NCT05973279

Brief Summary

Stroke is defined as a neurological disorder attributed to acute focal damage of the central nervous system from a vascular cause, including cerebral infarction, intracerebral haemorrhage and subarachnoid haemorrhage. The World Health Organisation defines stroke as a focal and sometimes global impairment of cerebral function that lasts longer than 24 hours or ends in death, develops rapidly, has no demonstrable cause other than a vascular cause. Evaluation of muscle strength and balance ability of affected patients is critical for the recovery of lower extremity motor functions. Proprioception encompasses various sensory perception modalities such as force, effort, movement and limb position. Impairment of sensory function in patients with haemiplegia can hinder the ability of muscles to recover during walking. Accurate and effective assessment of gait and balance functions and their subsequent improvement is one of the primary goals of stroke rehabilitation programmes. Studies comparing the effects of lower extremity functionality and knee joint position sense on balance and falls are available in various versions in the literature. However, there is no study in which 'Restorative Therapies RT300 leg/arm/cor' device was used to measure functionality, 'Humac Norm Isokinetic Machine' was used to measure knee joint position sense, and 'Tecno Body Prokin Isokinetic Balance System' was used to measure balance in a single simultaneous study. Therefore, the aim of this study was to investigate the relationship between lower limb functionality and knee joint position sense with balance and fall parameters in patients with hemiplegia using various devices.

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
60

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Sep 2023

Shorter than P25 for all trials

Status
unknown

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

July 26, 2023

Completed
7 days until next milestone

First Posted

Study publicly available on registry

August 2, 2023

Completed
1 month until next milestone

Study Start

First participant enrolled

September 1, 2023

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2023

Completed
8 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2024

Completed
Last Updated

September 7, 2023

Status Verified

September 1, 2023

Enrollment Period

1 month

First QC Date

July 26, 2023

Last Update Submit

September 6, 2023

Conditions

Keywords

ProprioceptionJoint Position SenseHemiplegiaLower Limb FunctionalityBalanceFall

Outcome Measures

Primary Outcomes (4)

  • Balance and knee joint position

    Knee joint position sense is related to balance in haemiplegic patients.

    First day

  • Lower extremity functionality and balance

    In haemiplegic patients, the level of lower extremity functionality is related to balance.

    First day

  • Falling and knee joint position

    Knee joint position sense is associated with falls in haemiplegic patients.

    First day

  • Lower extremity functionality and falling

    Lower extremity functionality is associated with falls in haemiplegic patients.

    First day

Study Arms (1)

Hemiplegic patients

Other: Tecno Body Prokin Isokinetic Balance SystemOther: Restorative Therapies RT300 leg/arm/cor:Other: CSMI (CYBEX) Humac Norm Isokinetic Test and Exercise System

Interventions

It provides objectively measurable data in static and dynamic balance measurements. The moving balance platform of the system, which is driven by air piston servo motors, can measure at a working angle of 15 degrees in all directions. The results can be monitored and recorded live on the screen on the device. From these data, each individual's static and dynamic balance score is obtained by summing the forward-backward standard deviation and right-left standard deviation.

Hemiplegic patients

RT300 is a motorised treatment system. In general there are 3 systems; Passive therapy, Active therapy and a combination of active therapy with some assistance from the motor. The device can be used from a chair, wheelchair or bed and there are two variants that can be used separately; Leg system, Arm system. Electrodes placed on the skin over specific muscle groups are connected via a cable or wirelessly to the RT300. These are used to stimulate peripheral motor nerves, causing the muscles to work. The software of the SAGE controller unit of the RT300 monitors the treatment process, including the stimulation patterns sent to the arms or legs, and the operation of the ergometer motor to produce smooth cycling motion. Contraindicated in the presence of lower limb fractures or pregnancy.

Hemiplegic patients

22 isolated joint movement models, 4 resistance modes (isokinetic, isotonic, isometric and passive) and a large number of reports to meet the measurement and exercise needs of today's clinicians and researchers. The exercise modes of the device include; Continuous passive movement, multi-angle isometry, proprioception training, standard and eccentric focused isokinetic strengthening, deceleration training, dynamic isotonic training, strength training. Test modes of the device include; Proprioceptive, co-measured, standard isokinetic, concentric/eccentric isokinetic, intermittent stroke isokinetic test.

Hemiplegic patients

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Hemiplegic patients

You may qualify if:

  • Individuals over 18 years of age
  • Volunteering to participate in the study

You may not qualify if:

  • Hip and knee prosthesis
  • Being diagnosed with vertigo
  • Having a history of serious neurological diseases such as Parkinson's disease, multiple sclerosis except hemiplegia
  • Having a previous operation for the lower limb
  • Poor co-operation

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Hemiplegia

Condition Hierarchy (Ancestors)

ParalysisNeurologic ManifestationsNervous System DiseasesSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Adnan Demirel

    Izzet Baysal Physiotherapy and Rehabilitation Training and Research Hospital

    STUDY DIRECTOR

Central Study Contacts

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
OTHER
Target Duration
1 Year
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
INVESTIGATOR

Study Record Dates

First Submitted

July 26, 2023

First Posted

August 2, 2023

Study Start

September 1, 2023

Primary Completion

October 1, 2023

Study Completion

June 1, 2024

Last Updated

September 7, 2023

Record last verified: 2023-09