PACTIVEM: Evaluation Study of Interventions for Physical Activity Promotion in Primary Health Care in Brazil.

Sponsor
University of Sao Paulo (Other)
Overall Status
Completed
CT.gov ID
NCT01852981
Collaborator
Fundação de Amparo à Pesquisa do Estado de São Paulo (Other), Conselho Nacional de Desenvolvimento Científico e Tecnológico (Other)
157
2
3
20
78.5
3.9

Study Details

Study Description

Brief Summary

To verify changes in physical activity levels, metabolic markers, and physical fitness as results of two physical activity interventions within the Brazilian public health system (primary health care).

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Lifestyle counseling
  • Behavioral: Supervised exercise
N/A

Detailed Description

The effects of two strategies - lifestyle counseling focused on physical activity, and supervised exercise - adapted to the Brazilian primary health care system and resources will be compared between them and with a control group. Subjects are healthy, physically inactive adults from a low socioeconomic area of Sao Paulo city. Evaluations will be done at the study baseline, 6 months, 12 months, and 18 months (6 months follow-up) after the beginning. The primary outcome is leisure-time physical activity.

Study Design

Study Type:
Interventional
Actual Enrollment :
157 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Evaluation Study of Interventions for Physical Activity Promotion in Primary Health Care/Health Family Strategy in Brazil.
Study Start Date :
Feb 1, 2011
Actual Primary Completion Date :
Feb 1, 2012
Actual Study Completion Date :
Oct 1, 2012

Arms and Interventions

Arm Intervention/Treatment
Experimental: Lifestyle counseling

Physical activity promotion using methods based on health education.

Behavioral: Lifestyle counseling
Strategies consisted of group discussion, some physical activities, phone support, and printed materials. The content and strategies were elaborated by a team formed by a doctor, nutritionists, a psychologist, and physical education professionals and the main aim was to promote the engagement in physical activity, working not only on behavioral change but also on the environment attributes available for physical activity practice. The main strategy was the group discussion, which sessions lasted 120 minutes each and its frequency changed as follow: in the first month they were weekly; in the second occurred twice per month; and in the third month onwards sessions were monthly. All sessions occurred in the Primary Health Unit or inside a community association building.

Experimental: Supervised exercise

Supervised sessions of aerobic, strength, and stretching exercises, drawn up in accordance to the American College of Sports Medicine recommendations.

Behavioral: Supervised exercise
Supervised exercise program in groups. Individuals in this program participated in three weekly structured and supervised sessions of aerobic, strength, and stretching exercises, drawn up in accordance to the American College of Sports Medicine recommendations. Load, intensity, and exercise adjustments were made during the program. All sessions lasted 60 minutes each and occurred in a gymnasium nearby the Primary Health Unit.

No Intervention: Control

Control group.

Outcome Measures

Primary Outcome Measures

  1. Change from baseline leisure-time physical activity at 12 months [12 months]

  2. Change from baseline leisure-time physical activity at 18 months [18 months]

Secondary Outcome Measures

  1. Change from baseline leisure-time physical activity at 6 months [6 months]

  2. Change from baseline transport-related physical activity at 12 months [12 months]

  3. Change from baseline transport-related physical activity at 6 months [6 months]

  4. Change from baseline transport-related physical activity at 18 months [18 months]

  5. Change from baseline quality of life at 12 months [12 months]

  6. Change from baseline quality of life at 18 months [18 months]

  7. Change from baseline physical fitness at 12 months [12 months]

  8. Change from baseline physical fitness at 18 months [18 months]

  9. Change from baseline body composition at 12 months [12 months]

  10. Change from baseline body composition at 18 months [18 months]

  11. Change from baseline blood pressure at 12 months [12 months]

  12. Change from baseline blood pressure at 18 months [18 months]

  13. Change from baseline blood glucose at 12 months [12 months]

  14. Change from baseline blood glucose at 18 months [18 months]

  15. Change from baseline blood lipids at 12 months [12 months]

  16. Change from baseline blood lipids at 18 months [18 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • 18 years old or more;

  • To be registered in the Brazilian public health system.

Exclusion Criteria:
  • Practice of leisure-time physical activity in the previous month;

  • Practice of transport-related physical activity (walking or cycling) for at least 150 minutes in the previous week;

  • Diagnostic of type II diabetes or severe arterial hypertension;

  • Use of beta-blockers for treating hypertension or cardiovascular disease;

  • Health problem or disease that would make the individual incapable of leaving home and making the journey to practice physical activity;

  • Diseases such as cancer, cirrhosis, chronic kidney disease, chronic obstructive pulmonary disease osteoporosis and severe depression at advanced stages;

  • Cognitive problem or disease that would not allow the individual from answering the questionnaire alone;

  • Being morbidly obese, with a body mass index (BMI) ≥40 kg/m2;

  • To have plans to move house over the two-year subsequent period;

  • Being pregnant.

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Sao Paulo Sao Paulo SP Brazil 03828000
2 School of Arts, Sciences and Humanities, University of Sao Paulo Sao Paulo Brazil

Sponsors and Collaborators

  • University of Sao Paulo
  • Fundação de Amparo à Pesquisa do Estado de São Paulo
  • Conselho Nacional de Desenvolvimento Científico e Tecnológico

Investigators

  • Principal Investigator: Alex A Florindo, Ph.D., University of Sao Paulo

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
Alex Antonio Florindo, Ph.D., University of Sao Paulo
ClinicalTrials.gov Identifier:
NCT01852981
Other Study ID Numbers:
  • 2009/14119-4
  • NCT01330836
First Posted:
May 14, 2013
Last Update Posted:
May 14, 2013
Last Verified:
May 1, 2013
Keywords provided by Alex Antonio Florindo, Ph.D., University of Sao Paulo

Study Results

No Results Posted as of May 14, 2013