Detraining in People Living With HIV/AIDS

Universidade Federal do Rio Grande do Norte2 enrolled

Overview

The goal of this study was to evaluate the effect of detraining in the components of physical aptitude of people living with HIV/Aids (PVHA).

The study was experimental with a sample composed by an Experimental Group (EG) with 11 PVHA, under antiretroviral therapy and a Control Group (CG) with 10 individuals without the infection; all which were under medical release and insufficiently active. The body composition was evaluated through the DXA, as well as the cardiorespiratory aptitude through the ergometer and the strength of the upper and lower limbs through dynamometry. Both groups conducted interventions with concurrent training for 15 weeks and the interruption of exercise was evaluated after a period of 5 weeks.

Study Type

INTERVENTIONAL

Purpose

PREVENTION

Masking

NONE

Enrollment

Conditions

Lipodystrophy Syndrome, HIV Sarcopenia

Interventions

combined trainingOTHER

Combined training consisting of aerobic and resisted training in the same training session for 15 weeks followed by 5 weeks of detraining

Eligibility

Sex: ALLMin age: 18 YearsMax age: 70 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Group experience to have a diagnosis of at least 2 years living with HIV / AIDS being in clinical follow-up in the Specialized Attention Services in HIV / AIDS (SAE), using ART, TCD4 lymphocyte count equal to or greater than 500 copies / mm³, viral load Undetectable (≤ 50 copies / mm³) * Group control without any diagnosis of HIV / AIDS or any other pathology. Both groups completed the exercise program with a minimum frequency of 75%. Exclusion Criteria: * Both groups taking part in any physical exercise in time of detraining

Locations (2)

Juliany de Souza Araujo

Natal, Rio Grande do Norte, Brazil

Juliany de Souza Araujo

Parnamirim, Rio Grande do Norte, Brazil

Outcomes

Primary Outcomes

Capacity cardiorespiratory

ml (cardiorespiratory aptitude through the ergometer)

Time frame: 21 weeks

Secondary Outcomes

test force

kg (strength of the upper and lower limbs through dynamometry)

Time frame: 21 weeks

Data from ClinicalTrials.gov

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