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The effect of cardiac rehabilitation on anxiety, depression and stress in elders with Coronary Artery Disease

Effect of phase I cardiac rehabilitation program on the rate of anxiety, depression and stress in elder coronary patient

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016022726794N1
Enrollment
70
Registered
2017-01-12
Start date
2016-06-21
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

Depression,Anxiety,Stress. Mild depressive episode,Moderate depressive episode,Other depressive episodes,Specific (isolated) phobias,Other phobic anxiety disorders,Panic disorder [episodic paroxysmal anxiety],Mixed anxiety and depressive disorder,Acute stress reaction,Post-traumati

Interventions

Intervention 1: Intervention 1: the experimental group in addition to receiving usual care, will participate in phase 1cardiac rehabilitation program. Phase 1 cardiac rehabilitation program included
Rehabilitation
Treatment - Drugs
Intervention 1: the experimental group in addition to receiving usual care, will participate in phase 1cardiac rehabilitation program. Phase 1 cardiac rehabilitation program included self care and s
Intervention 2 : There will be no intervention for control group . Current treatment

Sponsors

Shahid Sadoughi University of Medical Sciences and Health Services
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 100 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: aged =60 years, ability to understand and speak Persian, coronary artery disease is confirmed by cardiologist. Exclusion criteria: presence of mental and psychologic diseases, Physical limitation or orthopedic including rheumatologic diseases, A history of confusion and forgetfulness, dementia, medications for mental disorders.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Depression. Timepoint: pre intervention- 2month post intervention. Method of measurement: DASS-21 Questionnaire.;Anxiety. Timepoint: pre intervention- 2month post intervention. Method of measurement: DASS-21 Questionnaire.;Stress. Timepoint: pre intervention- 2month post intervention. Method of measurement: DASS-21 Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactTeimouri Javad

Shahid Sadoughi University of Medical Sciences Yazd, School of Nursing & Midwifery

javad-teimouri@ssu.ac.ir javadteimouri1369@yahoo.com+98 35 3824 1751

Outcome results

None listed

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