NCT02404987
Unknown
Not Applicable
A Prospective, Observational Study, of a High Calorie and Protein Oral Nutritional Supplement, in an Older Malnourished Spanish Population
ConditionsMalnutrition
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Malnutrition
- Sponsor
- Abbott Nutrition
- Enrollment
- 224
- Locations
- 1
- Primary Endpoint
- Body Weight
- Last Updated
- 11 years ago
Overview
Brief Summary
Post-marketing observational study of a nutritional care plan, including a higher calorie, higher protein oral nutritional supplement (ONS), prescribed to Spanish patients, both free living and residing and nursing homes, who have been identified as malnourished. The objective is to assess the impact of the ONS on body weight, activities of daily living and quality of life.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Voluntarily signed and dated an informed consent form (ICF), approved by an Independent Ethics Committee (IEC)/Institutional Review Board (IRB), prior to any participation in the study.
- •Considered malnourished, or is at risk for malnutrition based on NRS 2002 score ≥
- •≥65 years of age.
- •Conforms to the requirements set forth on the study product label.
- •Under the care of a health care professional for malnutrition and has recently (within the last 7 days prior to participating in this study) been prescribed 2 servings/d of the study ONS, orally, by their health care professional.
- •Free living or residing in a nursing home.
- •Estimated, or measured, glomerular filtration rate \>60ml/min/1.73m2 (Modification of Diet in Renal Disease (MDRD) Study equation) within 60 days of beginning their nutritional care plan.
- •Body mass index (BMI) is \<30 kg/m
- •Study physician determines the subject is fit to participate.
Exclusion Criteria
- Not provided
Outcomes
Primary Outcomes
Body Weight
Time Frame: Change from baseline to 12 weeks
Secondary Outcomes
- Body Mass Index (BMI)(Change from baseline to 12 weeks)
- Katz Activities of Daily Living(Change from baseline to 12 weeks)
- Quality of Life(Change from baseline to 12 weeks)
Study Sites (1)
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