Lipodystrophy Syndrome, HIV, Sarcopenia
Conditions
Keywords
Detraining, Physical aptitude, HIV
Brief summary
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).
Detailed description
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.
Interventions
OTHERcombined training
Combined training consisting of aerobic and resisted training in the same training session for 15 weeks followed by 5 weeks of detraining
Sponsors
Universidade Federal do Rio Grande do Norte
Study design
Intervention model
SEQUENTIAL
Primary purpose
PREVENTION
Masking
NONE
Intervention model description
This is a longitudinal study of the non-randomized experimental type, presenting a non-probabilistic sample for convenience and independent groups. The sample consisted of 21 individuals divided into 2 groups: Experimental Group (EG) and Control Group (CG). The EG was composed of 11 people living with HIV/AIDS and CG composed of 10 people with no infection
Eligibility
Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes
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
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Capacity cardiorespiratory | 21 weeks | ml (cardiorespiratory aptitude through the ergometer) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| test force | 21 weeks | kg (strength of the upper and lower limbs through dynamometry) |
Other
| Measure | Time frame | Description |
|---|---|---|
| body composition | 21 weeks | kg (body composition was evaluated through the DXA) |
Countries
Brazil
Outcome results
None listed