Coronary Artery Disease, Percutaneous Coronary Intervention
Conditions
Brief summary
The purpose of this study is to elaborate an educative program that includes telephone follow-up and assess its impact on the perceived health status of patients submitted to percutaneous coronary intervention.
Interventions
BEHAVIORALeducational program+telephone follow up
Patients will participate in the educational program with telephone follow-up, the education program will initiate in preoperative period and will continue for six months.
BEHAVIORALUsual care
Patients will receive orientations about the surgery and the rehabilitation by health professionals, especially in the discharge. And will have return for evaluation scheduled by health professionals.
Sponsors
University of Sao Paulo
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Adult patients (18 years or more) of both sexes * Being submitted to the first coronary artery bypass graft surgery between April 2011 and July 2012 * Having a properly functioning residential phone line
Exclusion criteria
* No cognitive condition to participate (assessed through the Mini-Mental State Examination - MMSE) * Illiterate participants who did not reach the minimum score 13 on the MMSE * Participants with one to seven years of education who did not reach the minimum score 18 on the MMSE * Participants with eight or more years of education who did not reach the minimum of 26 points on the MMSE
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| change from baseline in perceived health status at six months | baseline and six months | The questionnaire Medical Outcomes Survey 36 - Item Short-Form developed by Ware and Sherboune (1992) will be used to collect the data at baseline and at six months. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| change from baseline in treatment adherence at six months | baseline and six months | The questionnaire Medida de adesão ao tratamento (MAT) developed by Delgado and Lima (2001) will be used to collect the data related to the pharmacological adherence at baseline and at six months. |
| change from baseline in self-efficacy at six months | baseline and six months | The questionnaire General Self-Efficacy Scale developed by Schwarzer and Jerusalem (1995) will be used to collect the data at baseline and at six months. |
| change from baseline in anxiety and depression at six months | baseline and six months | The questionnaire Hospital Anxiety and Depression Scale (HADS) developed by Zigmond and Snaith (1983) will be used to collect the data at baseline and at six months. |
Countries
Brazil
Outcome results
None listed