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Not yet recruitingNCT06944990Updated Apr 25, 2025

Meta Self-efficacy Internet Intervention to Improve Work Self-efficacy and Occupational Well-being in Young Employees

An interventional study of Meta self-efficacy internet intervention and Placebo in Self Efficacy, Occupational Stress and Well-Being, Psychological, sponsored by University of Social Sciences and Humanities, Warsaw. Not yet recruiting at 1 site in Poland. Open to participants aged 18 Years to 30 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-04-25.

Sponsored by University of Social Sciences and Humanities, Warsaw · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
600
Allocation
Randomized
Ages
18 Years to 30 Years
Sex
All
01

Study summary

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.

Read the 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.

02

Conditions studied

  • Self Efficacy
  • Occupational Stress
  • Well-Being, Psychological
  • Work Related Stress

Keywords

  • meta self-efficacy
  • self-efficacy
  • job affective well-being
  • sustainable employability
  • work stress
  • work self-efficacy
03

In context

Occupational Stress

236 studies on the registry are indexed under Occupational Stress; 63 are open to participants now.

This study's planned enrollment of 600 is above the median of 84 across 168 interventional studies indexed under Occupational Stress.

Browse Occupational Stress studies →

Lead sponsor

University of Social Sciences and Humanities, Warsaw is the lead sponsor of 25 studies on the registry; 10 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 30 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

Exclusion Criteria:

  • none
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
600 participants (estimated)

Study arms

  • 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.

    Behavioral: Meta self-efficacy internet intervention

  • Placebo comparator
    Placebo

    The placebo condition contains educational material delivered with the same modality as in the experimental condition.

    Behavioral: Placebo

Interventions

  • BehavioralMeta 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.

  • BehavioralPlacebo

    The placebo condition contains educational material delivered with the same modality as in the experimental condition.

06

What researchers measure

Primary outcomes

  1. Work Self-Efficacy

    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).

    Time frame: Posttest (after 3 weeks), 3-months follow-up, 6-months follow-up

Secondary outcomes

  1. Job Affective Well-Being

    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).

    Time frame: Posttest (after 3 weeks), 3-months follow-up, 6-months follow-up

  2. Job Stress

    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.

    Time frame: Posttest (after 3 weeks), 3-months follow-up, 6-months follow-up

  3. Work Capabilities

    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).

    Time frame: Posttest (after 3 weeks), 3-months follow-up, 6-months follow-up

Other outcomes

  1. Meta self-efficacy.

    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.

    Time frame: Posttest (after 3 weeks), 3-months follow-up, 6-months follow-up

07

Study locations

1 site
  • SWPS University of Social Sciences and Humanities
    Warsaw, 00-864, Poland
08

References and documents

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. PubMed 847061 ↗
  • 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. PubMed 33427674 ↗

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 25, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06944990
Lead sponsor
University of Social Sciences and Humanities, Warsaw
Responsible party
Jan Maciejewski (Principal Investigator, University of Social Sciences and Humanities, Warsaw) — Principal investigator
First posted
Apr 25, 2025
Start date
Mar 1, 2026 (estimated)
Primary completion
Dec 1, 2027 (estimated)
Completion
Dec 1, 2027 (estimated)
Last update
Apr 25, 2025

Study contacts

Jan Maciejewski
Contact
jmaciejewski1@swps.edu.pl
+48690688375
Jan Maciejewski
principal investigator · SWPS University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Apr 2025. You cannot join it, but the record below documents what was studied.

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