Evaluation of MOTIV@Coeur, an e-learning method in motivational interviewing for nurses in cardiovascular care
ISRCTN | ISRCTN16510888 |
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DOI | https://doi.org/10.1186/ISRCTN16510888 |
Secondary identifying numbers | ICM-2015-1948 |
- Submission date
- 21/02/2016
- Registration date
- 22/02/2016
- Last edited
- 22/08/2016
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Circulatory System
Plain English summary of protocol
Background and study aims
Cardiovascular disease (CVD) is a general term used to describe a disease affecting the heart or blood vessels. It is becoming more and more widespread, and is a major cause of death worldwide. There is a great deal of evidence showing that changing healthy lifestyle choices, such as quitting smoking, eating a healthier diet and exercising more, can help to lower the risk of developing CVD and even reduce symptoms in existing sufferers. Many patients however can be reluctant to make lifestyle changes and so helping to motivate them is very important. Motivational interviewing (MI) is a technique which uses goal-oriented, individual counselling to help encourage changes in behaviour. Although it has been shown to be very effective, few nurses are trained in MI due to high costs and low availability of training. The MOTIV@Coeur website is a new e-learning training program that has been designed to train nurses in MI techniques. The aim of this study is to investigate the effectiveness and practicality of this program at training nurses who work in coronary (heart) care in MI techniques.
Who can participate?
Nurses who work in the coronary (heart) care unit of Montreal Heart Institute.
What does the study involve?
All participants are assigned an identification number that they can use to log in on the MOTIV@Coeur website to complete the online training sessions. At the start of the study, participants are given the choice as to whether they would like to complete the first session at the study centre or at home. The session takes around 30 minutes to complete and involves training in motivational interviewing in different hypothetical clinical situations. This is in the form of mole-modelling videos, in which a role model (cardiology nurse practitioner) evaluates a patient’s motivation to change their lifestyle for the benefit of their health (i.e. quitting smoking, improving diet, exercising more) and intervenes appropriately. Each of the clinical situations features patients with different levels of conviction and confidence towards changing their lifestyle. Participants then complete a second session at home around 15 days after the first session. After thirty days, participants complete a number of questionnaires and usage data is collected from the website in order to assess how well the MOTIV@Coeur program has been received and its effectiveness.
What are the possible benefits and risks of participating?
Participants will benefit from receiving training in motivational interviewing which they can include in their College of Registered Nurses of Quebec portfolio. There are no notable risks involved with taking part in this study.
Where is the study run from?
Montreal Heart Institute (Canada)
When is the study starting and how long is it expected to run for?
September 2014 to August 2016
Who is funding the study?
1. Canadian Institutes of Health Research (Canada)
2. Montreal Heart Institute’s Research Center (Canada)
3. Quebec’s Minister of Higher Education, Research and Science (Canada)
Who is the main contact?
1. Mr Guillaume Fontaine (public)
guillaume.fontaine@umontreal.ca
2. Dr Sylvie Cossette (scientific)
sylvie.cossette.inf@umontreal.ca
Contact information
Public
Montreal Heart Institute
5000, Belanger street
Montreal, Quebec
H1T1C8
Canada
0000-0002-7806-814X | |
Phone | +1 (0)514 3763330 Ext. 3069 |
guillaume.fontaine@umontreal.ca |
Scientific
Montreal Heart Institute
5000, Belanger street
Montreal, Quebec
H1T1C8
Canada
0000-0001-5840-9122 | |
Phone | +1 (0)514 376 3330 Ext. 4012 |
sylvie.cossette.inf@umontreal.ca |
Study information
Study design | Single-group pre-post pilot study |
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Primary study design | Interventional |
Secondary study design | Non randomised study |
Study setting(s) | Hospital |
Study type | Other |
Participant information sheet | Not available in web format, please use the contact details below to request a patient information sheet. |
Scientific title | Evaluation of MOTIV@Coeur, an E-learning Method in Motivational Interviewing for Nurses in Cardiovascular Care: a pilot study FRENCH: Évaluation de la méthode d’E-learning en entretien motivationnel MOTIV@Coeur auprès d’infirmières en soins cardiovasculaires: une étude pilote |
Study acronym | MOTIV@Coeur |
Study objectives | The aim of this study is to develop and assess the feasibility and acceptability of an E-learning method in motivational interviewing (MOTIV@Coeur) for cardiovascular nurses using a pre-post design. The secondary aims of this trial are to assess the preliminary effect of MOTIV@Coeur on nurses’ perceived skills in motivational interviewing as well as their frequency of delivering motivational interventions in the Coronary Care Unit. Hypotheses: Compared with the pre-training period, nurses trained with MOTIV@Coeur will present: 1. Higher perceived skills in motivational interviewing 2. More frequent delivery of motivational interventions for coronary patients |
Ethics approval(s) | Montreal Heart Institute Ethics Committee, 29/01/2016, ref: 15-1948 |
Health condition(s) or problem(s) studied | 1. Secondary prevention in cardiology 2. Training in motivational interviewing |
