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The Effect of Sexual Rehabilitation program on Anxiety, Stress,Depression and Sexual Function in Heart Patients

The Effect of Sexual Rehabilitation Program on Anxiety, Stress, Depression and Sexual Function in Men With Coronary Artery Disease

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016111224919N6
Enrollment
80
Registered
2017-07-12
Start date
2017-04-19
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. Atherosclerotic heart disease

Interventions

Intervention 1: The Observation Group Patients Receive Only the Routine Cares. Intervention 2: The Patients of Test Group Receive Face to Face Instruction, Educational Pamphlets and 20 minutes Sound C
Rehabilitation
The Observation Group Patients Receive Only the Routine Cares.
The Patients of Test Group Receive Face to Face Instruction, Educational Pamphlets and 20 minutes Sound CD s Includes Pelvic Extensore Muscle Exercise Training When Discharged from Hospital.

Sponsors

Kerman University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Married Patients; Age of 18-65; not Suffering from Psychological Disorders, and Diseases Affecting Function such as Urinary System; Nervous System and Skeletal Diseases; Men having Literacy Skill; Filling the Form of Agreement for Participating in The Study Exclusion criteria: Leaving the Study Process and Disinclination to Cooperation; Occuring any Unpleasant Events During The Research

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Stress. Timepoint: Before The Intervention, One Month After The Iintervention. Method of measurement: Questionnaire Dass21.;Anxiety. Timepoint: Before The Intervention, One Month After The Intervention. Method of measurement: dass 21.;Depression. Timepoint: Before TheIintervention, One Month After The Intervention. Method of measurement: dass 21.;Sexual Function. Timepoint: Before The Intervention, One Month AfterThe Intervention. Method of measurement: International Erectile Function Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh.Rafati

Kerman University of Medical Sciences? Pardis oloompezeshki, Haft bagHe

Fatemeh.rafati3179@gmail.com+98 34 3132 5000

Outcome results

None listed

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