Investigating the effect of pulmonary rehabilitation on sexual satisfaction and sexual self-efficacy of patients with chronic obstructive pulmonary disease

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20130812014333N205

Enrollment

Registered

2023-07-19

Start date

2023-07-15

Completion date

Unknown

Last updated

2023-07-25

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

Conditions

Chronic Obstructive Pulmonary Disease. Chronic obstructive pulmonary disease, unspecified

Interventions

Intervention 1: The intervention group will undergo pulmonary rehabilitation training for 8 weeks (one hour per session). Intervention 2: The control group will not receive any intervention.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Informed consent A definitive diagnosis of COPD by a doctor A physically and sexually healthy wife

Exclusion criteria

Exclusion criteria: History of suffering from sexual problems and diseases Smoking history History of heart disease

Design outcomes

Primary

Measure	Time frame
Sexual satisfaction. Timepoint: The beginning of the study and the end of the study (one month later). Method of measurement: Sexual satisfaction questionnaire.;Sexual self-efficacy. Timepoint: The beginning of the study and the end of the study (one month later). Method of measurement: Sexual self-efficacy questionnaire.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahdi Jalali

Islamic Azad University, Khorasgan branch

mahdi.jalali@yahoo.com+98 31 3535 4001

Outcome results

None listed

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