NCT07106619

Brief Summary

Somatosensory dysfunction including the sense of movement and position, i.e. proprioception, is observed in approximately 65% of patients after stroke. Loss of muscle strength, especially in the lower extremities, and impaired proprioception lead to significant loss of function in stroke patients. In addition, recent studies have emphasised that sensory information obtained by target-oriented exercises plays an important role in neuroplasticity and proprioception is an important element. The aim of this study was to evaluate the effect of knee isokinetic muscle strengthening exercises on proprioception and balance in stroke patients.

Trial Health

57
Monitor

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
34

participants targeted

Target at P25-P50 for not_applicable stroke

Timeline
Completed

Started Aug 2025

Shorter than P25 for not_applicable stroke

Geographic Reach
1 country

1 active site

Status
recruiting

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 23, 2025

Completed
9 days until next milestone

Study Start

First participant enrolled

August 1, 2025

Completed
5 days until next milestone

First Posted

Study publicly available on registry

August 6, 2025

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 31, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 31, 2026

Completed
Last Updated

February 24, 2026

Status Verified

July 1, 2025

Enrollment Period

8 months

First QC Date

July 23, 2025

Last Update Submit

February 22, 2026

Conditions

Keywords

stroke rehabilitationproprioceptionisokinetic exercise

Outcome Measures

Primary Outcomes (1)

  • Proprioception assessment with isokinetic test device

    before treatment and at the 3rd week of treatment

Secondary Outcomes (2)

  • Berg scale

    Before treatment and at 3rd week of treatment

  • Time up and Go Test

    Before treatment and at the 3rd week of treatment

Study Arms (2)

Conventional Rehabilitation

ACTIVE COMPARATOR

Patients will receive 15 sessions of conventional rehabilitation

Other: Conventional rehabilitation program

isokinetic Exercise

EXPERIMENTAL

Patients will receive 15 sessions of conventional rehabilitation and 10 sessions of knee isokinetic strengthening exercise therapy for the paretic lower extremity for 3 weeks. Isokinetic strengthening exercises will be performed using Cybex 770, Humac Norm dynamometer (CSMI, Stoughton, MA, USA).

Device: Isokinetic ExercisesOther: Conventional rehabilitation program

Interventions

Ambulation and balance exercises

Conventional Rehabilitationisokinetic Exercise

Exercises will be performed at three different angular speeds (90 ̊/sec, 5 repetitions, 5 sets; 120 ̊/sec, 8 repetitions, 5 sets; 150 ̊/sec, 10 repetitions, 5 sets).

isokinetic Exercise

Eligibility Criteria

Age35 Years - 75 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • At least 3 months and no more than 1 year must have passed since the date of the incident
  • Be between 35 and 75 years of age
  • Manual muscle testing of the affected lower extremity shows at least 3 in ankle dorsiflexion and knee extension
  • No limitation in passive joint range of motion in the lower extremity
  • Mini mental test score \> 23

You may not qualify if:

  • Presence of spasticity according to the modified Ashworth scale \> 1+
  • Presence of neurological disease other than stroke
  • Presence of other medical conditions that may cause sensorimotor dysfunction in the lower extremities (e.g., diabetic polyneuropathy)
  • Presence of orthopaedic problems affecting lower extremity function
  • Previous history of stroke or ischaemic attack
  • Poor general health status (e.g. severe heart failure, COPD)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ankara Etlik City Hospital

Ankara, Yenimahalle, Turkey (Türkiye)

RECRUITING

MeSH Terms

Conditions

Stroke

Condition Hierarchy (Ancestors)

Cerebrovascular DisordersBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesVascular DiseasesCardiovascular Diseases

Central Study Contacts

Ayşe Naz Kalem Özgen, specialist

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER GOV
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
specialist

Study Record Dates

First Submitted

July 23, 2025

First Posted

August 6, 2025

Study Start

August 1, 2025

Primary Completion

March 31, 2026

Study Completion

March 31, 2026

Last Updated

February 24, 2026

Record last verified: 2025-07

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