pacemaker implantation. -
Conditions
Interventions
Intervention 1: For Pacemaker patient in experimental group(25), the Cardiac Rehadilitation Program(CR) consisted of a 3 sessions(8 Weeks, every tow weeks,100 min)including exercise training 40 min, e
Rehabilitation
Treatment - Drugs
For Pacemaker patient in experimental group(25), the Cardiac Rehadilitation Program(CR) consisted of a 3 sessions(8 Weeks, every tow weeks,100 min)including exercise training 40 min, education 30 min
For implantable cardioverter defibrillator and synchronized bivantriculare pacing patient in experimental group(25), the Cardiac Rehadilitation Program(CR) consisted of a 3 Sessions(8 Weeks, every tow
For (50) patient in contorl group the routine intervention was done.
Sponsors
Vice chancellore for research, Shiraze university of Midical Scienes
Eligibility
Sex/Gender
All
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: Patients are aged 18-70 years; are of both sex; For the first time device is implanted; Patients who have the ability to participate in the rehabilitation program; speech and hearing problems are not known ; physical mental disability which prevents the ability not participate in session. Exclusion criteria: patient's unwillingness to continue participating in the study
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Adjustment. Timepoint: Befor, 8 Week and 12 Week After Intervention. Method of measurement: Psycho-Social Adjustment Scale(PIAS)).;Bodyimage. Timepoint: Befor,8 Week and 12 Week After Intervention. Method of measurement: Bodyimage And Relationsheep Questionnaire.;Complication. Timepoint: Befor, 8 Week And 12 Week After Intervention. Method of measurement: Researcher Made Questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr.Mahnaz Rakhshan
School of Nursing and Midwifery, Namazi, Square
Outcome results
None listed