Heart Failure Clinical Trials

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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

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patients aged 18 and over with heart failure who are receiving Implantable Cardioverter Defibrillator (ICD) or Cardiac Resynchronization Therapy (CRT)

• At least 3 months have passed since device implantation and there have been no complications at the last device control

• Being in New York Heart Association (NYHA) Class II-III

• Patients without cooperation problems

• Patients who volunteer to participate in the study

Locations
Other Locations
Turkey
Hitit University Erol Olcok Training and Research Hospital, Cardiac Rehabilitation Unit
RECRUITING
Çorum
Time Frame
Start Date: 2026-05-11
Estimated Completion Date: 2027-05-11
Participants
Target number of participants: 36
Treatments
Experimental: High-Intensity Interval Group
Experimental: Moderate Intensity Continuous Group
Active_comparator: Control Group
Related Therapeutic Areas
Sponsors
Leads: Erol Olcok Corum Training and Research Hospital

This content was sourced from clinicaltrials.gov