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Nurse's Rolee-CPDNCT06047652

Development of Electronic Continuing Professional Development for Indonesian Clinical Nurses

A study testing e-CPD user testing in people with Nurse's Role, run by Universitas Muhammadiyah Yogyakarta.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

The goal of this clinical trial is to test a e-CPD prototype device for feasibility as it is applied within the clinical nursing setting in Level II clinical nurses in Indonesia. Read more about this study

Who is it for?
Any age
Conditions the study is for
Nurse's Role
What is being tested?
e-CPD user testing
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
7 participants
Where
No sites listed yet
Study dates
Sep 2023to Dec 2023
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Who may be able to join

  • Level I clinical nurses who works in hospital
  • Have a mobile device
  • Willing to take e-CPD user testing

Who cannot join

  • Did not complete the user testing

Trial locations and contacts

No sites are listed yet.

Novita K Sari, Master contact

+6281328066086

novita.kurniasari@umy.ac.id

About this study

Official title: Electronic Continuing Professional Development (e-CPD) Implementation, Process, and Outcomes for Indonesian Clinical Nurses: An Exploratory Action Research Study Protocol.

The goal of this clinical trial is to test a e-CPD prototype device for feasibility as it is applied within the clinical nursing setting in Level II clinical nurses in Indonesia. The main questions it aims to answer are:

  • What are the user needs for clinical nurse e-CDP development?
  • How is an instructional design developed for the development of e-CPD for clinical nurses?
  • What is the most suitable e-CPD format for clinical nurses?
  • How is the feasibility of e-CPD prototype?
Read the detailed description

This research is an exploratory action research. This design is principally exploratory research (plan to explore - explore - analyse, and reflect) followed by action research (plan to change - act - observe - reflect)

  1. Exploration This stage includes the plan to explore stage or stage 1 of 7 research stages. This stage prepares before collecting data. Researchers will start by building good interpersonal relationships with participants and the research environment. A good relationship can also create trust to improve the quality of the data collected. At this stage, researchers also compiled interview guidelines for 3 groups of participants. The next stage is exploring, which is stage 2 of the 7 stages of existing research. This stage conducts data collection through FGD to 3 groups of participants. The explanation of the implementation of the FGD is as follows: FGD on nurses will be conducted on 8-10 nurses who have performed CPD and have followed the credentials carried out by the hospital. The purpose of this FGD with nurses is to explore understanding, experience, obstacles, efforts made to overcome obstacles, and expectations on the implementation of CPD. FGD on hospital management will be conducted on 8-10 hospital managers who had a role in the implementation of nurse CPD. The interview explores hospitals' management, policies, barriers, and efforts in implementing nurse CPD. Interviews with hospital management were conducted simultaneously at almost the same time as the nurse's FGD. FGD on the Indonesian Nurses Association committee will be conducted on 8-10 committee members who have direct authority in the implementation of CPD. The FGD focuses on the policies, barriers, and efforts that professional organizations make on nurse CPD. The analysis and reflect stage or stage 3 of the 7 stages of this research will be carried out by analysing the results of the FGD. These results will used as a basis for determining strategic issues and potential solutions to the problems in this study. The interview will be conducted by 2 people, namely researchers and research assistants. Verbatim transcripts will be performed immediately after the interview is conducted by research assistants who follow the course of the interview.
  2. Action

This stage will begin with the plan to change, the 4th stage of 7 stages of research. This stage aims to draw up an instructional design that will form the basis for the development of the e-CPD system. Activities will be carried out with a series of workshops 2 times to get mutual agreement. The workshop will be attended by nurse managers, The Indonesian Nurses Association representatives, clinical nurse assessors, and nurses in charge of care. The results of stage 4 will produce the Clinical Nurse II Competency Training Curriculum. At this stage, an expert review is also carried out to assess the suitability of the module preparation with existing provisions. Expert reviews will also be conducted to ensure that the curriculum has met the established rules. At this stage, researchers identify the ability of clinical nurses as the primary users, required features, learning media, assignments and assessments set.

The next stage is act, which is stage 5 of the 7 stages of research. This stage will carried out through the development of the e-CPD system. Researchers, in collaboration with IT professionals, will develop an e-CPD system designed to be able to facilitate the learning process as well as evaluation according to the curriculum that has been compiled. At this stage, the e-CPD system is also reviewed by the same experts who provide curriculum reviews. This is done so that the e-CPD system is built in accordance with the curriculum that has been prepared.

The observation stage, stage 6 of the 7 existing research stages, will carry out user testing. User testing aims to test the functionality of the e-CPD design that has been developed. User testing was carried out on 10 nurses who will become users of this system with the criteria: level I clinical nurses who work in hospitals, have gadgets and are willing to participate in the e-CPD system trial. The instruments used use the System Usability Scale (SUS). Participants will be asked to access and try all the features of the e-CPD application. Then, participants will be asked to complete an SUS questionnaire containing 10 questions through Google Forms. This questionnaire contains ease of access and possible use for these participants.

Reflect stage, is the last stage, stage 7 of the 7. At this stage, analysis and evaluation of the entire study that has been carried out and determine follow-up.

Conditions
Nurse's Role
Being tested
e-CPD user testing
Keywords
exploratory action research, electronic learning, continuing professional development, protocol, nurse

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • e-CPD user testingDevice

    nurses who meet the criteria will carry out user testing on the e-CPD application via a mobile device. after accessing the e-CPD system the nurse will fill in the System Usability Scale instrument.

Study groups in NCT06047652
Study groupRoleWhat they receive
Intervention groupExperimentalThe e-CPD device will be given to the participant group according to the criteria. Each participant is given access rights for 1 week to try all the features in e-CPD.
Receives: Device: e-CPD user testing

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. evaluating usability of e-CPD system, using System Usability Scale (SUS) instrumen, and Data will be collected using a Google form link given to participants after trying all the features in the e-CPD system.

    SUS has 10 questions and 5 answer choices. Answer choices range from strongly disagree to strongly agree. SUS has a minimum score of 0 and a maximum score of 100.

    After the calculation is carried out, the assessment results will be obtained. SUS assessment guidelines are as follow the acceptable score is approximately above 70 (above our average of 68), and the unacceptable score is below 50 (closely corresponding to our classification of scores below 51.6). They evaluated the range between 50 and 70 to be "marginally acceptable,"

    Measured: Through study completion, an average of 3 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted21 Sep 2023
  2. Study startSep 2023 (estimated)
  3. Primary completionNov 2023 (estimated)
  4. Study completionDec 2023 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Device feasibility
Allocation
Not applicable
Intervention model
Single group
Model description
This study is a seven-stage exploratory action research, with stage 6 being the Moodle e-CPD trial for hospital nurses.
Masking
None (open label)
Enrolment
7 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06047652
Sponsor's protocol ID
e-CPD dev
Acronym
e-CPD
Status last verified
Sep 2023
First submitted
25 Aug 2023
Last updated
21 Sep 2023
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing e-CPD user testing in people with Nurse's Role, run by Universitas Muhammadiyah Yogyakarta.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 21 Sep 2023. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Novita K Sari, Master (+6281328066086, novita.kurniasari@umy.ac.id), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

evaluating usability of e-CPD system, using System Usability Scale (SUS) instrumen, and Data will be collected using a Google form link given to participants after trying all the features in the e-CPD system. (time frame: Through study completion, an average of 3 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 21 Sep 2023.

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