It is known that preeclampsia is a risk factor for cardiovascular diseases, diabetes, chronic hypertension, nephropathy and thromboembolism. The study's aim, subsequent to these informations, is to help prevent those consequences. Information tools have been known to enhance retention of information given orally. The objective of this study is to assess the knowledge and satisfaction of women after an episode of preeclampsia after reading an explanatory pamphlet on preeclampsia. The investigators also want to change their perception on cardiovascular risk, their risk of recurrence and preeclampsia's medium to long-term consequences and the ways to prevent them.
This is a randomised-controlled trial. Women recruted will first answer a questionnaire assessing demographic data, knowledge about risks in the future, perception of cardiovascular risk, anxiety about that risk and satisfaction about information received or collected. Then, women in the intervention group will receive the pamphlet. One month after, women in both groups will receive a questionnaire similar to the first one assessing knowledge about risks in the future, perception of cardiovascular risk, anxiety about that risk and satisfaction about information received or collected, including the pamphlet for the intervention group. The pamphlet was validated by a multidisciplany team including patients, doctors, nurses, education specialists and communication specialists. The questionnaire was also validated by the same multidisciplinary team. Section on knowledge and anxiety were remodeled from previously validated questionnaires Section on perception of cardiovascular risk was reproduced and translated with permission from its author. Section on satisfaction was reproduced from the investigators' previous study where it was validated.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Enrollment
90
The intervention group receives the information pamphlet
Centre Hopitalier Universiatire de Sherbrooke
Sherbrooke, Quebec, Canada
knowledge improvement (questionnaire with check list and true/false questions).
The primary outcome will be the comparison of knowledge between the intervention (with the pamphlet) and the control (without the pamphlet) group at one month with a validated questionnaire (knowledge: check list and true/false questions).
Time frame: 4 weeks
Perception of cardiovascular risk between the intervention and the control group at one month (Likert scale)
The comparison of perception of cardiovascular risk at one month between the intervention (with the pamphlet) and the control (without the pamphlet) group with a validated Likert scale included in the questionnaire.
Time frame: 4 weeks
Anxiety between the intervention and the control group at one month.(Likert scale)
Comparison of anxiety at one month between the intervention and the control group with a validated Likert scale included in the questionnaire.
Time frame: 4 weeks
Satisfaction between the intervention and the control group at one month.(Likert scale)
Comparison of satisfaction about all sources of information at one month between the intervention and the control group with a validated Likert scale included in the questionnaire.
Time frame: 4 weeks
Perception of cardiovascular risk in the intervention group between baseline and at one month (Likert scale)
The comparison of perception of cardiovascular risk between baseline and at one month in the intervention group with a validated Likert scale included in the questionnaire.
Time frame: 4 weeks
Perception of cardiovascular risk between baseline and at one month in the control group. (Likert scale)
The comparison of perception of cardiovascular risk between baseline and at one month in the control group with a validated Likert scale included in the questionnaire.
Time frame: 4 weeks
Anxiety in the intervention group between baseline and at one month (Likert scale)
The comparison of anxiety between baseline and at one month in the intervention group with a validated Likert scale included in the questionnaire.
Time frame: 4 weeks
Anxiety in the control group between baseline and at one month (Likert scale)
The comparison of anxiety between baseline and at one month in the control group with a validated Likert scale included in the questionnaire
Time frame: 4 weeks
Satisfaction in the intervention group between baseline and at one month(Likert scale)
The comparison of satisfaction between baseline and at one month in the intervention group with a validated Likert scale included in the questionnaire.
Time frame: 4 weeks
Satisfaction in the control group between baseline and at one month (Likert scale)
The comparison of satisfaction between baseline and at one month in the control group with a validated Likert scale included in the questionnaire.
Time frame: 4 weeks
Knowledge in the intervention group between baseline and at one month (questionnaire with check list and true/false questions).
The comparison of baseline knowledge and knowledge at one month in the intervention group with a validated questionnaire (knowledge: check list and true/false questions).
Time frame: 4 weeks
Knowledge in the control group between baseline and at one month (questionnaire with check list and true/false questions).
The comparison of Baseline knowledge and knowledge at one month in the control group with a validated questionnaire (knowledge: check list and true/false questions).
Time frame: 4 weeks
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