- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06944990
Meta Self-efficacy Internet Intervention to Improve Work Self-efficacy and Occupational Well-being in Young Employees
April 17, 2025 updated by: Jan Maciejewski, University of Social Sciences and Humanities, Warsaw
Meta Self-efficacy Intervention to Improve Work Self-efficacy and Occupational Well-being in Young Employees: Internet Intervention Co-creation and a Randomized Controlled Trial
This randomized controlled trial aims to test whether enhancing meta self-efficacy through a self-guided internet intervention improves young employees' work self-efficacy and occupational well-being.
The trial will evaluate primary (work self-efficacy) and secondary (three dimensions of occupational well-being) outcomes.
It is hypothesized that boosting meta self-efficacy will lead to improvements in outcomes, with effects assessed immediately after the intervention, and at 3- and 6-month follow-ups.
Study Overview
Status
Not yet recruiting
Intervention / Treatment
Detailed Description
This study investigates the efficacy of a self-guided internet intervention designed to enhance meta self-efficacy in young employees.
Meta self-efficacy is a psychological resource that encompasses the ability to leverage self-efficacy sources (mastery experiences, vicarious experiences, persuasion, and affective & physiological states) to boost context-specific self-efficacy.
In this two-arm randomized controlled trial, participants (young employees) will be randomly assigned to an experimental group, which will receive internet intervention with activities aimed at enhancing meta self-efficacy, or to a placebo control group, which will receive educational content.
Primary and secondary outcomes (including work self-efficacy, job stress, job affective well-being, and work capabilities), as well as the manipulation check (meta self-efficacy), will be assessed immediately after the intervention and at 3- and 6-month follow-ups.
The trial aims to evaluate the effect of enhancing meta self-efficacy and explore the impact of factors such as adherence and engagement on the intervention's efficacy.
Study Type
Interventional
Enrollment (Estimated)
600
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Jan Maciejewski
- Phone Number: +48690688375
- Email: jmaciejewski1@swps.edu.pl
Study Locations
-
-
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Warsaw, Poland, 00-864
- SWPS University of Social Sciences and Humanities
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- must be between 18 and 30 years old
- must be empolyed (working at least 20 h / week, for at least the prior two months, regardless of the type of contract)
Exclusion Criteria:
- none
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Meta self-efficacy internet intervention
The meta self-efficacy intervention is a three-week program comprised of activities designed to enhance meta self-efficacy (the ability to leverage self-efficacy sources).
The intervention is contextualized to young employees.
|
The meta self-efficacy intervention is a three-week program comprised of activities designed to enhance meta self-efficacy (the ability to leverage self-efficacy sources).
The intervention is contextualized to young employees.
|
|
Placebo Comparator: Placebo
The placebo condition contains educational material delivered with the same modality as in the experimental condition.
|
The placebo condition contains educational material delivered with the same modality as in the experimental condition.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Work Self-Efficacy
Time Frame: Posttest (after 3 weeks), 3-months follow-up, 6-months follow-up
|
Work Self-Efficacy will be measured with the Work Self-Efficacy scale (WSES).
The questionnaire consists of 26 items.
The responses range from 1 (not at all) to 7 (completely).
|
Posttest (after 3 weeks), 3-months follow-up, 6-months follow-up
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Job Affective Well-Being
Time Frame: Posttest (after 3 weeks), 3-months follow-up, 6-months follow-up
|
Job Affective Well-Being will be measured with the Job Affective Well-Being Scale (JAWS).
The questionaire consists of 12 items.
The responses rage from 1 (never) to 5 (very often).
|
Posttest (after 3 weeks), 3-months follow-up, 6-months follow-up
|
|
Job Stress
Time Frame: Posttest (after 3 weeks), 3-months follow-up, 6-months follow-up
|
Job Stress will be measured with the Perceived Stress Scale (PSS).
The scale consists of 4 items rated on a scale ranging from 0 (never) to 4 (very often).
It will be applied to measure job stress.
The questionnaire's instructions have been modified to align with the occupational context.
|
Posttest (after 3 weeks), 3-months follow-up, 6-months follow-up
|
|
Work Capabilities
Time Frame: Posttest (after 3 weeks), 3-months follow-up, 6-months follow-up
|
Work capabilities will be measured with the Capability Set for Work Questionaire (CSWQ).
The questionaire consists of 7 capabilities, for each there are three aspects to evaluate.
The responses range from 1 (strongly disagree) to 5 (strongly agree).
|
Posttest (after 3 weeks), 3-months follow-up, 6-months follow-up
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Meta self-efficacy.
Time Frame: Posttest (after 3 weeks), 3-months follow-up, 6-months follow-up
|
Meta self-efficacy will be measured with the meta self-efficacy scale (MSES).
The questionnaire consists of 13 items.
The responses range from 0 (cannot do at all) to 10 (certain can do).
Higher score indicates higher level of meta self-efficacy.
|
Posttest (after 3 weeks), 3-months follow-up, 6-months follow-up
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Jan Maciejewski, SWPS University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Bandura A. Self-efficacy: toward a unifying theory of behavioral change. Psychol Rev. 1977 Mar;84(2):191-215. doi: 10.1037//0033-295x.84.2.191. No abstract available.
- Smoktunowicz E, Lesnierowska M, Carlbring P, Andersson G, Cieslak R. Resource-Based Internet Intervention (Med-Stress) to Improve Well-Being Among Medical Professionals: Randomized Controlled Trial. J Med Internet Res. 2021 Jan 11;23(1):e21445. doi: 10.2196/21445.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
March 1, 2026
Primary Completion (Estimated)
December 1, 2027
Study Completion (Estimated)
December 1, 2027
Study Registration Dates
First Submitted
April 11, 2025
First Submitted That Met QC Criteria
April 17, 2025
First Posted (Actual)
April 25, 2025
Study Record Updates
Last Update Posted (Actual)
April 25, 2025
Last Update Submitted That Met QC Criteria
April 17, 2025
Last Verified
April 1, 2025
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- MSE intervention
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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