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N/A Completed N=543 Randomized Quadruple-blind Prevention

Encapsulated Juice Powder Concentrate for Preventing Common Cold Symptoms

Source: ClinicalTrials.gov NCT00778648 ↗
Enrolled (actual)
543
Serious AEs
0.0%
Results posted
Oct 2010
Primary outcomePrimary: Number of Days With at Least Moderate (i.e. Moderate or Severe) Common Cold Symptoms. — 7.6; 9.5 Number of days — p=0.023

Summary

The primary objective of this study is to determine the effect of an encapsulated juice powder concentrate on the number of days with at least moderate common cold symptoms over winter time.

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Days With at Least Moderate (i.e. Moderate or Severe) Common Cold Symptoms.
7.6; 9.5 0.023 sig
SECONDARY
Secondary Endpoints of This Study Are Mean Health-related Quality of Life, Mean Common Cold Related Total Costs, Direct and Indirect (Productivity Loss) Costs

Eligibility Criteria

Inclusion Criteria

  • Female or male, 18-65 years of age.
  • Able and willing to take the active or placebo capsules over the whole study period.
  • Health care professionals with essential patient contact (physicians, nurses, physiotherapists, etc) in Berlin, Germany.
  • Written informed consent.

Exclusion Criteria

  • Known or suspected hypersensitivity or allergy to one of the ingredients of Juice Plus+®.
  • Refusal to stop intake of additional vitamin supplements during study.
  • Pregnancy or Lactation.
  • Alcohol addiction, drug abuse or any other condition considered by the investigator to interfere with study procedures.
  • Language limitations regarding interviews and questionnaires.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00778648). 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. Informational only — not medical advice.

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