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The effect of performing self management program on quality of life, anxiety and depression of post coronary angioplasty patients

The effect of performing self management angina plan on quality of life, anxiety and depression of post coronary angioplasty patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT138902162621N7
Enrollment
40
Registered
2011-05-29
Start date
2009-10-11
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Artery Disease. Presence of cardiac and vascular implant and graft, unspecified

Interventions

Intervention 1: An angina self management plan for intervention group took 12 weeks and follow up programm in that time was done by telephone at 1,4,8,12 weeks. Intervention 2: control groups took rou
Behavior
An angina self management plan for intervention group took 12 weeks and follow up programm in that time was done by telephone at 1,4,8,12 weeks.
control groups took routine educations.

Sponsors

Vice chancellor for research, Shirasz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients under angioplasty or coronary vascular stent, age below 70 years, having education at least equal to primary fifth class, the ability of comprehending the educational subjects based on the researcher’s judgment, having the ability of understanding Persian language, inclining to participate in the research, accessibility to telephone to follow up the training plan by researcher. Exclusion criteria: dementia, mental and psychological confusion (according to diagnosis by physician and file records), suffering from severe and life threatening diseases along with coronary vascular disease (according to diagnosis by physician and patient’s file), having anxiety and depression at higher than 11 based on the hospital anxiety and depression scale, participating in compiled formal and informal classes of coronary vascular disease previously (based on patient’s expression), history of coronary artery bypass graft and signing the written informed consent form.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Quality of life. Timepoint: before and 3 months after intervention. Method of measurement: seattle angina questionaire.;Anxiety and Depression. Timepoint: pre test and post test (3 months after intervention). Method of measurement: Hospital Anxiety and Depression Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Marzieh Moattari

Department of Nursing, College of Nursing and Midwifery, Shiraz University of Medical Sciences

moattarm@sums.ac.ir+98 71164742545

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026