The Effectiveness of Core Stability Exercises

NCT03975985 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 87

Last updated 2023-05-09

No results posted yet for this study

Summary

This study assess the effectiveness of core stability exercises performed in subacute phase of stroke. Half of participants will receive conventional physiotherapy, while the other half will receive core stability exercises and core stability exercises plus transcutaneous electrical nerve stimulation (TENS).

Conditions

  • Brain Injury, Vascular
  • Sequelae
  • Stroke Syndrome
  • Movement; Disorder, Treatment-Induced
  • Physical Activity

Interventions

OTHER

Core stability exercises (CSE)

CSE are exercises focused on trunk muscle strengthening, proprioception, selective movements of the trunk and pelvis muscle, and coordination, and will be carried out in supine, sitting on a stable surface and sitting on an unstable surface (physioball). The exercise involves changes in the position of the body without resistance, aiming to improve strength, endurance, proprioception and coordination. \- TENS: Half of the patients assigned to CSE will also receive TENS (highfrequency TENS 100 Hz; 0.2 ms pulse width), administered via TENS stimulator with two disposable 0.9 mm diameter electrodes placed on the skin over the lumbar erector spinae (3 cm lateral to the L3 and L5 spinous process).

OTHER

Conventional Physiotherapy

The common feature of CP is that it consists of a management by the physiotherapist according to the CP may consist in a variety (or combination) of multiple components such as tone normalization, exercises for maintain range of motion, passive mobilization of hemiparetic side, postural control, gait re-education to walking/standing between parallel bars or with a therapist, rehabilitation of the activity of daily living, etc.

Sponsors & Collaborators

  • Universitat Internacional de Catalunya

    collaborator OTHER
  • Parc Taulí Hospital Universitari

    collaborator OTHER
  • Hospital de Terrassa

    collaborator OTHER
  • Hospital de la Santa Creu de Vic

    collaborator UNKNOWN
  • University Ramon Llull

    collaborator OTHER
  • Hospital Sociosanitari Mutuam Girona

    collaborator OTHER
  • Parc de Salut Mar

    collaborator OTHER
  • FIDMAG Germanes Hospitalàries

    collaborator OTHER
  • Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-01-15
Primary Completion
2022-03-15
Completion
2022-03-15

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03975985 on ClinicalTrials.gov