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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01768819
Other study ID # 01 - REVITA
Secondary ID
Status Completed
Phase N/A
First received January 12, 2013
Last updated January 22, 2013
Start date January 2008
Est. completion date January 2009

Study information

Verified date January 2013
Source Universidade Federal de Sao Carlos
Contact n/a
Is FDA regulated No
Health authority Brazil: Ethics Committee
Study type Interventional

Clinical Trial Summary

Although some authors have observed favorable effects of group physical activity programs, others have reported that the individualized prescription of exercises may be jeopardized by programs that do not allow sufficient consideration of individual characteristics. Therefore, we aim to verify the effects of an elderly-specific multimodal physical activity program on physical parameters after one year of intervention.


Recruitment information / eligibility

Status Completed
Enrollment 46
Est. completion date January 2009
Est. primary completion date January 2009
Accepts healthy volunteers No
Gender Both
Age group 60 Years and older
Eligibility Inclusion Criteria:

- Participate in the Geriatric Revitalization Program for one year

- Be on the waiting list for the Geriatric Revitalization Program

Exclusion Criteria:

- Attend less than 75% of the physical activity program's activities

- Absent any of the three follow-up physical parameter evaluations

Study Design

Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
Physical Activity
The intervention consisted of elderly-specific physical activity program for one year. During this period a total of 123 physical activity sessions were carried out. Each session lasted 50 minutes and included stretching, aerobic endurance exercises, resistance exercises, activities involving coordination, agility and flexibility, respiratory exercises and relaxation exercises. The sessions took place three times a week, according to American College of Sports Medicine (ACSM) recommendations. Workloads were adjusted for each subject bimonthly according to their capacity. The sessions were standardized and carried out by previously trained physical educators.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Universidade Federal de Sao Carlos

Outcome

Type Measure Description Time frame Safety issue
Primary Static Balance The one-leg stance test (OLST) was used to evaluate static balance. A point was marked at eye level on a board approximately one meter from the volunteer. Focusing on this point, the volunteer, with arms akimbo, lifted the leg of his or her choice by flexing the knee. The performance was timed with a chronometer (precision: 1ms) until either the individual lost balance or 30s was reached. The test was then carried out with the opposite leg and the series was repeated until three trials per leg had been performed. The mean time of the three trials was used for analysis. one year No
Secondary Aerobic Endurance Aerobic endurance was measured using the one-mile test or the Rockport Walking Test, which consists of having subjects walk 1,609 meters quickly, but without running. The time spent performing the task and the final heart rate were measured. one year No
Secondary Dynamic Balance A maximum-speed walking test (MSWT) was used to measure dynamic balance. A course 3.33 m long and 33.3 cm wide was marked on the floor with tape and, beginning from a standing position, the participant walked the entire course as fast as possible without running when the signal was given. Three trials were carried out; the chronometer (precision: 1ms) was started as soon as the subject's foot crossed the starting line. The mean time from the trials was used for analysis. one year No
Secondary Flexibility A sit-and-reach test (SRT) with a modified Wells flexometer (precision: 1mm) was used to evaluate the flexibility of the trunk and upper limbs. The subjects sat on the floor with their soles flush against the lower edge of the device. Then, with their overlapped hands on the upper surface touching a sliding position marker, they pushed it forward along the scale while exhaling. The best of three trials was considered the result. one year No
Secondary Handgrip Strength Handgrip Strength was measured with a JamarĀ® hydraulic hand dynamometer (Sammons Preston Roylan, Bolingbrook, IL, USA) featuring a grading scale of 0-100 Kgf (precision: 2 Kgf). The best of three trials with the dominant upper limb was selected for analysis. one year No
Secondary Body Mass Index The weight and height were measured with a calibrated analogue scale with a stadiometer. The variable of weight was measured three times and the mean value considered. Such variables were used to calculate the BMI of the volunteers. one year No
Secondary Body weight The weight was measured with a calibrated analogue scale with a stadiometer. The variable was measured three times and the mean value considered. one year No
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