Pacemaker type may influence arm strength and balance, study finds
NCT ID NCT06775691
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at 60 people with different types of pacemakers to see how the device affects their arm function, balance, physical activity, fear of movement, and quality of life. Researchers measured things like hand strength, walking speed, and daily living tasks. The goal was to understand why some patients don't feel as well as expected after getting a pacemaker.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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60 people
The number who actually took part.
- Started
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Apr 2024
- Finished
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Jan 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients who regularly visit for pacemaker check-ups will be invited to participate in the study.
- Ages
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18 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * At least 3 months have passed since pacemaker implantation and there are no complications in the last pacemaker control, * Being in NYHA class I-II-III, * Patients with no coordination problems, * Volunteering to participate in the research Exclusion Criteria: * Patients with a history of shoulder pathologies prior to pacemaker implantation that may restrict movement of the upper limb (conditions such as severe pain around the shoulder, edema or shoulder dislocation that may restrict upper limb movement), * Patients with a history of shoulder surgery (limitation in range of motion), * Patients who have had a cerebrovascular event resulting in mastectomy or arm involvement on the affected side, * Patients with decompensated heart failure, * Patients with a history of ICD inappropriate shock, * Those with acute myocardial infarction, * Patients with malignancy on active treatment, patients with collagen tissue disease receiving systemic steroids, * Chronic kidney disease patients on dialysis with unstable volume load
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Hitit University Corum Erol Olçok Training and Research Hospital
Çorum, Center, 19000, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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