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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT03320005
Other study ID # Resist protocol
Secondary ID
Status Enrolling by invitation
Phase N/A
First received August 7, 2017
Last updated October 19, 2017
Start date January 2017
Est. completion date January 2018

Study information

Verified date October 2017
Source University of Nove de Julho
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This comes from a non-randomized clinical trial, which aims to check on elderly women the effects of a program of resistance training (TR) in physical performance, in respiratory functional capacity, on health and quality of life.


Description:

Will be measured the strength of the respiratory muscles (Mip and Mep), peak expiratory flow (Peak-Flow), thoracic movements and abdominal movements, distance traveled in Incremental Shuttle Walk Test, grip strength manual, pulmonary leukocytes, biochemical parameters and indicators of quality of life and physical activity through the WHOQOL-old and IPAQ-short. The data will be tested against the distribution of the Gauss curve, by the shapiro-wilk test and, if they have a normal distribution (parametric) are expressed as mean and standard deviation, if not submit normal (non parametric) distribution will be expressed as median or range interquartílico. The first chance to compare the evolution of the group studied, will be applied to two-way ANOVA. If the distribution is abnormal, it will apply Mann-Whitney test. The multiple regression test will be used to compare the Mip and Mep with variables with the Peak-Flow, Thoracoabdominal mobility, distance traveled, immune competence, physical fitness and quality of life in the groups studied.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 25
Est. completion date January 2018
Est. primary completion date December 2017
Accepts healthy volunteers No
Gender All
Age group 60 Years and older
Eligibility Inclusion Criteria:

- 60 year old or more

- Do not have cardiac or respiratory diseases

- neurological, Musculoskeletal and other diseases preventing the practice of exercises

- not being a smoker; agree to participate in the study and signed an informed consent (IC); in the last six months preceding the evaluation did not have participated in physical activity program with the aim of improving physical performance.

Exclusion Criteria:

- Difficult to complete the tasks

- Acute diseases

- Refuse to continue the program

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Resistance training group
Resistive exercises for legs and arms

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Daysi Tobelem

Outcome

Type Measure Description Time frame Safety issue
Primary Physical performance distance traveled on ISWT Change from Baseline at 24 weeks
Secondary quality of life quality of life (WHOQOL-old) Change from Baseline at 24 weeks
Secondary respiratory muscle strength respiratory pressures Change from Baseline at 24 weeks
Secondary Hand grip Hand grip test Change from Baseline at 24 weeks
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