- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05779501
Efficacy of Internet-delivered Strengths Use Intervention
Testing the Efficacy of an Internet-delivered Strengths Use Intervention in Organizations A Waiting-list Randomized Trial
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Timis
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Timisoara, Timis, Romania, 300223
- West University of Timisoara
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Not other than the age of the participants.
Exclusion Criteria:
- Lack of internet access during the period of the implementation of the program (prescreened during enrolment).
Controlled variables:
- Participants levels of work engagement and work experience will be controlled for by stratified randomization. For each of the two factors we will created three strata (low level: lowest - 33rd percentile; moderate level: 34th - 66th percentile; high level: 67th percentile - highest), and the randomization will be applied for each stratum.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Sequential Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Intervention group
The experimental arm will receive the online strengths use intervention program over a period of 4 weeks, through an LMS software solution.
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The online strengths use intervention program follows the theorized five stages of strengths use interventions: (1) preparation and commitment, (2) identification, (3) integration, (4) action, and (5) evaluation. To increase participant engagement and motivation, gamification components are embedded in several stages. The intervention was previously tested through a feasibility and acceptability trial (NCT05474807). The entire intervention will be delivered online via an LMS software solution. |
Other: Waiting-list control group
The waiting-list control arm will receive the same intervention immediately after the intervention group finishes and will have filled in the post-test outcomes measures.
|
The waiting-list arm will serve as the control group, filling in only the outcome measure at the same time as the intervention group participants. After the intervention group finishes participating in the intervention, the waiting-list participants will benefit from the same internet-delivered strengths use program. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Work engagement
Time Frame: Change from baseline to mid-intervention and post-intervention (approximately 3 weeks and 6 weeks).
|
Work engagement will be measured with the Utrecht Work Engagement Scale (UWES-9).
It has 9 items that form three dimensions, each with 3 items: vigor (e.g., "At my work, I feel bursting with energy"), dedication (e.g., "I am enthusiastic about my job"), and absorption (e.g., "I am immersed in my work").
This measure uses a 7-point scale (0 =never, 6 = always).
Higher scores represent higher work engagement.
|
Change from baseline to mid-intervention and post-intervention (approximately 3 weeks and 6 weeks).
|
Psychological capital (PsyCap)
Time Frame: Change from baseline to mid-intervention and post-intervention (approximately 3 weeks and 6 weeks).
|
Psychological capital will be measured with the 12-item Psychological Capital Questionnaire.
It has four subscales: hope ("At the moment, I feel quite fulfilled at work."), self-efficacy ("I feel confident presenting information to a group of colleagues."),
resilience ("Usually, at work, I easily get over the stressful aspects."),
and optimism ("I am optimistic about what will happen to me in the future regarding my job.").
All 12-item are reported on a 6-point Likert scale (1 = strongly disagree, 6 = strongly agree).
Higher scores represent higher PsyCap.
|
Change from baseline to mid-intervention and post-intervention (approximately 3 weeks and 6 weeks).
|
Strengths use
Time Frame: Change from baseline to mid-intervention and post-intervention (approximately 3 weeks and 6 weeks).
|
The Strengths Use subscale from the Strengths Use and Deficit Correction questionnaire (SUDCO).
I has 6 items, rated on a 0 (almost never) to 6 (almost always) scale.
A sample item is "I seek opportunities to do my work in a manner that best suits my strong points".
Higher scores represent higher levels of strengths use.
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Change from baseline to mid-intervention and post-intervention (approximately 3 weeks and 6 weeks).
|
Strengths identification, use and development
Time Frame: Change from baseline to mid-intervention and post-intervention (approximately 3 weeks and 6 weeks).
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A set of 18 items, rated on a 0 (almost never) to 6 (almost always) scale, was developed by the team of experts involved in this study.
Higher scores represent higher levels of strengths use, identification, and development.
|
Change from baseline to mid-intervention and post-intervention (approximately 3 weeks and 6 weeks).
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Burnout
Time Frame: Change from baseline to post-intervention (approximately 6 weeks).
|
Burnout will be assessed with the 12-item Burnout Assessment Tool (BAT).
This questionnaire has four subscales: exhaustion (3 items; "At work, I feel mentally exhausted."),
emotional impairment (3 items; "At work, I feel unable to control my emotions."),
cognitive impairment (3 items; "At work, I have trouble staying focused.")
and mental distance (3 items; "I struggle to find any enthusiasm for my work.").
All items are scored on a 5-point scale ranging from 1(never) to 5 (always).
Higher scores represent elevated symptoms of burnout.
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Change from baseline to post-intervention (approximately 6 weeks).
|
Job satisfaction
Time Frame: Change from baseline to post-intervention (approximately 6 weeks).
|
Job satisfaction will be measured with the Michigan Organizational Assessment Questionnaire.
