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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02434185
Other study ID # UCAM-BLD-1
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 2015
Est. completion date April 2015

Study information

Verified date October 2018
Source Universidad Católica San Antonio de Murcia
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The bilateral deficit phenomenon (BLD) is defined as an inability of the neuromuscular system to generate maximal force when two homonymous limb operate simultaneously (bilateral contraction) with respect to the force developed when both limbs acts separately (unilateral contraction). From an applied perspective, movement patterns of bilateral homonymous limb are often developed during activities of day living, e.g. rising from a chair or opening a jar. The BLD can be considered an intrinsic property of the human neuromuscular system but could be enough important to constitute a performance-limiting factor for postmenopausal women that involves a degenerative loss of muscular strength. Therefore, a specific analysis of this phenomenon and its relation with activities of daily living, such as climbing a step and rising from a chair, is crucial for detecting variables of neuromuscular performance and develop strategies to minimize the loss of strength.


Description:

- 20 postmenopausal women unexperience in strength training or resistance training, without musculoskeletal, neurological diseases, and cardiovascular limiting-diseases were recruited.

- Maximum strength of lower limbs during leg-press exercise was measured for future analysis.

- The force-time curves were measured during climbing a step and rising from a chair.

- A fragility phenotype test was applied to the subjects to determine frailty phenotype classification, including; weight loss of greater than 10 lbs in the past 12 months, maximal handgrip strength, time to walk 15-ft at usual pace, self-reported leisure time physical activity, and self-reported exhaustion.

- The anthropometric measurements were performed by dual energy X-ray absorptiometry.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date April 2015
Est. primary completion date April 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 50 Years to 70 Years
Eligibility Inclusion Criteria:

- Postmenopausal women

Exclusion Criteria:

- Unexperienced in strength training or resistance training.

- Not musculoskeletal diseases.

- Not neurological diseases.

- Not cardiovascular limiting-diseases.

- Not fragility or pre-fragility phenotype.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Spain Catholic University of Murcia Murcia

Sponsors (1)

Lead Sponsor Collaborator
Universidad Católica San Antonio de Murcia

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Assess the maximum force of lower limbs during bilateral and unilateral contraction Screening visit
Primary Assess the force-time curve during climbing a step Screening visit
Primary Assess the force-time curve during climbing rising from a chair Screening visit
Primary Assess bone mineral-free lean tissue mass by dual energy X-ray absorptiometry Screening visit
Primary Assess the fragility phenotype of the subjects Screening visit
Primary Assess the rate of force developed in time intervals (0-50, 50-100, 100-150ms) of lower limbs during bilateral and unilateral contraction Screening visit
Primary Assess fat-tissue mass and lean-tissue mass composition Screening visit
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