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Phase 3 N=17 Randomized Double-blind Prevention

Curcumin and Function in Older Adults

Older Adults · Physical Function · Cognitive Function

Enrolled (actual)
17
Serious AEs
0.0%
Results posted
Feb 2022
Primary outcome: Primary: Curcumin and Physical Function -Walking — 0.014; 0.103 meters/second

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
Curcumin (Drug); microcrystalline cellulose (Drug)
Age
Older Adult · 65+ yrs
Sex
All
Sponsor
University of Florida
Primary completion
Oct 2019

Outcome Measures

OutcomeResultp-value
PRIMARY
Curcumin and Physical Function -Walking
0.014; 0.103
PRIMARY
Curcumin and Physical Function - Hand Grip
0.63; -0.25
SECONDARY
Curcumin and Cognitive Function - Attention & Memory
0.33; -2.75
SECONDARY
Curcumin and Pain
0.97; 1.3; 0.2; 1.6
SECONDARY
Curcumin and Inflammation - Interleukin-6
3.1; 2.7; 3.4; 3.6

Summary

This placebo-controlled RCT tests whether dietary supplementation with curcumin maintains or improves cognitive and physical function in older adults who are at high risk of functional decline due existing (mild) functional impairments and elevated biomarkers of inflammation and explore the association between functional changes and changes in biological indicators of active inflammation.

Eligibility Criteria

Inclusion Criteria

  • Age > 65 years
  • Usual walking speed 0.44 m/sec on the 4 m walk
  • Sedentary lifestyle ( 1.0 mg/dL
  • Willingness and ability to give informed consent
  • Willingness to be randomized to the intervention groups
  • Availability for participation through duration of study

Exclusion Criteria

Exclusion Criteria (General)

  • Unable to complete 400 meter walk test
  • Failure or inability to provide informed consent
  • Residence in a Skilled Nursing Facility (SNF); residence in an Assisted Living Facility (ALF) or independent housing is allowed
  • Self-reported inability to walk one block
  • Blood pressure readings >160/100
  • Significant cognitive impairment, defined as a known diagnosis of dementia, or a Mini-Mental State Exam (MMSE) score 20)
  • Severe cardiac disease, including NYHA Class III or IV congestive heart failure, clinically significant aortic stenosis, history of cardiac arrest, use of a cardiac defibrillator, or uncontrolled angina
  • Severe pulmonary disease, pneumonitis or interstitial lung disease
  • Severe rheumatologic or orthopedic diseases (e.g., awaiting joint replacement, active inflammatory disease)
  • Neurological conditions that cause impaired muscle function or mobility (e.g., Parkinson's Disease, multiple sclerosis, ALS)
  • Other significant co-morbid medical disease (e.g. renal failure with eGFR < 30 ml/minute or on hemodialysis) or severe psychiatric disorder (e.g. bipolar, schizophrenia)
  • Terminal illness with life expectancy less than 12 months, as determined by a physician
  • Excessive alcohol use, defined as more than 5 drinks/day for males or more than 4 drinks/day for females, or more than 14 drinks per week
  • Current smoker or less than 3 years smoking cessation
  • Participating in another clinical trial or receiving an investigational product within 3 months prior to screening/enrollment

Exclusion Criteria (Curcumin-related)

  • Diabetes mellitus currently taking medications to lower blood glucose (oral or by injection)
  • Current use of anticoagulant or anti-platelet medications (aspirin 81 mg daily is allowed)
  • Congenital or acquired bleeding disorders
  • Cholelithiasis or other gall bladder or biliary tract disease
  • Chronic gastrointestinal blood loss or iron deficiency (serum ferritin < 12 ng/mL, with or without anemia)
  • History of estrogen-sensitive conditions including breast, uterine, and ovarian cancers; endometriosis; and uterine fibroids
  • History of Tuberculosis (TB), HIV, Hepatitis B or C, or other disease potentially compromising immune function
  • Current use of medications targeting immune or inflammatory function (e.g., sulfasalazine)
  • Current use of anabolic medications (i.e., growth hormones or testosterone), antidepressant medications and antipsychotic agents (including monoamine oxidase inhibitors), or anticholinesterase inhibitors (i.e., Aricept)

Temporary Exclusion Criteria

  • Acute infection (urinary, respiratory, other) or hospitalization within 1 month
  • Myocardial infarction, CABG, or valve replacement within past 6 months
  • Pulmonary embolism or deep venous thrombosis within past 6 months
  • Stroke, hip fracture, hip or knee replacement, or spinal surgery within past 4 months
  • Receiving physical therapy for gait, balance, or other lower extremity training
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03085680). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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