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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02498730
Other study ID # UFRJ-01
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 2015
Est. completion date July 2017

Study information

Verified date July 2022
Source Universidade Federal do Rio de Janeiro
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Our main objective will be to evaluate the chronic effects (12 weeks) of high-intensity interval training compared to moderate intensity (same total work) on reducing the symptoms of bipolar disorder, cortical changes, as well as on the VO2max. In addition, the investigators will establish what influence of gain to VO2max has on reducing symptoms.


Description:

Physical exercise has significant effects on health promotion and the consequent reduction of the severity of bipolar disorder (BD). This review establishes a pattern of response of exercise and potential impact on the pathophysiology of BD; , as well as, produces hypotheses on how acute and chronic effect of exercises may act differently; and provides future perspectives with the focus of the exercise as an important and innovative model of treatment for BD and mental disorder. A critical evaluation of the literature was undertaken including the influence of exercise on health promotion in patients with mental disorders, neurochemical behavior exercise-induced, as well as reflective introduction of news perspectives of training control in severe exercise domain. The exercise induces significant changes in monoaminergic after, and with long-term training, and work with a threshold of exercise can modulate positive effects on mood. Fast adaptive effects from the high intensity interval training should be considered in BD patients. However, there must be caution in his administration. We speculate that exercise may be a way of maintaining euthymia in the case of BD, making it less vulnerable patient to stay longer at a time of neutrality. Future research is needed to adopt a training strategy that is both time efficient in the different areas and adequate for the population in question.


Recruitment information / eligibility

Status Completed
Enrollment 36
Est. completion date July 2017
Est. primary completion date July 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 59 Years
Eligibility Inclusion Criteria: - Bipolar Criteria (DSM-IV), - sedentary lifestyle Exclusion Criteria: - 60 and over, - Cardiovascular Disease, - Panic disorder, - Metabolic syndrome Diagnosis

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Interval Training
High Intensity Interval Training at 100% VO2Max
Continuous Training
Continuous Stimulous at 60% VO2Max
Control
Only Dependent Variables Measures

Locations

Country Name City State
Brazil Institute of Psychiatry (IPUB) Rio de Janeiro

Sponsors (1)

Lead Sponsor Collaborator
Universidade Federal do Rio de Janeiro

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary Symptom Scales (Hamilton and Young) Variable Measured to reduction of symptoms 0 week, 6 week, 12 week
Secondary Cortical Changes (EEG) - Loreta Measured to evaluate changes due to training 0 week, 6 week, 12 week
Secondary VO2Max Variable Measured to assess cardiovascular improvement 0 week, 6 week, 12 week
Secondary Cognitive Function Executive Function, Time Reaction, Atention, and Memory 0 week, 6 week, 12 week
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