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Comparison of Joint Position Sense in Diabetic and Traumatic Transtibial Amputees

Primary Purpose

Diabetic Polyneuropathy, Amputation

Status
Completed
Phase
Not Applicable
Locations
Turkey
Study Type
Interventional
Intervention
Joint Position Sense Analysis
Sponsored by
Recep Tayyip Erdogan University Training and Research Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional screening trial for Diabetic Polyneuropathy focused on measuring Diabetic Polyneuropathy, Lower Extremity Amputation, Joint Position Sense, Compliance With The Prosthesis, Balance, Functional Performance

Eligibility Criteria

45 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Diabetic Group (DG):

  1. Those who had unilateral transtibial amputation due to DPN
  2. Between the ages of 40-65
  3. Completed rehabilitation with prosthesis
  4. Using prosthesis for at least 1 year
  5. With standard size stump length
  6. Without phantom sensation and pain
  7. Able to walk at least 10 m independently
  8. Gross lower extremity muscle strength at least moderate
  9. No cognitive and mental problems
  10. Diabetic nephropathy, retinopathy, ulceration etc. without secondary complications
  11. Those who voluntarily agreed to participate in the research
  12. Not included in any other concurrent study

Traumatic Group (TG):

  1. Those who had trauma-induced unilateral transtibial amputation
  2. Between the ages of 40-65
  3. Completed rehabilitation with prosthesis
  4. Using prosthesis for at least 1 year
  5. With standard size stump length
  6. Without phantom sensation and pain
  7. Able to walk at least 10 m independently
  8. Gross lower extremity muscle strength is at least moderate
  9. Absence of cognitive and mental problems
  10. Those who voluntarily agreed to participate in the research
  11. Not included in any other concurrent study

Exclusion Criteria:

For all groups;

  1. Having osteoarticular deformity in the knee joint
  2. Having an orthopedic or neurological disease other than the cause of amputation
  3. Significant and irreversible visual deficit
  4. Body mass index (BMI)>30 kg/m²
  5. Having a disability that makes it hard to complete any of the tests
  6. Individuals with a history of cancer and receiving chemotherapy

Sites / Locations

  • Hacettepe University

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

Diabetic Group (DG)

Traumatic Group (TG)

Arm Description

Examine the effect of joint position sense on compliance with the prosthesis, balance and functional performance in individuals with lower extremity amputation due to diabetic polyneuropathy.

Examine the effect of joint position sense on compliance with the prosthesis, balance and functional performance in individuals with lower extremity amputation due to traumatic causes.

Outcomes

Primary Outcome Measures

Joint Position Sense
The Xsens DOT Motion Capture System will be used in the evaluation of knee joint proprioception. . Before starting the measurement, the sensors are properly attached to the patient. The sense of proprioception of the knee joint will be evaluated bilaterally with weightless (NWB) using the method. The NWB assessment will be performed with and without prosthesis while the person is in a sitting position with their legs fully supported. The person's eyes will be covered with a band aid to avoid any visual cues. The knee joint in extension position will be slowly brought to the target angle value of 30° and 60° flexion position by the physiotherapist and waited for 4 seconds. After 3 consecutive attempts, the participant will be asked to actively perform the flexion movement whose angle is determined using the same limb. There will be 2 minute rest breaks between measurements. The difference between the target angle and the measured angle is recorded as the margin of error.

Secondary Outcome Measures

The Limits of Stability
The limits of stability were used to evaluate static balance. Limits of stability is the greatest distance in any direction a person can lean away from a midline vertical position without falling, stepping, or reaching for support. Participants were assessed with a force platform (Model BP 5050; Bertec Corporation, Columbus, Ohio) in terms of support surfaces on limits of stability (LoS) in the right, left, front and back directions when the eyes were open on the hard floor with the Bertec Balance System on their preferred support surface width.
Postural Sway
Postural sways were used to evaluate dynamic balance. Postural sway, in terms of human sense of balance, refers to horizontal movement around the center of gravity. Postural sway was measured while quiet standing with open/closed eyes on a hard/soft floor using the Bertec Balance System at their preferred support surface width.
Functional Capacity
2 Minute Walk test was used to evaluate the functional capacity. The test was performed in a corridor on a flat hard surface of 30 m in length in a straight line. Before the examination, the patient rested for 10 min in a sitting position. It is calculated by measuring the distance that the person walks at the end of this period by asking the person to walk for 2 minutes along a 30 m corridor. In cases of chest pain, dyspnea, leg cramps, excessive fatigue, sweating and wilting, the test should be terminated immediately. At one-minute intervals during the test, the participant received information about the time remaining until the end of the test.

