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

Not Applicable
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.
Registration Number
IRCT20200302046662N1
Lead Sponsor
Shiraz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
68
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

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

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
evel 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.
Secondary Outcome Measures
NameTimeMethod
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