Quality of Life, Sleep, and Biomarkers in People With HIV/AIDS

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

17 participants

Study Classification

INTERVENTIONAL

Study Start Date

2013-01-20

Study Completion Date

2016-09-13

Brief Summary

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Aim: Evaluate the influence of exercise, in different times, on quality of life, sleep and clinical parameters in people living with HIV/AIDS (PLHA). Methods: Intervention study, prospective.

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Detailed Description

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Aim: Evaluate the influence of exercise, in different times, on quality of life, sleep and clinical parameters in people living with HIV/AIDS (PLHA). Methods: Intervention study, prospective, a cohort with 17 PLHA participants of the exercise program, higher than 18 years, under antiretroviral therapy with CD4+ ≥ 350/mm3. Research Ethical Committee of the institution approved the study and the participants sign the informed consent and informed. All subjects underwent an exercise program in conformity to American College of Sports Medicine, 3 times per week during 40 minutes. Were evaluated the quality of life (QoL) with the Quality of Life - HAT - QoL and the sleep quality (SQ) with the Pittsburg questionnaire. The subjects were evaluated before the start of exercise program and in three times: short-term (2 to 4 months), medium-term (between 5 and 17 months) and long-term (between 18 to 25 months).

Conditions

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HIV/AIDS and Infections Disorder Sleep Lipodystrophy

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Intervention study, prospective, a cohort with 17 PLHA participants of the exercise program

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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Aerobic, resistance and concorrent

The group underwent exercise program with protocols of resistance training, aerobic training and concurrent training, with frequency of three times per week.

Group Type EXPERIMENTAL

Aerobic, resistance and concorrent.

Intervention Type OTHER

All protocols followed the American College of Sports Medicine (ACSM) guidelines , with frequency of three times per week, duration between 40-50 minutes, low to high intensity, modified according to the physical needs of each participant, respecting the physical training principles.

Interventions

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Aerobic, resistance and concorrent.

All protocols followed the American College of Sports Medicine (ACSM) guidelines , with frequency of three times per week, duration between 40-50 minutes, low to high intensity, modified according to the physical needs of each participant, respecting the physical training principles.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Must have age ≥ 18 years old;
* diagnosis of HIV/AIDS;
* use of antiretroviral therapy;
* Must have lymphocyte T CD4+ cell count ≥ 350 cel/mm3
* Must have physical fitness by the assistant physician.