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Effect of stimulation with electrical current associated with exercise in stroke: randomized controlled clinical trial

Effect of interferential current associated with exercise in stroke: randomized controlled clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-22vxvq
Enrollment
Unknown
Registered
2016-10-10
Start date
2015-10-31
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Stroke

Interventions

Initially, patients will be randomly assigned to one of two study groups: active IFC and placebo IFC. In the active IFC group, eighteen patients will undergo interferential current application for fiv
Other
E02.331
E02.779.483

Sponsors

Universidade Federal de Sergipe
Lead Sponsor
Universidade Federal de Sergipe
Collaborator

Eligibility

Age
30 Years to 70 Years

Inclusion criteria

Inclusion criteria: Patients with stroke in mild or moderate spastic phase, both genders, aged 30 to 70 years and without physical therapy concomitant during the training period.

Exclusion criteria

Exclusion criteria: Patients who present score less than 24 on the Mini-mental exam, psychiatric condition, cognitive decline or dementia influencing the communication process, musculoskeletal, neuromuscular, or recent cardiopulmonary disorder, patients who can not walk and sit independently, present anesthesia in the trunk region or refuse to participate.

Design outcomes

Primary

MeasureTime frame
Increase of trunk control of the subjects stimulated by active IFC. For assessment of trunk control, the Trunk Impairment Scale, Postural Assessment Scale for Stroke Patients and Functional Reach Test will be used. And for verification the expected outcome, a variation of at least 5% in scales and test used pre and post intervention will be considered.

Secondary

MeasureTime frame
Reduction of pain intensity at rest and movement, fatigue, catastrophizing and hypertonia, increase of the pressure pain threshold, muscle flexibility and self-esteem. To assess these variables will be used: numerical scale of 11 points, Catastrophizing Pain Scale, modified Ashworth Scale, digital algometry, fleximetry and Rosenberg Self-Esteem Scale, respectively. To check the expected outcomes, a variation of at least 5% in each scale and test used before and after treatment will be considered.

Countries

Brazil

Contacts

Public ContactDaniela Maia

Universidade Federal de Sergipe

danieladacostamaia@gmail.com+557999877677

Outcome results

None listed

Source: REBEC (via WHO ICTRP)