Feasibility and Acceptability of the Online JOBS Program (iJobs)

March 9, 2023 updated by: West University of Timisoara

iJobs - Testing the Feasibility and Acceptability of an Online Adaptation of the Jobs Program: an Open-label Pilot Study

The aim of this study is to test the feasibility and acceptability of a web-based adaptation of the Jobs program (developed by Curran et al., 1999).

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

The current study is an open trial that will test the feasibility and acceptability of a web-based adaptation of the Jobs program (further be referred to as iJobs). We will use a repeated measures design: one group and three measurements (baseline, post-intervention, 3 months follow-up). iJobs consists of five sessions spread over a two-week period. The participants will learn and exercise successful job search strategies (e.g. finding job openings, creating an attractive resume, demonstrating effective interviews).

Study Type

Interventional

Enrollment (Actual)

56

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 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

18 years to 60 years (Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Unemployed and looking for a job
  • Work as volunteers and 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
  • Suffer from a chronic disease that implies special conditions for taking part in the activities
  • Severe clinical depression symptoms (Cut-off=15 at PHQ9)*
  • Severe clinical anxiety symptoms (Cut-off=15 at GAD7)*

(*) will be included if they receive mental health treatment

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: iJobs
All the participants will be included in the program.
During the program, the participants will learn and exercise successful job search strategies. The web-based adaptation of the Jobs program will allow self-administration. After each session, they will receive written feedback from trainers on the platform.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Job search behavior effort
Time Frame: Change from baseline to follow-up (3 months).
Job search behavior effort: Job Search Behavior Scale (Blau, 1994) was designed to measure 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 follow-up (3 months).
Satisfaction with the intervention
Time Frame: Post-intervention (2 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 in a face-to-face JOBS intervention. 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 delivered on the same platform as we will use for our program. 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 and imply qualitative analysis.
Post-intervention (2 weeks).
System usability
Time Frame: Post-intervention (2 weeks).
We will use a 10 item questionnaire (Bangor et al., 2009) designed to measure participants' satisfaction with e-cbt, 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 (2 weeks).
Treatment adherence
Time Frame: Post-intervention only (2 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).
Post-intervention only (2 weeks).

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Job-Search Self-Efficacy
Time Frame: Change from baseline to post-intervention (2 weeks).
Job Search Self-Efficacy Scale was designed to measure participants' perception of their ability to gain employment. We will use the 20 item version of the scale developed by Saks et al., 2015. 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 (2 weeks).
Self-esteem
Time Frame: Change from baseline to post-intervention (2 weeks).
Rosenberg's Self Esteem Scale is a self-esteem measure widely used in social science research. It is a ten-item Likert-type scale with items answered on a four-point scale-from strongly disagree to strongly agree. The scale measures global self-worth by measuring both positive and negative feelings about the self. 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 (2 weeks).
Inoculation against setbacks
Time Frame: Change from baseline to post-intervention (2 weeks).
We will use 2 items retrieved from previous studies (Vuori & Vinokur, 2005) aiming to measure the effectiveness of JOBS intervention in terms of participant's ability to deal with setbacks. 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 (2 weeks).
Future Career Anxiety
Time Frame: Change from baseline to post-intervention (2 weeks).
We will measure participant's anxiety regarding their future career in the context of the COVID-19 outbreak with the Future Career Anxiety Scale developed by Tsai et al., 2017 (Mahmud et al., 2020). 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 (2 weeks).
Patient Health Questionnaire-9 (PHQ9)
Time Frame: Change from baseline to post-intervention (2 weeks).
Patient Health Questionnaire-9 was designed to measure participants' severity of depression using DSM IV criteria. The minimum score of Patient Health Questionnaire-9 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 (2 weeks).
Generalised Anxiety Disorder Assessment (GAD7)
Time Frame: Change from baseline to post-intervention (2 weeks).
Generalised Anxiety Disorder Assessment is a self-administered 7 item instrument that uses some of the DSM-V criteria for GAD (General Anxiety Disorder) to identify probable cases of GAD along with measuring anxiety symptom severity. The minimum score of Generalised Anxiety Disorder Assessment 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 (2 weeks).
Employment status
Time Frame: Follow-up (3 months).
Self-reported employment status (phone screening).
Follow-up (3 months).
Job Quality
Time Frame: Follow-up (3 months).
For those who found employment - phone screening.
Follow-up (3 months).

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Physical health
Time Frame: Baseline only (factors to be controlled for).
We will use a short-version of the Physical Health Complaints Scale (Ware, 1999) to measure participants' perception 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 (factors to be controlled for).
Financial strain
Time Frame: Baseline only (factors to be controlled for).
We will use a single item from Vuori & Vinokur, 2005 to assess participants' financial strain, respectively: 'What is the financial situation of your family/household in your opinion?'. The minimum score is 1 while the maximum is 5. A higher score means a high level of financial strain.
Baseline only (factors to be controlled for).
Sociodemographic information
Time Frame: Baseline only
Age, gender, background, educational level, average monthly income, unemployment period, work experience, and targeted professional field.
Baseline only

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)

May 24, 2021

Primary Completion (Actual)

October 10, 2021

Study Completion (Actual)

February 28, 2022

Study Registration Dates

First Submitted

April 28, 2021

First Submitted That Met QC Criteria

May 12, 2021

First Posted (Actual)

May 13, 2021

Study Record Updates

Last Update Posted (Actual)

March 14, 2023

Last Update Submitted That Met QC Criteria

March 9, 2023

Last Verified

April 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • iJobs

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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