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Clinical Trials/NCT03991390
NCT03991390
Completed
N/A

Effectiveness of Visual Feedback Laser and Core Stability Exercises for Balance Impairment in Subacute Stroke Patients With Pusher Syndrome

Parc Sanitari Pere Virgili1 site in 1 country16 target enrollmentNovember 20, 2018

Overview

Phase
N/A
Intervention
Not specified
Conditions
Pusher Syndrome
Sponsor
Parc Sanitari Pere Virgili
Enrollment
16
Locations
1
Primary Endpoint
Change of Contraversive Pushing at 30 days
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

The objective of this study is to evaluate whether the application of two laser visual feedback exercises and core stability exercises can positively influence postural orientation and the perception of postural verticalization compared to conventional treatments, with the final goal of improving the balance in sitting and standing and the functionality in activities of daily living.

Detailed Description

Study designed as a randomized clinical trial. The total sample (N=16) will randomized into two groups: treatment vs. control. All of them suffering from subacute stroke and pusher syndrome. The study intervention will last 4 weeks. The control group will receive usual rehabilitation treatment for patients with stroke and pusher syndrome (60 minutes per day/5 days per week). The intervention group will receive usual rehabilitation treatment for patients with stroke and pusher syndrome (30 minutes per day/5 days per week) plus 30 minutes of therapy based on the specific protocol designed for the study. This protocol will consist of Core Stability exercises and visual feedback with lasers, both procedures will be alternated one day each. The evaluation of the intervention program will be based on the established objectives, assessing: 1) Pushing Intensity (controversial push scale (SCP)), 2) Laterality (Burke Scale (BLS)), 3) Balance (Postural Assessment Scale for Stroke Patients (S-PASS)), 4) patient functional capacity (Barthel Index), and 5) Quality of Life (Newcastle Stroke-Specific Quality of Life Measure (NEWSQOL)). These variables will be evaluated baseline and post-intervention. Additionally, SCP, BLS and S-PASS will be assessed 15 days after starting treatment.

Registry
clinicaltrials.gov
Start Date
November 20, 2018
End Date
June 30, 2020
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Parc Sanitari Pere Virgili
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients ≥18 years admitted to an intermediate care unit after suffering from subacute stroke, for functional recovery.
  • Diagnosis of ischemic or hemorrhagic stroke confirmed by Magnetic Resonance Imaging (MRI) or Computed Tomography (CT) scan.
  • Pusher syndrome identified by the Scale for Contraversive Pushing (SCP) with a score of ≥2 and by Burke Lateropulsion Scale (BLS) with a value of ≥3.

Exclusion Criteria

  • Patients with severe previous functional dependence (Barthel Index ≤60)
  • Patients diagnosed with dementia GDS-4 or previous severe cognitive impairment.
  • Patients diagnosed with delirium.
  • Patients diagnosed with Wernicke's aphasia.
  • Patients with a previous severe visual deficit that prevents them from continuing activity (retinopathy, cataracts, etc.)
  • Patient with a history of other causes of balance impairment.
  • Patients with orthopedic conditions that difficult the performance of the proposed rehabilitation treatment.
  • Patients enrolled in other research studies.

Outcomes

Primary Outcomes

Change of Contraversive Pushing at 30 days

Time Frame: Baseline (admission), 15 days, 30 days

The Scale for Contraversive Pushing (SCP) allows to diagnose and quantify the pushing behavior of the post-stroke patient. This scale is based on the three main signs of pusher behavior: * Symmetry of the spontaneous posture, * Push of the upper or lower non-affected limb towards the affected side, * Resistance to a passive correction of posture, Assigning up to 1 point in each subscale and in each position. The maximum score is 6, this being the maximum expression of the pusher behavior.

Change of Lateropulsion at 30 days

Time Frame: Baseline (admission), 15 days, 30 days

The Burke Lateropulsion Scale (BLS) is a complementary scale appropriate to the "Contraversive Pushing" scale in the follow-up of patients with pusher behavior in relation to the resistance to passive correction shown by the patient in supine, turning, sitting, standing, walking and transfers scoring up to 17 points. The scale evaluates the patient in sitting and standing position. The patient will be tilted 30º to the affected side and will be asked to return to the vertical position, according to the degrees where resistance appears will be given a score (0 there is no resistance, 1 resistance that begins at 5º, 2 the resistance begins at 10º, 3 the resistance begins above 10º) and the examiner will score if it is (0-null,1-light, 2-moderate, 3-severe) and the same will be evaluated when standing. Interobserver reliability has been shown to be effective for therapy.

Change of Balance at 30 days

Time Frame: Baseline (admission), 30 days

The S-PASS scale has been validated for post-stroke patients in Spanish. It consists of 12 items and is subdivided into two: mobility (7 items) and balance (5 items). The total score of the scale is 36 points and the score goes from 0 to 3 on each item. The scale also quantifies the help the patient needs to perform each action. In items 1 to 4 and 8, control of the trunk is evaluated, both on the affected side and on the non-affected side. Items 5 to 7 report anticipatory postural adjustments, in transfers. Items 9 and 10 assess the balance in standing with and without help, respectively, and finally, on items 11 and 12, the one-leg support in affected and not affected leg without help.

Secondary Outcomes

  • Change of Quality of Life at 30 days(Baseline (admission), 30 days)
  • Change of Independence in the basic activities of daily life at 30 days(Baseline (admission), 30 days)

Study Sites (1)

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