Effects of Sarcopenia on Proprioception, Kinesiophobia, and Pressure Pain Threshold
The Effects of Sarcopenia on Cervical Proprioception, Kinesiophobia and Pressure Pain Threshold in Geriatric Nursing Home Residents
1 other identifier
observational
31
1 country
1
Brief Summary
The aim of this observational study is to reveal the effect of sarcopenia on cervical proprioception, kinesiophobia and pressure pain threshold in geriatric individuals living in a nursing home. The main questions it aims to answer are as follows: The presence of sarcopenia in geriatric individuals living in a nursing home is effective/not effective on cervical proprioception. The presence of sarcopenia in geriatric individuals living in a nursing home is effective/not effective on kinesiophobia. The presence of sarcopenia in geriatric individuals living in a nursing home is effective/not effective on pressure pain threshold. As a result of the evaluations, we will obtain the answers to the above questions with the surveys and measurements conducted with the participants divided into two groups as control and sarcopenia groups.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Apr 2025
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 14, 2024
CompletedStudy Start
First participant enrolled
April 1, 2025
CompletedFirst Posted
Study publicly available on registry
December 8, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
January 30, 2026
CompletedDecember 15, 2025
March 1, 2025
9 months
November 14, 2024
December 7, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Assessment of cervical proprioception
Cervical proprioception was assessed using joint position error test . While seated, the participant faced a board positioned 90 cm away at head level, consisting of concentric circles (40 cm diameter, 1-cm increments), and wore a cap with a mounted laser pointer The participant first aligned the laser with the central point to establish the neutral position, then-with eyes open-was guided through flexion, extension, right/left rotation, and right/left lateral flexion, returning to neutral after each movement. The same six movements were then actively performed with eyes closed . Six repetitions were completed for each direction, and the point at which the laser stopped was marked on the board after every trial . The mean of these points was calculated, and angular deviation from the target was determined using the arctan method based on the fixed distance to the board. A deviation of more than 4 degrees was considered to indicate impaired proprioception.
0-8 months
Assessment of kinesiophobia
Kinesiophobia was assessed using the Kinesiophobia Causes Scale (KCS) . Developed by Kocjan and Knapik, the scale identifies the biological and psychological sources of fear of movement and contributes to understanding the underlying causes of reduced motor activity. It comprises two domains: biological and psychological. The biological domain includes morphological factors, movement requirements, energy resources, biological drives, negative experiences, motor competence, and beliefs related to body care, while the psychological domain assesses factors such as confidence, self-efficacy, and social interaction that contribute to avoidance behavior . The Turkish validity and reliability study was conducted by Çayır et al. The greater this value in the range of 0-5, the more valid the person's level of kinesiophobia.
0-8 months
Assessment of pressure pain threshold
A pressure algometer (Baseline Force Gauge Model 12-0304; Baseline, NY, USA) will be used to assess the pressure pain threshold. The patient will be seated, and pressure will be applied perpendicularly and bilaterally using the algometer to different points in the cervical region (2 cm lateral to the C2 and C7spinous processes, at the midpoint of the upper part of the trapezius muscle) at a rate of approximately 3 N/s over an area of 0.5 cm² . The participant will be asked to report the moment they first felt discomfort and the pressure value at this moment will be recorded as the "pressure pain threshold". A second measurement will be taken at each region after an interval, the average of the two measurements will be noted.
0-8months
Study Arms (2)
control group
individuals without sarcopenia
sarcopenic group
individuals with sarcopenia
Eligibility Criteria
Geriatric people who lives in a nursing home in Ankara called Nevia Oran nursing home
You may qualify if:
- Being 65 years of age or older
- Receiving a score of 24 or higher, which is considered mentally healthy, according to the mini mental assessment
- Having at least 91 points or more according to the Barthel daily living activities index (being mildly dependent or completely independent)
You may not qualify if:
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Nevia Oran Nursing Home
Ankara, çankaya, 06530, Turkey (Türkiye)
Related Publications (45)
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BACKGROUND
Related Links
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
nagihan acet, assistant professor
atılım üniversity
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- CROSS SECTIONAL
- Target Duration
- 2 Months
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- pyhsiotherapist
Study Record Dates
First Submitted
November 14, 2024
First Posted
December 8, 2025
Study Start
April 1, 2025
Primary Completion
December 31, 2025
Study Completion
January 30, 2026
Last Updated
December 15, 2025
Record last verified: 2025-03
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- CSR
only IPD used in the results