Clinical trials

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Condition / disease
Location
Status: Not yet recruiting

Comparison of the Effects of Different Upper Extremity Aerobic Exercise Training Protocols on Arm Functional Capacity in Patients With Heart Failure With Cardiac Implantable Electronic Devices

1. To determine the most suitable exercise protocol for upper extremity aerobic exercise training, a widely used type of aerobic exercise to improve reduced upper extremity functional capacity in individuals with CIED and HF. 2. To investigate whether high-intensity intermittent upper extremity aerobic exercise training provides a more effective improvement in upper extremity functional capacity compared to moderate-intensity continuous upper extremity aerobic exercise training. 3. To determine the effectiveness of different types of upper extremity aerobic exercise training compared to lower extremity aerobic training alone in individuals with CIED and HF.

Participants needed: 36
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Erol Olcok Corum Training and Research HospitalUpdated: May 18, 2026
Eligibility criteria

Patients aged 18 and over with heart failure who are receiving Implantable Cardi... [+4]

Patients who have previously participated in a cardiac rehabilitation program an... [+11]

Status: Recruiting

Seasonal Physical Activity in Patients With Heart Failure With Cardiac Implantable Electronic Devices

The aim of this observational study is to determine the effect of seasonal changes on physical activity levels in heart failure patients with cardiac implantable electronic devices. Patients with heart failure who have a cardiac implantable electronic device will be evaluated throughout the year.

Participants needed: 24
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Erol Olcok Corum Training and Research HospitalUpdated: May 8, 2026Locations: 1Duration: 12 Months
Eligibility criteria

Over 18 years of age, [+3]

Being a New York Heart Association (NYHA) Class IV resident [+6]

Status: Recruiting

Assessment of Validity and Reliability of the Turkish Version of the Quality of Life and Related Events Assessment Scale for Pacemaker Patients

Cardiac implantable electronic devices are widely utilized to lower the rates of morbidity and mortality from ventricular tachycardia and ventricular fibrillation, as well as the incidence of sudden cardiac death. Although implantation of these devices increases survival rates, patients may experience acute and chronic complications. These complications include device dislocation and fracture, inappropriate shocks, pocket hematoma, or infection. Furthermore, functional loss in the upper extremity may result from upper extremity restrictions that are applied for an excessively long time in order to ensure proper placement of the device following implantation, or from patients who choose to extend this period on their own initiative out of worry about device failure or dislocation. Patients' quality of life may be negatively impacted by these issues as well as diminished exercise capacity, weariness, and weaker respiratory and peripheral muscles. A quality of life scale called 'The Assessment of Quality of Life and Related Events (AQUAREL)' was developed by Stoffmel et al. for patients using pacemakers. In this study, the validity and reliability study of the Turkish version of the AQAREL Scale will be conducted.

Participants needed: 120
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Erol Olcok Corum Training and Research HospitalUpdated: May 8, 2026Locations: 1
Eligibility criteria

Having a pacemaker implant and not having any complications at the last pacemake... [+3]

• Patients with insufficient dementia or cognitive impairment due to multiple co... [+2]