Chronicity Dependence of a Balance Training in Adults Post-stroke

Overview

The level of stroke chronicity has been proposed as an influential variable related to functional balance. However, little is known about the effect of this variable on the effectiveness and maintenance of gains of physical therapy interventions on balance. The objective of this study is to determine the influence of time since injury on the rehabilitation of balance after stroke. Participants will be assigned to a least (6-12 months), a moderate (12-24 months), or a most chronic (> 24 months) group. All the participants will train for 20 one-hour sessions, administered three to five times a week, combining conventional physical therapy exercises and customized exercises interfaced on a balance board that promotes the training of the ankle and hip strategies. Participants will be assessed before, after the intervention, and one month later with a posturography test (sway speed and limits of stability) and clinical scales (Berg Balance Scale, Functional Reaches Test, 30-Second Sit-to-Stand Test, Timed Up and Down Stairs Test, Stepping Test, Timed Up-and-Go Test, and the 10-meter Walking Test).

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: Randomized
    • Intervention Model: Parallel Assignment
    • Primary Purpose: Treatment
    • Masking: Single (Outcomes Assessor)
  • Study Primary Completion Date: January 2016

Interventions

  • Other: balance virtual rehabilitation

Arms, Groups and Cohorts

  • Experimental: intervention (6-12 months)
    • Participants with a chronicity between 6-12 months
  • Experimental: Intervention (12-24 months)
    • Participants with a chronicity between 12-24 months
  • Experimental: Intervention (>24 months)
    • Participants with a chronicity >24 months

Clinical Trial Outcome Measures

Primary Measures

  • Balance Berg Scale
    • Time Frame: up to 1-month follow-up

Participating in This Clinical Trial

Inclusion Criteria

  • Age ≥ 50 and ≤ 65 years old
  • Chronicity > six months
  • Fairly good cognitive condition defined by scores in the Mini-Mental State Examination above 23
  • Ability to walk 10 meters indoors with or without technical orthopaedic aids.

Exclusion Criteria

  • Impaired comprehension that hinder sufficient understanding of the instructions defined by Mississippi Aphasia Screening Test scores below 45
  • Unilateral spatial neglect
  • Ataxia or any other cerebellar symptom
  • Severe auditory or visual impairments
  • Motional or behavioural circumstances that impede adequate collaboration.

Gender Eligibility: All

Minimum Age: 50 Years

Maximum Age: 65 Years

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • Hospitales Nisa
  • Collaborator
    • Universitat Politècnica de València
  • Provider of Information About this Clinical Study
    • Sponsor

Clinical trials entries are delivered from the US National Institutes of Health and are not reviewed separately by this site. Please see the identifier information above for retrieving further details from the government database.

At TrialBulletin.com, we keep tabs on over 200,000 clinical trials in the US and abroad, using medical data supplied directly by the US National Institutes of Health. Please see the About and Contact page for details.