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Effects of Modified Constraint-Induced on Chronic Stroke Patients

Comparison of the Effect of Proprioceptive Training Therapy or Modified Constraint-Induced Movement Therapy on Upper Extremity Physical Functions in Chronic Stroke Patients - A Randomized Controlled Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04873908
Enrollment
45
Registered
2021-05-05
Start date
2021-05-05
Completion date
2021-09-20
Last updated
2021-10-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke, Rehabilitation

Keywords

Modified constraint-induced therapy, Proprioceptive Training, conventional rehabilitation

Brief summary

In the present study, it was aimed to compare the proprioception training applied in addition to conventional treatment and Modified Constraint-Induced Movement Therapy treatment in patients with chronic strokes and to investigate the effects on proprioception, spasticity, functional motor skills and daily living activities in the upper extremity.

Interventions

OTHERmodified constraint-induced therapy

Patients received conventional rehabilitation and modified constraint-induced therapy schedule

Patients received conventional rehabilitation and Proprioceptive Training schedule

OTHERconventional rehabilitation

Patients received conventional rehabilitation schedule

Sponsors

Acibadem University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
40 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Post stroke hemiparetic patients of six months * spasticity ≤ Grade -3 on modified Ashworth scale * those patients capable of extension of at least 10º each at Metacarpophalangeal (MCP), Proximal Interphalangeal (PIP) and Distal Interphalangeal (DIP) joints and 20º at wrist joint * a score of 24 or higher on the Modified Mini-Mental State Examination * no excessive pain in the affected upper limb, as measured by a score of 4 or higher on a 10-point visual analog scale

Exclusion criteria

* Patients with history of previous stroke, * angina, * uncontrolled hypertension, on medication that could impair neuromuscular performance, * wrist or finger pathologies, significant visual or hearing impairment, * balance problems which may compromise safety during sound upper limb constraint, * unwilling to participate

Design outcomes

Primary

MeasureTime frameDescription
Fugl-Meyer assessment testScore change after 6 weeks of intervention compared to baselineThe Fugl-Meyer Assessment (FMA) is a stroke-specific, performance-based upper extremity function. The maximum available score is 66 and The minimum available score is zero.The higher total score means better motor function in the arm
Action Research arm testScore change after 6 weeks of intervention compared to baselineThe Action Research Arm Test (ARAT) is a 19 item observational measure used by physical therapists and other health care professionals to assess upper extremity performance. The maximum available score from the 19 items was 57. The higher total score means better motor function in the arm
Motor Activity LogScore change after 6 weeks of intervention compared to baselineDaily use of the affected upper extremity was assessed using Motor Activity Log. It is a self-statement questionnaire to determine the frequency and quality of movement in the upper extremity. Score range is 0-5, The higher total score means better motor function in the arm

Secondary

MeasureTime frameDescription
Modified Ashworth ScaleScore change after 6 weeks of intervention compared to baselineModified Ashworth Scale was measure muscle spasticity. It is among the most commonly used scales for clinical and research purposes. The resistance against passive movement is evaluated on a scale of 0-4 points.The lower total score means better spasticity in the arm
thumb localizing testScore change after 6 weeks of intervention compared to baselineA proprioception examination, called the 'thumb localizing test' (TLT), is described as a technique for testing 'limb localization'. With the patient's eyes closed, the examiner positions one of the patient's upper limbs (fixed limb) and asks him to pinch the thumb of that limb with the opposite thumb and index finger (reaching limb).It is evaluated on a 0-3 point scale. The lower the total score, the better the proprioceptive in the arm.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026