Efficacy of Internet-delivered Strengths Use Intervention

October 3, 2023 updated by: West University of Timisoara

Testing the Efficacy of an Internet-delivered Strengths Use Intervention in Organizations A Waiting-list Randomized Trial

The aim of the study will be to test the efficacy of a novel online-delivered gamification-based intervention for the identification, development, and use of strengths in the workplace. The program will be addressed to young employees and will have the aim of boosting their well-being and performance.

Study Overview

Study Type

Interventional

Enrollment (Actual)

167

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 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 39 years (Adult)

Accepts Healthy Volunteers

Yes

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

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: 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.

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.
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).
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.
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.
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.
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 Likert 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
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". Higher scores represent higher satisfaction with life.
Change from baseline to post-intervention (approximately 6 weeks).
Satisfaction with the intervention
Time Frame: At study completion (post-intervention), an average of 6 weeks.
Satisfaction with the intervention will be measured using 38 items. A higher score means a better outcome (increased satisfaction with the intervention).
At study completion (post-intervention), an average of 6 weeks.
Satisfaction with the intervention
Time Frame: At study completion (post-intervention), an average of 6 weeks.
7 open-ended questions exploring participants' subjective experience with the intervention program.
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)

February 15, 2023

Primary Completion (Actual)

August 15, 2023

Study Completion (Actual)

August 15, 2023

Study Registration Dates

First Submitted

February 27, 2023

First Submitted That Met QC Criteria

March 21, 2023

First Posted (Actual)

March 22, 2023

Study Record Updates

Last Update Posted (Actual)

October 5, 2023

Last Update Submitted That Met QC Criteria

October 3, 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)?

UNDECIDED

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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