IJobs - an Internet Intervention for the Unemployed (iJobs)

March 26, 2025 updated by: West University of Timisoara

IJobs - an Internet Intervention for the Unemployed: a Randomized Controlled Trial

The current study aims to test the efficacy of iJobs, an online intervention for the unemployed. iJobs is an online adaptation of the JOBS program.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

The current study is a two-arm randomized controlled trial that will test the efficacy of iJobs (a web-based adaptation of the JOBS program) against a waiting list control group. Participants from the control group will be enrolled in iJobs 2 weeks after the experimental group finishes the program. iJobs is a 2-week intervention consisting of 5 modules focusing on discovering job skills, job search strategies, preparing effective resumes, exercising different types of interviews, and overcoming setbacks in the job search process. iJobs was previously tested in a feasibility and acceptability trial.

Study Type

Interventional

Enrollment (Actual)

176

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

      • Timişoara, Romania, 300223
        • West University of Timișoara

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

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Unemployed and looking for a job
  • Work as volunteers and are looking for a paid job
  • Have a PC or laptop and basic digital competencies

Exclusion Criteria:

  • They don't have internet access and are not available during the two weeks of the program

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: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Intervention group
The group that will be first randomly allocated to iJobs.
iJobs is a 2-week intervention consisting of 5 modules focusing on discovering job skills, job search strategies, preparing effective resumes, exercising different types of interviews, and overcoming setbacks in the job search process. This is an adaptation of the JOBS program.
Experimental: Waiting list control group
This group will receive the intervention 2-weeks after the intervention group finishes it.
iJobs is a 2-week intervention consisting of 5 modules focusing on discovering job skills, job search strategies, preparing effective resumes, exercising different types of interviews, and overcoming setbacks in the job search process. This is an adaptation of the JOBS program.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Participants' self-efficacy regarding the job search process
Time Frame: Change from baseline to post-intervention and follow-up (approximately 2 weeks and 6 weeks)
The Job Search Self-Efficacy Scale (20-item) measures participants' perception of their ability to gain employment. The minimum score is 20 and the maximum is 100. A higher score means a better outcome (increased job search self-efficacy).
Change from baseline to post-intervention and follow-up (approximately 2 weeks and 6 weeks)
Participants' job search intensity and effort
Time Frame: Change from baseline to post-intervention and follow-up (approximately 2 weeks and 6 weeks)
The investigators will use a version of Blau's Job-search behaviors scale adapted to the contemporary context and Romanian population. The scale measures participants' involvement in job search activities in terms of frequency and intensity. The minimum score is 16 and the maximum is 80. A higher score means a better outcome (increased job search behavior effort).
Change from baseline to post-intervention and follow-up (approximately 2 weeks and 6 weeks)
The quality of participants' job search behaviors
Time Frame: Change from baseline to post-intervention and follow-up (approximately 2 weeks and 6 weeks)
The Job search quality scale has 20 items and measures the quality in which the job search behaviors are performed. The minimum score is 20 and the maximum is 100. A higher score means a better outcome (increased job search quality).
Change from baseline to post-intervention and follow-up (approximately 2 weeks and 6 weeks)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Participants' ability to deal with setbacks in the job search process
Time Frame: Change from baseline to post-intervention (approximately 2 weeks)
Inoculation against setbacks (i.e., participants' ability to deal with setbacks) will be measured using 2 items retrieved from previous studies. The minimum score is 2 and the maximum is 10. A higher score means a better outcome (presence of inoculation against setbacks).
Change from baseline to post-intervention (approximately 2 weeks)
Participants' overall self-esteem
Time Frame: Change from baseline to post-intervention (approximately 2 weeks)
Rosenberg's Self Esteem Scale measures global self-worth by measuring both positive and negative feelings about the self using 10 items. The minimum score of Rosenberg's Self Esteem Scale is 10 and the highest one is 40. A higher score means a better outcome.
Change from baseline to post-intervention (approximately 2 weeks)
Participants' anxiety regarding their future career
Time Frame: Change from baseline to post-intervention (approximately 2 weeks)
The investigators will measure participants' anxiety regarding their future career with the Future Career Anxiety Scale. The minimum score is 5 and the maximum is 25. A higher score means a worse outcome (increased anxiety).
Change from baseline to post-intervention (approximately 2 weeks)
Generalised Anxiety symptoms
Time Frame: Change from baseline to post-intervention (approximately 2 weeks)
The investigators will measure participants' anxiety symptoms using the Generalised Anxiety Disorder Assessment. This is a 7-item instrument that uses the DSM-V criteria to assess anxiety symptom severity. The minimum score is 0 and the highest one is 21. A higher score means a worse outcome (a higher level of anxiety).
Change from baseline to post-intervention (approximately 2 weeks)
Depression symptoms
Time Frame: Change from baseline to post-intervention (approximately 2 weeks)
The investigators will measure participants' depression symptoms with the Patient Health Questionnaire-9. The scale measures participants' severity of depression using DSM IV criteria. The minimum score is 0 and the highest one is 27. A higher score means a worse outcome (more severe symptoms of depression).
Change from baseline to post-intervention (approximately 2 weeks)
Participants' mental health complaints
Time Frame: Change from baseline to post-intervention (approximately 2 weeks)
The investigators will measure participants' mental health complaints with the Mental Health Complaints Scale. This is a 5-item instrument that will be used to assess mental health complaints. The minimum score is 6 and the highest is 30. A higher score means a worse outcome.
Change from baseline to post-intervention (approximately 2 weeks)
Participants' psychological capital
Time Frame: Change from baseline to post-intervention (approximately 2 weeks)
The investigators will measure participants' psychological capital with the 12-item Compound PsyCap Scale. The minimum score is 12 and the highest is 72. A higher score means a better outcome.
Change from baseline to post-intervention (approximately 2 weeks)

