- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03871582
Number of Meals With Adequate Protein Intake and Functionality in Middle to Older Aged Mexican Adults
Study Overview
Detailed Description
Dietary protein intake per meal was assessed with 24-h dietary recalls to determine the number of meals with adequate protein intake (>30 g, >0.4 g/kg). Functionality was assessed with self-reported questionnaires about daily living activities (Barthel), and instrumental activities of daily living (Lawton). Subjects were categorized according the number of meals with adequate protein intake (zero meals, one meal, two or three meals), and their functionality score for both questionnaires (high, middle, and low scores).
With multinomial logistic regression, the investigators assessed if consuming zero or one meal with adequate protein intake could be associated with lower functionality in comparison with consuming two or three meals with enough protein. The logistic regression was adjusted for covariables (age, sex, BMI categories for the elderly, number of diagnosed diseases, inadequate protein intake per day [<1.2 g/kg/d]).
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Jalisco
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Guadalajara, Jalisco, Mexico, 44430
- Instituto de Ciencias Aplicadas a la Actividad Física y al Deporte
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Subjects able to stand up and walk independently or with walking sticks only.
- Subjects able to answer questionnaires independently or with minimum caregivers' assistance
Exclusion Criteria:
- Subjects reporting any kind of hospitalization within the last year.
Study Plan
How is the study designed?
Design Details
- Observational Models: Other
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Participants
Middle to older aged (>50 years) Mexican adults attending to the Geriatrics Department from the Western General Hospital (Zapopan, Jalisco,Mexico).
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Cross-sectional
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Functionality on Instrumental Activities of Daily Living - Lawton questionnaire
Time Frame: One day
|
Functionality score for instrumental activities of daily living (assessed with Lawton questionnaire).
This instrument assess how well the subject perform some daily activities involving tools (e.g.
handling finances, taking medication, using the telephone).
The instrument consists on five items for men and eight for women, and each item is coded for 0 or 1 depending on if subjects are capable to successfully complete the activity.
Therefore, the score ranges from 0 to 5 in men and 0 to 8 in women, the higher the score, the more functional the subj
|
One day
|
Functionality on Activities of Daily Living - Barthel questionnaire
Time Frame: One day
|
Functionality score for activities of daily living (assessed with Barthel questionnaire).
This instrument assess how well the subject perform some daily activities (e.g.
dressing, using stairs).
The instrument consists on ten items for both men and women coded as 0 or multiples of 5 (i.e. 5, 10, 15) depending on if subjects are capable to successfully complete the activity.
The score ranges from 0 to 100 for both men and women, the higher the score, the more functional the subject.
|
One day
|
Collaborators and Investigators
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- HGO-ICAAFYD18-3
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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