Internet-delivered Strengths Use Intervention

Sponsor
West University of Timisoara (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05474807
Collaborator
(none)
57
1
2

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Internet-delivered strengths use intervention
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
57 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
One-armed study with baseline and post-intervention measurements.One-armed study with baseline and post-intervention measurements.
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Improving Employee Well-being Through an Internet-delivered Strengths Use Intervention: A Feasibility Study
Anticipated Study Start Date :
Oct 1, 2022
Anticipated Primary Completion Date :
Nov 30, 2022
Anticipated Study Completion Date :
Nov 30, 2022

Arms and Interventions

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.

Behavioral: Internet-delivered strengths use intervention
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.

Outcome Measures

Primary Outcome Measures

  1. Work engagement [Change from baseline to post-intervention (approximately 6 weeks).]

    Work engagement will be measured with the Utrecht Work Engagement Scale (UWES-9; Schaufeli, Bakker, & Salanova, 2006). 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).

  2. Psychological capital (PsyCap) [Change from baseline to post-intervention (approximately 6 weeks).]

    Psychological capital will be measured with the 12-item Psychological Capital Questionnaire (Luthans et al., 2007). 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).

  3. Strengths use [Change from baseline to post-intervention (approximately 6 weeks).]

    Strengths use will be measured with a set of nine items, from the scale proposed by Van Woerkom et al. (2016), 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".

Secondary Outcome Measures

  1. Burnout [Change from baseline to post-intervention (approximately 6 weeks).]

    Burnout will be assessed with the 12-item Burnout Assessment Tool (BAT; Schaufeli, De Witte, & Desart, 2020). 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."). Also, these scales are completed with two supplementary scales: psychological complaints (5 items; "I feel tense and stressed.") and psychosomatic complaints (5 items; "I suffer from headaches."). All items will be scored on a 5-point scale ranging from 1 (never) to 5 (always).

  2. Job satisfaction [Change from baseline to post-intervention (approximately 6 weeks).]

    Job satisfaction will be measured with the Michigan Organizational Assessment Questionnaire (Camman et al., 1979). 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.".

  3. Job performance [Change from baseline to post-intervention (approximately 6 weeks).]

    Job performance will be assessed with a 7-item scale developed by Williams and Anderson (1991). 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.".

  4. Positive affect [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, Watson et al., 1988; Crawford & Henry, 2004), 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).

  5. Life satisfaction [Change from baseline to post-intervention (approximately 6 weeks).]

    Life satisfaction will be measured with the five items of the Satisfaction with Life Scale developed by Diener et al. (1985). 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".

Other Outcome Measures

  1. Satisfaction with the intervention [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 (Tulbure et al., 2018). 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.

  2. System usability [At study completion (post-intervention), an average of 6 weeks.]

    We will use a 10-item questionnaire (Bangor et al., 2009) 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.

  3. Treatment adherence [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).

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 35 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • the eligible participants should have a maximum work experience of 3 years;

  • participants should score 4 or lower than 4 (on a scale from 0 to 6) on work engagement;

  • participants' job autonomy should permit bottom-up changes to their work routines (based on a filter Yes/No question);

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).

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • West University of Timisoara

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
West University of Timisoara
ClinicalTrials.gov Identifier:
NCT05474807
Other Study ID Numbers:
  • MEGSIS S3 Pilot
First Posted:
Jul 26, 2022
Last Update Posted:
Jul 26, 2022
Last Verified:
Jun 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by West University of Timisoara
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 26, 2022