- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05335759
Coaching Programme for Preceptorship of Undergraduate Nurses' Students
Coaching Programme to Improve Nurses' Perceptions of Preceptorship of Undergraduate Students: An Exploratory Trial
Background: During the curricular practices of the Bachelor's Degree in Nursing, students are prepared to carry out an adequate transition process to the professional role. The success of this preparation depends, to a large extent, on preceptorship. In this sense, it is important that practice tutors are motivated and feel competent to teach in the clinical setting. Despite this, no studies have been found that implement and evaluate an intervention to improve nurses' perceptions of preceptorship of undergraduate nursing students.
Purpose: To evaluate the preliminary efficacy of a coaching programme to improve nurses' perceptions of preceptorship of undergraduate nursing students. Specifically, the aim is to determine the impact of the programme on nurses' perceived involvement, motivation, satisfaction, barriers and commitment to clinical mentoring.
Method: An exploratory pre-post quasi-experimental pilot study. Fifteen nurses, the total population of nurses working in the medical-surgical ward, with at least 1 year of experience in the preceptorship of students, will be recruited in June 2022. All the nurses will receive an intervention based on coaching. The strategies of this program consisted of five 6-hour sessions using case studies and role-playing simulations to work on their motivation to develop their teaching role in the preceptorship of undergraduate nursing students and debriefing and a 4-hour booster session seven months later. The IMSOC (involvement, motivation, satisfaction, obstacles and commitment) instrument was used to assess outcomes. The primary outcome was the difference in the median of nurses' involvement, motivation, satisfaction, barriers and commitment in preceptorship students pre and post-intervention (between T0-T1 and T0-T2). Changes within nurses were analyzed using the Wilcoxon test for related samples.
Study Overview
Status
Intervention / Treatment
Detailed Description
Data collection:
Data collection was divided into three times: T0, T1 and T2. T0 corresponds to preintervention data and T1 and T2 to post-intervention data (T1 after the training and T2 after the whole intervention implementation).
IMSOC (Involvement, Motivation, Satisfaction, Obstacles and Commitment) questionnaire. This questionnaire measures the involvement, motivation, satisfaction, obstacles and commitment of nurses in tutoring students. It is a validated instrument that shows adequate psychometric properties (overall Intraclass Correlation Coefficient (ICC) of 0.852 and internal consistency - Cronbach's α of 0.837). It consists of 33 items measured on a 5-point Likert scale (1=strongly disagree - 5=strongly agree).
Ethical considerations:
This study conformed to the principles set out in the Declaration of Helsinki and was approved by the centre's board and by the Research Ethics Committee (code 2022.044). Data custody complied with Organic Law 3/2018 on data protection (LOPDE). Informed consents were given to all participants. They were informed verbally and in writing about their free participation, the confidentiality of the data and its use for scientific purposes.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
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Pamplona, Spain
- University of Navarra
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Pamplona, Spain, 31008
- Navarre
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Nurses working in the medical-surgical ward.
- Nurses with at least one year's experience in the preceptorship of students.
- Nurses who have voluntarily agreed to participate in the study.
Exclusion Criteria:
- Nurses who are not working during the time of the study (sick leave or maternity leave).
Study Plan
How is the study designed?
Design Details
- Observational Models: Other
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
IMSOC (Involvement, Motivation, Satisfaction, Obstacles and Commitment) Questionnaire
Time Frame: T0 (2022 September-October)
|
Nurses' involvement, motivation, satisfaction, barriers and commitment in preceptorship students Measurement tool: IMSOC (Involvement, Motivation, Satisfaction, Obstacles and Commitment) Questionnaire.
|
T0 (2022 September-October)
|
|
IMSOC (Involvement, Motivation, Satisfaction, Obstacles and Commitment) Questionnaire
Time Frame: T1 (2022 November)
|
Nurses' involvement, motivation, satisfaction, barriers and commitment in preceptorship students Measurement tool: IMSOC (Involvement, Motivation, Satisfaction, Obstacles and Commitment) Questionnaire.
|
T1 (2022 November)
|
|
IMSOC (Involvement, Motivation, Satisfaction, Obstacles and Commitment) Questionnaire
Time Frame: T2 (2023 May)
|
Nurses' involvement, motivation, satisfaction, barriers and commitment in preceptorship students Measurement tool: IMSOC (Involvement, Motivation, Satisfaction, Obstacles and Commitment) Questionnaire.
|
T2 (2023 May)
|
Collaborators and Investigators
Investigators
- Principal Investigator: Mónica Vázquez-Calatayud, PhD, University of Navarra
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 (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- CPMS
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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