Internet-delivered Strengths Use Intervention

February 26, 2023 updated by: West University of Timisoara

Improving Employee Well-being Through an Internet-delivered Strengths Use Intervention: A Feasibility Study

The aim of the study will be to test the feasibility and acceptability of a novel online-delivered gamification-based intervention for the identification, development, and use of strengths in the organization. The program will be addressed to employees at the beginning of their careers and will have the aim of boosting their well-being and performance.

Study Overview

Study Type

Interventional

Enrollment (Actual)

50

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

Study Locations

    • Timis
      • Timisoara, Timis, Romania, 300223
        • West University of Timisoara

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

18 years to 35 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

- participants should score 4.49 or lower (on a scale from 0 to 6) on work engagement;

Exclusion Criteria:

  • workload which will impede following the intervention program (based on a filter Yes/No question);
  • lack of internet access during the period of the implementation of the program (based on a filter Yes/No question).

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: Other
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

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 6 weeks, through an LMS software solution.

The online strengths use intervention program, will be based on Miglianico et al.'s (2020) general framework, following the theorized five stages: (1) preparation and commitment, (2) identification, (3) integration, (4) action, and (5) evaluation.

As to increase participant engagement and motivation, gamification components will be embedded in several of these stages.

The entire intervention will be delivered online via an LMS software solution.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Work engagement
Time Frame: Change from baseline to post-intervention (approximately 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 agreement scale (0 = never, 6 = always).
Change from baseline to post-intervention (approximately 6 weeks).
Psychological capital (PsyCap)
Time Frame: Change from baseline to post-intervention (approximately 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).
Change from baseline to post-intervention (approximately 6 weeks).
Strengths use
Time Frame: Change from baseline to post-intervention (approximately 6 weeks).
Strengths use will be measured with a set of six items, rated on a 0 (almost never) to 6 (almost always) Likert scale. A sample item is "I seek opportunities to do my work in a manner that best suits my strong points".
Change from baseline to post-intervention (approximately 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 will be scored on a 5-point scale ranging from 1 (never) to 5 (always).
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 scale (1 = total disagreement, 7 = total agreement). A sample item reads: "In general, I like working here.".
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.".
Change from baseline to post-intervention (approximately 6 weeks).
Positive affect
Time Frame: Change from baseline to post-intervention (approximately 6 weeks).
Positive Affect (PA) will be measured with the 10 items of the Positive Affect Negative Affect Schedule (PANAS), representing different types of positive emotions (e.g., "excited", "inspired", and "enthusiastic"). Respondents will be asked to indicate to what extent they experienced these in the time frame of the intervention on a 5-point scale (1 = very slightly or not at all; 5 = very much).
Change from baseline to post-intervention (approximately 6 weeks).
Life satisfaction
Time Frame: Change from baseline to post-intervention (approximately 6 weeks).
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".
Change from baseline to post-intervention (approximately 6 weeks).
Employability
Time Frame: Change from baseline to post-intervention (approximately 6 weeks).
Employability will be measured with the four-item Perceived Employability Scale. Each item is rated on a 5-point liker scale (1 = totally disagree; 5 = totally agree). Higher scores represent higher levels of employability.
Change from baseline to post-intervention (approximately 6 weeks).

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Satisfaction with the intervention
Time Frame: At study completion (post-intervention), an average of 6 weeks.
Satisfaction with the intervention will be measured using 22 items. We will use 6 items aiming at the program's content retrieved from a questionnaire used for measuring the alliance between trainers and trainees. The minimum score is 6 and the highest is 42. A higher score means a better outcome (increased satisfaction with the intervention). Also, we will use 16 items retrieved from a scale previously used for measuring the satisfaction with an online intervention. Nine of the items are measured on a Likert scale. The minimum score is 7 and the maximum is 42. A higher score means greater satisfaction. 7 items are open-ended questions.
At study completion (post-intervention), an average of 6 weeks.
System usability
Time Frame: At study completion (post-intervention), an average of 6 weeks.
We will use a 10-item questionnaire designed to measure participants' satisfaction with the online platform used for the program delivery. The total score of the System Usability Scale ranges between 0 and 100. A higher score means a better outcome.
At study completion (post-intervention), an average of 6 weeks.
Treatment adherence
Time Frame: At study completion (post-intervention), an average of 6 weeks.
The number of completed assignments; Quality of completed assignment (qualitative rating of the degree of completeness and depth of the answer for each assignment, conducted by two independent experts based on apriori established coding grids).
At study completion (post-intervention), an average of 6 weeks.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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

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 (Actual)

November 1, 2022

Primary Completion (Actual)

December 27, 2022

Study Completion (Actual)

December 27, 2022

Study Registration Dates

First Submitted

June 24, 2022

First Submitted That Met QC Criteria

July 22, 2022

First Posted (Actual)

July 26, 2022

Study Record Updates

Last Update Posted (Estimate)

February 28, 2023

Last Update Submitted That Met QC Criteria

February 26, 2023

Last Verified

February 1, 2023

More Information

Terms related to this study

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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