The scale has three items with a response on a 7-point Likert scale (1 = total disagreement, 7 = total agreement).
A sample item reads: "In general, I like working here.".
Higher scores represent higher job satisfaction.
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Change from baseline to post-intervention (approximately 6 weeks).
|
Job performance
Time Frame: Change from baseline to post-intervention (approximately 6 weeks).
|
Job performance will be assessed with a 7-item scale.
Response options range on a Likert scale from 1 (strongly disagree) to 5 (strongly agree).
A sample item is "I adequately complete my assigned duties.".
Higher scores represent higher performance.
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Change from baseline to post-intervention (approximately 6 weeks).
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Employability
Time Frame: Change from baseline to post-intervention (approximately 6 weeks).
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Employability will be measured with the four-item Perceived Employability Scale.
Each item is rated on a 5-point Likert scale (1 = totally disagree; 5 = totally agree).
Higher scores represent higher levels of employability.
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Change from baseline to post-intervention (approximately 6 weeks).
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Life satisfaction
Time Frame: Change from baseline to post-intervention (approximately 6 weeks).
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Life satisfaction will be measured with the five items of the Satisfaction with Life Scale.
All answers are reported on a 7-point Likert scale (1 = totally disagree; 7 = totally agree); one item example being, "I am satisfied with my life".
Higher scores represent higher satisfaction with life.
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Change from baseline to post-intervention (approximately 6 weeks).
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Satisfaction with the intervention
Time Frame: At study completion (post-intervention), an average of 6 weeks.
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Satisfaction with the intervention will be measured using 38 items.
A higher score means a better outcome (increased satisfaction with the intervention).
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At study completion (post-intervention), an average of 6 weeks.
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Satisfaction with the intervention
Time Frame: At study completion (post-intervention), an average of 6 weeks.
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7 open-ended questions exploring participants' subjective experience with the intervention program.
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At study completion (post-intervention), an average of 6 weeks.
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Collaborators and Investigators
Sponsor
Publications and helpful links
General Publications
- Schaufeli WB, Desart S, De Witte H. Burnout Assessment Tool (BAT)-Development, Validity, and Reliability. Int J Environ Res Public Health. 2020 Dec 18;17(24):9495. doi: 10.3390/ijerph17249495.
- Tulbure BT, Rusu A, Sava FA, Salagean N, Farchione TJ. A Web-Based Transdiagnostic Intervention for Affective and Mood Disorders: Randomized Controlled Trial. JMIR Ment Health. 2018 May 24;5(2):e36. doi: 10.2196/mental.8901.
- Van Woerkom, M., Mostert, K., Els, C., Bakker, A. B., De Beer, L., & Rothmann Jr, S. (2016). Strengths use and deficit correction in organizations: Development and validation of a questionnaire. European Journal of Work and Organizational Psychology, 25(6), 960-975. https://doi.org/10.1080/1359432X.2016.1193010
- Watson D, Clark LA. Negative affectivity: the disposition to experience aversive emotional states. Psychol Bull. 1984 Nov;96(3):465-90. No abstract available.
- Williams, L. J., & Anderson, S. E. (1991). Job satisfaction and organizational commitment as predictors of organizational citizenship and in-role behaviors. Journal of management, 17(3), 601-617. https://doi.org/10.1177/014920639101700305
- Camman, C., Fichman, M., Jenkins, D., & Klesh, J. (1979). The Michigan Organizational Assessment Questionnaire(University of Michigan, Ann Arbor, Michigan).
- Luthans, F. L., Avolio, B. J., & Avey, J. A. (2007). Psychological Capital Questionnaire (PsyCap) [Database record]. APAPsycTests. https://doi.org/10.1037/t06483-000
- Schaufeli, W. B., Bakker, A. B., & Salanova, M. (2006). The measurement of work engagement with a short questionnaire: Across-national study. Educational and psychological measurement, 66(4), 701-716.https://doi.org/10.1177/0013164405282471
- Miglianico, M., Dubreuil, P., Miquelon, P., Bakker, A. B., & Martin-Krumm, C. (2020). Strength use in the workplace: aliterature review. Journal of Happiness Studies, 21(2), 737-764. https://doi.org/10.1007/s10902-019-00095-w
- De Witte, H. (1992). Tussen optimisten en teruggetrokkenen. Een empirisch onderzoek naar het psychosociaal profiel vanlangdurig werklozen en deelnemers aan de Weer-Werkactie in Vlaanderen [Between optimists and withdrawns. An empiricalinvestigation of the psychosocial profile of longterm unemployed and participants of the Back-to-Work Program in Flanders].Leuven, Belgium: HIVA
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
- MEGSIS S3 RCT
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
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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