- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06742047
A Professional Development Programme (ProDeveloP) for Newly Graduated Nurses
Implementing a Professional Development Programme (ProDeveloP): an Introduction for Newly Graduated Nurses
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The primary outcomes will be role clarity, task mastery, social acceptance, recovery and stress. The researchers will compare the results of the primary outcomes with those of a control group measure. Secondary outcomes will be experience of the intervention, transition support, job satisfaction and intention to leave.
Informed consent was signed prior to participation in the study. The ethical application has been approved by the Ethics Authority IS, diary number 2022-05682-0.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Västerås, Sweden, 721 23
- Mälardalens University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion criteria:
- Registered nurses in Sweden employed as Newly Graduated Nurses (NGNs) in a county in central Sweden participating in the ProDeveloP, the intervention group.
- Registered nurses in Sweden employed as Newly Graduated Nurses (NGNs) in a county in central Sweden, NGNs participating in the introduction programme prior to the study, not participating in the ProDeveloP, the control group.
- Experienced registered nurses as facilitators for the dialogue groups for the NGNs in the intervention.
- Managers at the county hospital for the NGNs participating in the intervention.
Exclusion criteria:
• Managers without NGNs participated in the intervention.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Participating in the Professional development program (ProDeveloP)
The group received the intervention of the Professional Development Programme (ProDeveloP).
The planning of the ProDeveloP has been done in close collaboration with stakeholders within the hospital setting where the programme will be implemented.
The programme includes face-to-face approaches from peer learning and e-learning modalities.
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The professional development programme include dialogue groups facilitated by registered nurses (RN) who are expert and experienced supervisors that received a three day training before conducting the groups.
Then including education days with joint lectures and simulations with experts in the field with experience.
The programme provides NGNs with regular opportunities for reflection for learning from experiences of care to enhance personal and professional growth.
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No Intervention: Control group prior the intervention in 2022
The group did not receive the intervention but participated in the prior introduction programme in 2022 including 8 educational days.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Role Clarity
Time Frame: The measurement was collected at one time point at thirteen weeks of participation in the ProDeveloP for the intervention group or in the prior introduction programme for the control group.
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Role clarity, the professional development process in terms of gaining clarity about the responsibilities content and boundaries of the role, was measured with the Validated scale from the Questionnaire for Psychological and Social Factors at Work (QPS Nordic). A 5-point Likert scale was used with three items. During the last week, how did you feel about:
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The measurement was collected at one time point at thirteen weeks of participation in the ProDeveloP for the intervention group or in the prior introduction programme for the control group.
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|
Task Mastery
Time Frame: The measurement was collected at one time point at thirteen weeks of participation in the ProDeveloP for the intervention group or in the prior introduction programme for the control group.
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Task mastery was measured with the validated scale from Swedish version of the Needs Satisfaction and Frustration Scale (NSFS). A 5-point Likert scale was used with two items.
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The measurement was collected at one time point at thirteen weeks of participation in the ProDeveloP for the intervention group or in the prior introduction programme for the control group.
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Social Acceptance
Time Frame: The measurement was collected at one time point at thirteen weeks of participation in the ProDeveloP for the intervention group or in the prior introduction programme for the control group.
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Social acceptance, of being integrated into the work group and belonging at work, was measured with the validated Needs Satisfaction and Frustration Scale (NSFS). A 5-point Likert scale was used with two items. During the last week: I have felt that the people I work with have really cared about me? I have felt included in the work group?A 5-point lickert scale was used. These items range from 'Very seldom or never (0)' to 'Very often or always' (4). The items were summed to between 0-8. Higher summed scores indicated better outcomes. |
The measurement was collected at one time point at thirteen weeks of participation in the ProDeveloP for the intervention group or in the prior introduction programme for the control group.
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Stress
Time Frame: The measurement was collected at one time point at thirteen weeks of participation in the ProDeveloP for the intervention group or in the prior introduction programme for the control group.
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Stress levels was measured with the validated Stress and Energy Questionnaire (SEQ). A 5-point Likert scale was used with three items. During the last week when you have been working, how often have you felt:
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The measurement was collected at one time point at thirteen weeks of participation in the ProDeveloP for the intervention group or in the prior introduction programme for the control group.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Job Satiscation
Time Frame: Measured during months 4, 8 and 12 after enrollment of the intervention. No control group measurements are available for the secondary outcomes.
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Job satisfaction was measrued validated Job Satisfaction scale with 5-point lickert scale with three items. How often do you feel about your work in the following ways
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Measured during months 4, 8 and 12 after enrollment of the intervention. No control group measurements are available for the secondary outcomes.
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Intentions to Leave
Time Frame: Measured during months 4, 8 and 12 after enrollment of the intervention. No control group measurements are available for the secondary outcomes.
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Intentions to leave the workplace or profession was measured by the validated Organizational Commitment on Job Turnover Intention scale. Please respond to the following statements about changing workplace:
Please comment on the following statements about changing profession:
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Measured during months 4, 8 and 12 after enrollment of the intervention. No control group measurements are available for the secondary outcomes.
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Recovery
Time Frame: Measured during months 4, 8 and 12 after enrollment of the intervention. No control group measurements are available for the secondary outcomes.
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Recovery was measured by the validated Karolinska Sleep Questionnaireith 5-point Likert scale ranging from "not at all" to "very much". The Sleep quality of 3 items from the subjective meaning of good sleep from: 1. Did you have trouble falling asleep last night? 2. How did you sleep last night? 3. Have you slept restlessly? 2 item of being able to let go of work thoughts
1. During the past week, have you been able to do activities that give you energy? |
Measured during months 4, 8 and 12 after enrollment of the intervention. No control group measurements are available for the secondary outcomes.
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Margareta Asp, Professor, Mälardalens University
Publications and helpful links
General Publications
- Lindblom M, Widarsson M, Sodersved Kallestedt ML, Letterstal A, Nilsson KW, Asp M, Hoglander J. Associations Between Participation in ProDeveloP and Newly Graduated Nurses' Stress and Professional Development When Transitioning into Practice. SAGE Open Nurs. 2026 Feb 9;12:23779608261421265. doi: 10.1177/23779608261421265. eCollection 2026 Jan-Dec.
- Lindblom M, Hoglander J, Letterstal A, Sodersved Kallestedt ML, Asp M, Widarsson M. Reflection Supports Newly Graduated Nurses' Professional Development When Transitioning Into Practice. J Clin Nurs. 2025 Jul;34(7):2948-2960. doi: 10.1111/jocn.17772. Epub 2025 Apr 10.
- Hoglander J, Lindblom M, Sodersved Kallestedt ML, Letterstal A, Asp M, Widarsson M. Implementing a Professional Development Programme (ProDeveloP) for Newly Graduated Nurses: A Study Protocol. Nurs Rep. 2025 Jul 2;15(7):243. doi: 10.3390/nursrep15070243.
Helpful Links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 220065
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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