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Building Your Successful Nursing Career

Building Your Successful Nursing Career: Evaluating the Effectiveness of a Career Planning Mobile Application for Male Nurses - a Randomized Double-blind Controlled Trial

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06519643
Enrollment
120
Registered
2024-07-25
Start date
2024-08-01
Completion date
2027-08-05
Last updated
2024-07-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gender, Nurse's Role, Professional Burnout

Keywords

male nurse, career plan, mobile application (App), intervention study, randomized controlled trial

Brief summary

This study aims to evaluate a career planning mobile App specifically tailored for male nurses.This three-year experimental project aims to recruit 120 male nurses (60)in the experimental group and 60 in the control group). Employing a prospective double-blind randomized controlled trial (RCT) design, the study will include six follow-up points (pre-intervention, post-intervention at 0, 6, 12, 18, and 24 months) to examine the effectiveness of career self-efficacy, career adaptive behaviors, occupational resilience, career success, and career continuity intentions of male nurses over time. The repeated measures data will be analyzed with the intention-to-treat analysis method and General Estimating Equations (GEE). This research represents an innovative development of the world's first theoretically grounded career planning mobile App for male nurses.The study's results can serve as a valuable reference for future career planning initiatives in nursing practice and education.

Detailed description

This study is a longitudinal study that adopts a double-blind randomized controlled trial (RCT). The study will recruit 120 male nurses and allocate them into the intervention group and the control group in a 1:1 ratio (60 in each group). Based on Super's (1957) career development theory and the four-stage career classification, the participating male nurses will be divided into the exploration stage (experience ≤ 2 years), establishment stage (experience 2-5 years), and maintenance stage (experience 5-15 years), with career stage as a confounding factor. The study uses 1:1:1 stratified randomization to ensure that the number of cases in the experimental group (n=60, exploration stage: establishment stage: maintenance stage = 20:20:20) and the control group (n=60) is the same, as well as the homogeneity of the career stage variables of the two groups. All included subjects will undergo an online pre-test (T0) before allocation, and then enter the experimental group or the control group according to the random assignment results. Both groups will be invited to use the Building Your Successful Nursing Career App for six months, with the experimental group receiving the full career planning mobile application intervention and two online Career Mentoring Programs, while the control group receives a sham treatment. Both groups will undergo five follow-up online data collections (0, 6, 12, 18, and 24 month post-intervention). The effectiveness of the career planning mobile application intervention on male nurses' career self-efficacy, career adaptive behaviors, occupational resilience, career success, and career continuity intentions will be examined using the intention-to-treat analysis method and General Estimating Equations (GEE).

Interventions

BEHAVIORALcareer planning application

Arm 1 \[Experimental group\]: The experimental group will be assigned to participate in a career planning application named Building Your Successful Nursing Career App for six months. They will receive the full career planning mobile application intervention along with two online career mentoring sessions. Arm 2 \[Control group\]: The control group will also be assigned to participate in a career planning application named Building Your Successful Nursing Career App for six months. However, the control group will only receive a sham treatment. They will only access a few interfaces of the app.

Sponsors

Chang Gung University
CollaboratorOTHER
Chang Gung Memorial Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Intervention model description

The investigators will compare the pre- and post-test differences between the experimental group and the control group. Both the experimental and control groups will fill in the structured questionnaires online at the time before the intervention (Baseline data) and at 0, 6, 12, 18, and 24 months after the intervention.

Eligibility

Sex/Gender
MALE
Healthy volunteers
Yes

Inclusion criteria

1. Male nursing staff currently engaged in clinical nursing work. 2. Care Within 15 years of working experience. 3. Have a mobile phone with Internet access. 4. Have clear consciousness and can understand and answer the researcher's questions. 5. Audible and understandable Or understand Chinese. 6. Willing to participate in this study and sign the subject consent form.

Exclusion criteria

1. Unwilling to participate in this study. 2. Those who cannot download the App.

Design outcomes

Primary

MeasureTime frameDescription
career self-efficacybefore intervention and 0, 6, 12, 18, and 24 months post-interventioncareer self-efficacy will be collected by online structure questionnaire
career adaptive behaviorsbefore intervention and 0, 6, 12, 18, and 24 months post-interventioncareer adaptive behavior will be collected by online structure questionnaire
occupational resiliencebefore intervention and 0, 6, 12, 18, and 24 months post-interventionoccupational resilience will be collected by online structure questionnaire
career successbefore intervention and 0, 6, 12, 18, and 24 months post-interventioncareer success will be collected by online structure questionnaire
career continuity intentionsbefore intervention and 0, 6, 12, 18, and 24 months post-interventioncareer continuity intentions will be collected by online structure questionnaire

Contacts

Primary ContactYu Hsing-Yi, PhD
kanano@gmail.com886-3-2118800

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026