in burnout levels compared to baseline measures. 2. The MyLife program will lead to a significant increase in the perception of meaning in teachers' professional lives. 3. MyLife program will have a good acceptability. 4. Participation in the MyLife program will be associated with a significant reduction in experiential avoidance among teachers.


Recruitment information / eligibility

Status Recruiting
Enrollment 25
Est. completion date June 15, 2024
Est. primary completion date June 15, 2024
Accepts healthy volunteers No
Gender All
Age group 22 Years to 65 Years
Eligibility Inclusion Criteria: - Being a teacher in Türkiye - Having burnout symptoms related to the workplace. - Able to use e-mail, internet and mobile phone - Able to read fluently in Turkish Exclusion Criteria: - Currently prescribed psychotropic medication or any change in psychotropic medication in last two months - Currently undergoing psychotherapy. - Having thoughts of suicide or self-mutilation.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
MyLife: An internet-based self-help program to reduce burnout
MyLife is a internet-based and Acceptance and Commitment Therapy oriented self-help program to reduce burnout. In this study a tailored to teachers version of the program will be used.

Locations

Country Name City State
Turkey CanSagligi Foundation Center for Contextual Behavioral Science Istanbul

Sponsors (1)

Lead Sponsor Collaborator
Ahmet Nalbant

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Other Daily measures Daily measures will include questions about burnout, valued living and experiential avoidance. Daily questions will be asked during 8 weeks and data will be collected daily.
Primary Burnout Assessment Tool Burnout Assessment Tool is a validated measure which evaluates to what extend people experience burnout in work place. The scale is a 5-point Likert type, meaning "1 = Never" to "5 = Always" (minimum:34 to maxiumum:150). Higher scores from the scale represent higher burnout. Turkish validity and reliability study was conducted and Cronbach's alpha value was stated as 0.95. At baseline and after 8 weeks
Primary Valued Living Questionnaire Valued Living Questionnaire is a validated measure and its aim is to evaluate valued living. The scale consists of 10 items with a 7-point Likert type as 0 = Not at all true and 6 = Completely true (minimum:0; maxiumum:60). The scale, for which Turkish validity and reliability studies have been conducted, has two sub-dimensions: "progress" and "blockage". While the progress subscale expresses that the person takes action in line with his values, the blockage dimension means that the person avoids certain experiences and moves away from a value-oriented life. The Cronbach's alpha value of the Turkish version of the scale was found to be 0.78; as for the progress sub-dimension was 0.77, and for the blockage dimension was 0.76. At baseline and after 8 weeks
Secondary Acceptance and Action Questionnaire-2 AAQ-2 is a measure aiming to evaluate experiential avoidance. The scale consists of 7-point Likert type (minimum:7 to maxiumum 49). Higher points indicate higher experiential avoidance. At baseline and after 8 weeks
Secondary System Usability Scale System Usability Scale aims to measure evaluations of participants about an internet based program. It has 10 items which consists of 5-point Likert-type questions. Higher points indicate better usability of the system (Minimum:0 to maximum:100). After eight weeks
Secondary Attendance rate To evaluate acceptability, participants attendance rate to the program will be recorded. After eight weeks.
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