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

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Brief Title

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

Official Title

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

Brief Summary

      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.

Detailed Description

      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).

Study Type

Interventional

Primary Outcome

Quality of life

Secondary Outcome

 Quality of sleep

Condition

HIV/AIDS and Infections

Intervention

Aerobic, resistance and concorrent.

Study Arms / Comparison Groups

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

Publications

* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.

Recruitment Information

Recruitment Status

Other

Estimated Enrollment

17

Start Date

January 20, 2013

Completion Date

September 13, 2016

Primary Completion Date

April 22, 2015

Eligibility Criteria

        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.

        Exclusion Criteria:

          -  pregnancy;

          -  severe hearing deficiency.

Gender

All

Ages

18 Years - 60 Years

Accepts Healthy Volunteers

No

Contacts

RAFAELA MEDEIROS, ,

Administrative Informations

NCT ID

NCT03445351

Organization ID

AFISA

Responsible Party

Sponsor-Investigator

Study Sponsor

JULIANY DE SOUZA ARAUJO

Study Sponsor

RAFAELA MEDEIROS, Principal Investigator, Universidade Federal do Rio Grande do Norte

Verification Date

February 2018