Full Information

First Posted
September 13, 2022
Last Updated
June 9, 2023
Sponsor
Recep Tayyip Erdogan University Training and Research Hospital
Collaborators
Hacettepe University
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1. Study Identification

Unique Protocol Identification Number
NCT05542901
Brief Title
Comparison of Joint Position Sense in Diabetic and Traumatic Transtibial Amputees
Official Title
The Comparison of Joint Position Sense in Diabetic and Traumatic Transtibial Amputees and The Investigation of The Relationship Between Compliance With a Prosthesis, Balance, and Functional Performance With Joint Position Sense
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Completed
Study Start Date
September 13, 2022 (Actual)
Primary Completion Date
May 15, 2023 (Actual)
Study Completion Date
June 9, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Recep Tayyip Erdogan University Training and Research Hospital
Collaborators
Hacettepe University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This study evaluated the effect of joint position sense on compliance with the prosthesis, balance and functional performance in individuals with lower extremity amputation due to diabetic polyneuropathy. Study group consisted of 16 subjects with unilateral transtibial amputation due to diabetic polyneuropathy and control group consisted of 16 subjects with unilateral transtibial amputation due to traumatic reasons.
Detailed Description
Proprioception is defined as the ability to distinguish the position of various body parts relative to each other and the ground through the sensory system (kinesthesia) and to perceive the forces acting on these body parts. Proprioception is a function that takes place mainly on a subconscious level. Information about the external environment we live in is obtained from the combination of nerve terminals in muscles and tendons, fibrous capsules around joints, vestibular and visual systems. The proprioceptive information obtained about the external environment through the peripheral nervous system is transferred to the central nervous system. The integration of these data collected from different sensory receptors is performed, and appropriate motor responses are initiated to ensure postural balance. Sensory loss due to pain, fatigue, effusion, trauma, or various neurological, musculoskeletal disorders and metabolic diseases such as diabetes often causes a decrease in proprioceptive sensation in these case groups. Peripheral nerve damage due to diabetic polyneuropathy (DPN), varies depending on the type of nerve fiber affected. As a result of damage to unmyelinated and small myelinated nerve fibers, light touch, pain and temperature senses are impaired while vibration and proprioception senses are decreased as a result of damage to large myelinated nerve fibers. Recent studies have shown that individuals with DPN are more likely to apply to the emergency department due to complications from fall accidents because they experience balance loss during activities of daily living compared to healthy non-diabetic individuals. Furthermore, foot biomechanics, which deteriorates owing to the loss of the normal neural feedback system caused by DPN, causes foot ulcerations by creating aberrant pressure distribution in the foot. In these people, non-healing lower limb ulcers account for 85% of planned lower extremity amputations. Due to the predicted loss of soft tissue, bone, and sensory receptors in the amputated limb following a prior lower extremity amputation, which results in musculoskeletal system degradation and destruction of the mechanoreceptors innervating these tissues, the way these individuals experience their surroundings changes and differentiates them from individuals who have been amputated due to traumatic causes. Diabetic amputees are unable to utilize their prostheses functionally following amputation due to their physical problems, which results in the majority of patients discontinuing usage of prosthesis. Although the number of test batteries developed to assess proprioceptive sense and the effectiveness of rehabilitation protocols used to assess proprioceptive sense in individuals with musculoskeletal disorders such as amputation is insufficient in the literature, it is believed that the existing batteries do not adequately assess proprioceptive sense. Additionally, no study has been conducted to determine the extent to which these patients' proprioceptive sensibility is altered following lower limb amputation due to DPN. For this reason, the study was planned to examine the effect of joint position sense on compliance with the prosthesis, balance and functional performance in individuals with lower extremity amputation due to DPN.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetic Polyneuropathy, Amputation
Keywords
Diabetic Polyneuropathy, Lower Extremity Amputation, Joint Position Sense, Compliance With The Prosthesis, Balance, Functional Performance

