Comparative study of the effect of the intervention of real Transcranial Led Therapy and placebo, on anxiety and depression with patients with TBI.
Not Applicable
Recruiting
- Conditions
- Craniocerebral Trauma, anxiety, depression, Pathological conditions, signs and symptoms, Low-Level Light TherapyC10.900.300F01.470.132F01.145.126.350E02.594.540
- Registration Number
- RBR-8jcwjp
- Lead Sponsor
- Centro Universitário UniFacid
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- Not specified
Inclusion Criteria
subject between 18 and 60 years old; ability to understand and follow instructions in Portuguese; Glasgow Coma Scale of entry equal to or greater than 12; TBI time from 3 months.
Exclusion Criteria
subjects under 18 or over 60; limiting language and / or motor impairment; non-signature of the informed consent form, presence of important bone defects in the regions of the skull to be stimulated, presence of epilepsy after uncontrolled TBI.
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Reduction in the level of anxiety measured through Beck Anxiety inventories.Each participant will have three assessments, one before treatment, one immediately after treatment and another three months after the end of the intervention.;Reduction in the level of depression measured through the Beck Depression inventories.Each participant will have three assessments, one before treatment, one immediately after treatment and another three months after the end of the intervention.
- Secondary Outcome Measures
Name Time Method Secondary outcomes are not expected