Intervention | Following provision of informed consent, nurses will be assigned an identification number with which they can identify themselves on the MOTIV@Coeur website to complete both MI training sessions online. During the first phase of the project, nurses will have to choose between completing the first session at the research setting in a computer lab or carrying out the first session of MOTIV@Coeur at home. In both cases, they will receive answers to their questions but won’t receive any explanations of theoretical concepts by the student researcher. Questions asked will be addressed and documented in a Word file for descriptive purposes. The second MOTIV@Coeur session, also about 30 minutes in duration, will be completed at home about 15 days (± 5 days) after the first session. If participants interrupt a session, they may resume where they left off, or return to the beginning. Data collection for outcome measures will occur at 30 days (± 5 days) following the completion of the first training session. The two questionnaires on the measurement results will be completed confidentially online with email and phone call reminders as needed. The experimental intervention (MOTIV@Coeur) is an E-learning method in motivational interviewing (MI) based on role-modeling videos. The intervention content is based on the work of several authors on brief motivational interventions. MOTIV@Coeur is available on the Web and consists of two sessions of 30 minutes each in which a theoretical introduction to MI is followed by two videos of plausible clinical situations on a coronary unit, in which a cardiology nurse practitioner (CNP) acts as a role model and then explains the interventions used. The clinical situations target secondary prevention with patients addressing lifestyle issues such as smoking, adherence to cardiovascular medications, physical activity or diet. In the videos, the CNP evaluates the patient's motivation to change and then intervenes according to the principles of brief motivational interviewing. Each of the clinical situations features patients with different levels of conviction and confidence towards changing their lifestyle. |
Intervention type | Other |
Primary outcome measure | Proportion of nurses completing the two training sessions is recorded using website usage data within 15 days (± 5 days). |
Secondary outcome measures | Feasibility outcomes: Feasibility of the MOTIV@Coeur intervention will be measured at 30 days (± 5 days) by recording: 1. The proportion of nurses who agree to participate in the study compared to the number in the target population 2. The time required for recruitment of participants 3. The proportion of nurses trained within the time frame suggested by the research team (time of use and time between sessions) 4. The proportion of nurses completing all outcome measures from baseline to 30 days (± 5 days) according to the research protocol Acceptability: The acceptability of MOTIV@Coeur for cardiovascular nurses will be measured at 30 days (± 5 days) using a survey designed to assess nurses’ opinions on 27 items in eight sub-dimensions of the E-learning method (i.e., system quality, quality of proposed information, quality of services associated with the system, quality of the user interface, perceived usefulness, perceived ease of use, perceived pleasure to use, and finally, intent to use). Perceived skills and motivational interventions: The perceived skills towards different motivational interventions and the perceived frequency of motivational interventions for coronary patients will be measured by a survey adapted from the list of Nursing Interventions for different levels of conviction and confidence at 30 days (± 5 days). Other: The use of MOTIV@Coeur (number of completed sessions (1 or 2)), time using the application (minutes) and subsequent use of the application (or not) will be recorded using website usage data at 30 days (± 5 days). |
Overall study start date | 01/09/2014 |
Completion date | 13/05/2016 |
Eligibility
Participant type(s) | Health professional |
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Age group | Adult |
Sex | Both |
Target number of participants | 30 participants. |
Key inclusion criteria | 1. Certification from the Order of Nurses of Quebec or Candidate for the Exercise of Nursing Profession (people who have completed their college or university nursing programs and have a restricted practice, but are waiting for their full license to practice nursing) 2. Full-time position or replacement shift in the coronary care unit 3. Comfort with basic computer instructions |
Key exclusion criteria | Those who have undertaken training in motivational interviewing in the past year |
Date of first enrolment | 07/03/2016 |
Date of final enrolment | 07/04/2016 |
Locations
Countries of recruitment
- Canada
Study participating centre
Montreal
H1T1C8
Canada
Sponsor information
Hospital/treatment centre
5000, Belanger street
Montreal
H1T1C8
Canada
https://ror.org/03vs03g62 |
Funders
Funder type
Government
Government organisation / National government
- Alternative name(s)
- Instituts de Recherche en Santé du Canada, Canadian Institutes of Health Research (CIHR), CIHR_IRSC, Canadian Institutes of Health Research | Ottawa ON, CIHR, IRSC
- Location
- Canada
No information available
No information available
Results and Publications
Intention to publish date | 30/09/2016 |
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Individual participant data (IPD) Intention to share | No |
IPD sharing plan summary | Not expected to be made available |
Publication and dissemination plan | Planned publication of study results in the Journal of Medical Internet Research. |
IPD sharing plan |
Study outputs
Output type | Details | Date created | Date added | Peer reviewed? | Patient-facing? |
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Results article | results | 18/08/2016 | Yes | No |
Editorial Notes
22/08/2016: Publication reference added.
31/05/2016: The overall trial end date was changed from 31/08/2016 to 13/05/2016.
23/02/2016: Verified study status with principal investigator.