7. Study Design

Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
32 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Diabetic Group (DG)
Arm Type
Other
Arm Description
Examine the effect of joint position sense on compliance with the prosthesis, balance and functional performance in individuals with lower extremity amputation due to diabetic polyneuropathy.
Arm Title
Traumatic Group (TG)
Arm Type
Other
Arm Description
Examine the effect of joint position sense on compliance with the prosthesis, balance and functional performance in individuals with lower extremity amputation due to traumatic causes.
Intervention Type
Diagnostic Test
Intervention Name(s)
Joint Position Sense Analysis
Intervention Description
The Xsens DOT Motion Capture System will be used to analyze joint position sense.
Primary Outcome Measure Information:
Title
Joint Position Sense
Description
The Xsens DOT Motion Capture System will be used in the evaluation of knee joint proprioception. . Before starting the measurement, the sensors are properly attached to the patient. The sense of proprioception of the knee joint will be evaluated bilaterally with weightless (NWB) using the method. The NWB assessment will be performed with and without prosthesis while the person is in a sitting position with their legs fully supported. The person's eyes will be covered with a band aid to avoid any visual cues. The knee joint in extension position will be slowly brought to the target angle value of 30° and 60° flexion position by the physiotherapist and waited for 4 seconds. After 3 consecutive attempts, the participant will be asked to actively perform the flexion movement whose angle is determined using the same limb. There will be 2 minute rest breaks between measurements. The difference between the target angle and the measured angle is recorded as the margin of error.
Time Frame
1 week
Secondary Outcome Measure Information:
Title
The Limits of Stability
Description
The limits of stability were used to evaluate static balance. Limits of stability is the greatest distance in any direction a person can lean away from a midline vertical position without falling, stepping, or reaching for support. Participants were assessed with a force platform (Model BP 5050; Bertec Corporation, Columbus, Ohio) in terms of support surfaces on limits of stability (LoS) in the right, left, front and back directions when the eyes were open on the hard floor with the Bertec Balance System on their preferred support surface width.
Time Frame
1 week
Title
Postural Sway
Description
Postural sways were used to evaluate dynamic balance. Postural sway, in terms of human sense of balance, refers to horizontal movement around the center of gravity. Postural sway was measured while quiet standing with open/closed eyes on a hard/soft floor using the Bertec Balance System at their preferred support surface width.
Time Frame
1 week
Title
Functional Capacity
Description
2 Minute Walk test was used to evaluate the functional capacity. The test was performed in a corridor on a flat hard surface of 30 m in length in a straight line. Before the examination, the patient rested for 10 min in a sitting position. It is calculated by measuring the distance that the person walks at the end of this period by asking the person to walk for 2 minutes along a 30 m corridor. In cases of chest pain, dyspnea, leg cramps, excessive fatigue, sweating and wilting, the test should be terminated immediately. At one-minute intervals during the test, the participant received information about the time remaining until the end of the test.
Time Frame
1 week

10. Eligibility

Sex
All
Minimum Age & Unit of Time
45 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diabetic Group (DG): Those who had unilateral transtibial amputation due to DPN Between the ages of 40-65 Completed rehabilitation with prosthesis Using prosthesis for at least 1 year With standard size stump length Without phantom sensation and pain Able to walk at least 10 m independently Gross lower extremity muscle strength at least moderate No cognitive and mental problems Diabetic nephropathy, retinopathy, ulceration etc. without secondary complications Those who voluntarily agreed to participate in the research Not included in any other concurrent study Traumatic Group (TG): Those who had trauma-induced unilateral transtibial amputation Between the ages of 40-65 Completed rehabilitation with prosthesis Using prosthesis for at least 1 year With standard size stump length Without phantom sensation and pain Able to walk at least 10 m independently Gross lower extremity muscle strength is at least moderate Absence of cognitive and mental problems Those who voluntarily agreed to participate in the research Not included in any other concurrent study Exclusion Criteria: For all groups; Having osteoarticular deformity in the knee joint Having an orthopedic or neurological disease other than the cause of amputation Significant and irreversible visual deficit Body mass index (BMI)>30 kg/m² Having a disability that makes it hard to complete any of the tests Individuals with a history of cancer and receiving chemotherapy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Melek M. ERDEM, PT, M.Sc.
Organizational Affiliation
Tayyip Erdogan University Training and Research Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Semra TOPUZ, PT, Prof.
Organizational Affiliation
Hacettepe University
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Ali I. YALCIN, PT, Ph.D.
Organizational Affiliation
Hacettepe University
Official's Role
Study Chair
Facility Information:
Facility Name
Hacettepe University
City
Ankara
State/Province
Altindag
ZIP/Postal Code
06230
Country
Turkey

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
De-identified individual participant data for all primary and secondary outcome measures will be made available.
IPD Sharing Time Frame
Data will be available within 3 months with completion of the result report.
IPD Sharing Access Criteria
Requestors will be required to sign a Data Access Agreement.
IPD Sharing URL
https://orcid.org/0000-0003-4073-3084
Citations:
PubMed Identifier
33909824
Citation
Fontes Filho CHDS, Laett CT, Gavilao UF, Campos JC Jr, Alexandre DJA, Cossich VRA, Sousa EB. Bodyweight distribution between limbs, muscle strength, and proprioception in traumatic transtibial amputees: a cross-sectional study. Clinics (Sao Paulo). 2021 Apr 26;76:e2486. doi: 10.6061/clinics/2021/e2486. eCollection 2021.
Results Reference
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Comparison of Joint Position Sense in Diabetic and Traumatic Transtibial Amputees

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