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Physical health
Time Frame: Baseline only
The investigators will use a short version of Ware's Physical Health Complaints Scale to measure participants' perceptions of their health. The minimum score is 4 and the highest is 20. A higher score means a worse outcome (worse physical health).
Baseline only
Treatment adherence
Time Frame: Post-intervention only (approximately 2 weeks)
Drop out rate; 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).
Post-intervention only (approximately 2 weeks)
Satisfaction with the intervention
Time Frame: Post-intervention only (approximately 2 weeks)
Satisfaction with the intervention will be measured using 17 items. Eleven items are measured on a 4-points, 5-points, and 10-points Likert scale. Each item will be analyzed separately. A higher score means greater satisfaction. The other 6 items are open-ended questions and imply qualitative analysis.
Post-intervention only (approximately 2 weeks)
System usability
Time Frame: Post-intervention only (approximately 2 weeks)
We will use a 10-item questionnaire designed to measure participants' satisfaction with TalentLMS, the online platform used for the program delivery. The total score of System Usability Scale is 0 and the highest one is 100. A higher score means a better outcome.
Post-intervention only (approximately 2 weeks)
Sociodemographic information
Time Frame: Baseline only
Age, gender, residential area, educational level, average monthly income, unemployment period, work experience, and targeted professional field.
Baseline only
Employment status
Time Frame: Follow-up only (approximately 6 weeks)
Self-reported employment status will be measured at follow-up, using a dichotomous question.
Follow-up only (approximately 6 weeks)
Employment satisfaction
Time Frame: Follow-up only (approximately 6 weeks)
Self-reported employment quality will be measured at follow-up using 4 questions. One of them is a dichotomous question, while the other 3 questions are measured on a Likert scale. The minimum score is 3, and the maximum is 30. A higher score means greater satisfaction with the job.
Follow-up only (approximately 6 weeks)

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Andrei Rusu, West University of Timișoara

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)

June 6, 2023

Primary Completion (Actual)

October 2, 2024

Study Completion (Actual)

November 2, 2024

Study Registration Dates

First Submitted

June 19, 2023

First Submitted That Met QC Criteria

July 24, 2023

First Posted (Actual)

July 27, 2023

Study Record Updates

Last Update Posted (Actual)

April 2, 2025

Last Update Submitted That Met QC Criteria

March 26, 2025

Last Verified

November 1, 2024

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • RCT iJobs

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

product manufactured in and exported from the U.S.

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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