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Dietary Wild Blueberries and Joint Health

Nevada System of Higher Education (NSHE) logo

Nevada System of Higher Education (NSHE)

Status

Not yet enrolling

Conditions

Pain Assessment
Gut -microbiota
Inflammation Biomarkers
Joint Pain

Treatments

Dietary Supplement: Wild blueberry
Dietary Supplement: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT06828159
OMRF WB01
WBANA01 (Other Grant/Funding Number)

Details and patient eligibility

About

The goal of this proposed study is to examine the effects of dietary wild blueberries on gut microbiome, serum markers of inflammation, and joint function in adults. Each participant will consume 25g freeze-dried blueberries or matched placebo powder for 12 weeks, with a 2-week washout phase between.

Enrollment

50 estimated patients

Sex

All

Ages

40 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adults with documented multi-joint/knee arthritis

Exclusion criteria

  • inability to give informed consent
  • pregnancy or lactation
  • planned knee replacement surgery
  • allergy or contraindication to berries
  • recent trauma of the knee responsible of the symptomatic knee
  • intra-articular injection in the target knee/hip in the last 3 months
  • oral corticosteroid therapy ≥ 5 mg/day (prednisone equivalent) at baseline
  • use of berry extracts in the last 3 months
  • special diets
  • cancer treatment
  • bone diseases

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

50 participants in 2 patient groups, including a placebo group

Wild blueberries
Experimental group
Description:
25g freeze-dried wild blueberries daily for 12 weeks
Treatment:
Dietary Supplement: Wild blueberry
Placebo
Placebo Comparator group
Description:
Placebo powder free from polyphenols matched for calories
Treatment:
Dietary Supplement: Placebo

Trial contacts and locations

0

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Central trial contact

Arpita Basu

Data sourced from clinicaltrials.gov

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