THE EFFECT OF PROPRIOCEPTIVE EXERCISE TRAINING ON CERVICAL PROPRIOCEPTION, KINESIOPHOBIA, AND PAIN CATASTROPHIZING LEVELS IN SARCOPENIC GERIATRIC INDIVIDUALS RESIDING IN NURSING HOMES
NCT ID: NCT07253714
Last Updated: 2025-11-28
Study Results
Results pending
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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Recruitment Status
COMPLETED
Clinical Phase
NA
Total Enrollment
31 participants
Study Classification
INTERVENTIONAL
Study Start Date
2024-04-23
Study Completion Date
2024-12-30
Brief Summary
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This study investigated the effects of cervical proprioceptive exercise training on cervical proprioception, kinesiophobia and pain catastrophising in sarcopenic nursing home residents.
In this randomized controlled study, 63 nursing home residents were screened for sarcopenia based on the EWGSOP2 criteria, which include assessments of handgrip strength (Jamar dynamometer), physical performance (4-meter walking test), and muscle mass evaluated by Bioelectrical Impedance Analysis. Thirty-one residents diagnosed with sarcopenia were randomly assigned to either a control group (n = 17), which completed 12 supervised sessions of conventional exercises (postural, cervical range of motion, and isometric exercises) over six weeks, or an experimental group (n = 14), which received an additional 12 sessions of cervical proprioceptive exercises. Both groups were evaluated before and after the intervention. Cervical joint position sense, kinesiophobia, pain catastrophizing, were assessed using the Joint Position Error Test; the Tampa Scale of Kinesiophobia; the Pain Catastrophizing Scale.
In this randomized controlled study, 63 nursing home residents were screened for sarcopenia based on the EWGSOP2 criteria, which include assessments of handgrip strength (Jamar dynamometer), physical performance (4-meter walking test), and muscle mass evaluated by Bioelectrical Impedance Analysis. Thirty-one residents diagnosed with sarcopenia were randomly assigned to either a control group (n = 17), which completed 12 supervised sessions of conventional exercises (postural, cervical range of motion, and isometric exercises) over six weeks, or an experimental group (n = 14), which received an additional 12 sessions of cervical proprioceptive exercises. Both groups were evaluated before and after the intervention. Cervical joint position sense, kinesiophobia, pain catastrophizing, were assessed using the Joint Position Error Test; the Tampa Scale of Kinesiophobia; the Pain Catastrophizing Scale.
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Detailed Description
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Conditions
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Sarcopenia in Elderly
Study Design
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Allocation Method
RANDOMIZED
Intervention Model
PARALLEL
Primary Study Purpose
TREATMENT
Blinding Strategy
NONE
Study Groups
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Experimental group
Cervical proprioceptive exercise and classic exercise were applied.
Group Type
EXPERIMENTAL
Classic exercises
Intervention Type
OTHER
Participants in the control group received classical exercise training for 6 weeks.
Proprioceptive exercise training
Intervention Type
OTHER
Participants in the experimental group received cervical proprioception exercises in addition to classical exercise training for 6 weeks.
Control Group
Classic exercise (Cervical range of motion exercise+posture exercise+isometric exercises) were applied only.
Group Type
ACTIVE_COMPARATOR
Classic exercises
Intervention Type
OTHER
Participants in the control group received classical exercise training for 6 weeks.
Interventions
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Classic exercises
Participants in the control group received classical exercise training for 6 weeks.
Intervention Type
OTHER
Proprioceptive exercise training
Participants in the experimental group received cervical proprioception exercises in addition to classical exercise training for 6 weeks.
Intervention Type
OTHER
Eligibility Criteria
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Inclusion Criteria
* Being 65 years of age or older,
* Being diagnosed with sarcopenia,
* Having at least 91 points or more according to the Barthel daily living activities index (being mildly dependent or completely independent),
* Having 24 points or more according to the mini mental assessment, which is considered mentally healthy.
* Being diagnosed with sarcopenia,
* Having at least 91 points or more according to the Barthel daily living activities index (being mildly dependent or completely independent),
* Having 24 points or more according to the mini mental assessment, which is considered mentally healthy.
Exclusion Criteria
* Having a disability (such as limb, vision, hearing loss),
* Having a serious neurological, orthopedic or rheumatological disorder that may affect proprioception,
* Having uncontrolled hypertension/diabetes,
* Having pain in the spine and/or extremities,
* Having a psychiatric disease diagnosis.
* Having a serious neurological, orthopedic or rheumatological disorder that may affect proprioception,
* Having uncontrolled hypertension/diabetes,
* Having pain in the spine and/or extremities,
* Having a psychiatric disease diagnosis.
Minimum Eligible Age
65 Years
Eligible Sex
ALL
Accepts Healthy Volunteers
No
Sponsors
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Atılım University
OTHER
Sponsor Role
lead
Responsible Party
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Beyza Doğanbaz
pyhsiotherapist
Responsibility Role
PRINCIPAL_INVESTIGATOR
Locations
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Nevia Oran Nursing Home
Ankara, çankaya, Turkey (Türkiye)
Site Status
Countries
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Turkey (Türkiye)
References
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Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
Beyza-ftr-02
Identifier Type: -
Identifier Source: org_study_id
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