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Investigation of the effect of cardiac rehabilitation on patients with different types of heart rhythm management devices and their spouses

Investigation of the effect of cardiac rehabilitation via telenursing on sexual satisfaction and fatigue of patients with different types of heart rhythm management devices and their spouses at arrhythmias clinics affiliated to Shiraz University of Medical Sciences

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200302046662N1
Enrollment
68
Registered
2020-03-07
Start date
2020-05-21
Completion date
Unknown
Last updated
2020-03-24

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

Conditions

Condition 1: Patients with different types of heart rhythm management devices. Condition 2: Spouses of patients with different types of heart rhythm management devices.

Interventions

Intervention 1: Intervention group: Intervention group (patient plus his / her spouse) during an 8-week period including 8 sessions of cardiac rehabilitation: 2 in-person sessions including training a

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Has one of a different types of heart rhythm management devices and has been implanted for at least three months Be married Only have one spouse 18 to 70 years old Not diagnosed mental illness and acute cognitive disorders Not having severe orthopedic, neurological, visual and hearing problems Ability to understand and speak and read and write Persian language Phone access (fixed and mobile) after discharge Have sexual activity

Exclusion criteria

Exclusion criteria: Incidence of unstable angina Uncontrolled blood pressure, resting systole greater than 180 mmHg or diastolic resting time greater than 110 mmHg Severe neurological, orthopedic and musculoskeletal problems that occur during the study and prevent them from being active The patient's unwillingness to continue attending the study Not attending one of the pre- or post-test sessions Not attending one of the in person sessions

Design outcomes

Primary

MeasureTime frame
Level of sexual satisfaction in Hudson Index of Sexual Satisfaction questionnaire. Timepoint: At baseline (before intervention) and 2 months after intervention. Method of measurement: Hudson Index of Sexual Satisfaction.;Fatigue score on the Fatigue Severity Scale Questionnaire. Timepoint: At baseline (before intervention) and 2 months after intervention. Method of measurement: Fatigue Severity Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahnaz Rakhshan

Shiraz University of Medical Sciences

rakhshanm@sums.ac.ir0098 7136474254-8

Outcome results

None listed

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