Preoperative Anxiety
Conditions
Keywords
Coronary Angiography
Brief summary
The main objective of this study is to evaluate the impact on preoperative anxiety of an education and information program conducted prior to non-urgent coronary angiography performed in patients hospitalized at the Nîmes University Hospital.
Detailed description
The secondary objectives of this study are to assess the impact of the HEARTLINK program on the following parameters: A. Duration of hospital stay; B. Per operative blood and heart rate?; C. Patient satisfaction (visual analog scale).
Interventions
OTHERInclusion visit
This visit takes place between days -15 and -7 preceding a coronarography scheduled for Day 0. It is part of standard care and corresponds to a required cardiology consultation.
OTHERNurse consultation
This visit takes place on the same day as the inclusion visit and includes practical advice concerning the hospital stay, explanations concerning the surgical act and practical advice on its implementation, information on the length of stay and after. An explanatory booklet concerning the surgical procedure is provided to the patient.
OTHERTelephone contact
A nurse will telephone the patient 72h to 48h before the coronarography scheduled for day 0. During the telephone conversation the nurse will assess the patient's knowledge about his/her pathology, his/her examination and the course of hospitalization. The nurse will answer any questions and if needed provide further information.
PROCEDURECoronarography on day 0
This coronarography is scheduled as part of the patient's routine care. This is not an experimental intervention under evaluation.
Sponsors
Centre Hospitalier Universitaire de Nīmes
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to 79 Years
Healthy volunteers
No
Inclusion criteria
* The patient must have given his/her informed and signed consent * The patient must be insured or beneficiary of a health insurance plan * Patient for whom elective coronary angiography is indicated * The patient has never had a coronary angiography before
Exclusion criteria
* The patient is participating in another study * The patient is in an exclusion period determined by a previous study * The patient is under judicial protection, under tutorship or curatorship * The patient refuses to sign the consent * It is impossible to correctly inform the patient * The patient is pregnant or breastfeeding * The subject has already had a coronary angiography * The subject has a cognitive impairment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Amsterdam Preoperative Anxiety and Information Scale (APAIS) | Day 0 (within 1 hour preceding a coronography) |
Secondary
| Measure | Time frame |
|---|---|
| Duration of hospitalization | Date hospital discharge (expected maximum of 5 days) |
| Blood pressure | Day 0 (within 1 hour preceding a coronography) |
| Cardiac frequency (beats per minute) | Day 0 (within 1 hour preceding a coronography) |
| Visual analog scale for satisfaction concerning care | Day 0 (within 1 hour preceding a coronography) |
Countries
France
Outcome results
None listed