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A Randomized Controlled Trial of Hesperidin for Improving Cognitive Function in Overweight and Obese Middle-Aged and Older Adults

Status: Recruiting
Location: See location...
Intervention Type: Dietary supplement
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

A randomized, double-blind, placebo-controlled trial was designed to test whether two doses of hesperidin (a natural flavonoid from citrus fruits) improve cognitive function in overweight and obese older adults. A total of 105 participants, aged 55-75 years with a BMI ≥24 kg/m² or elevated waist circumference, will be randomly assigned to one of three 10-week treatments: placebo, low-dose hesperidin (300 mg/day), or high-dose hesperidin (600 mg/day). The primary aim is to see if hesperidin supplementation enhances cognitive performance - specifically executive function, memory, and attention - and to explore any dose-response relationship. Secondary aims include examining changes in gut microbiota composition and related metabolites, as well as exploring potential mechanisms behind any observed effects. The findings are expected to provide scientific evidence on whether hesperidin could serve as a nutritional strategy to support cognitive health in this population.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 55
Maximum Age: 75
Healthy Volunteers: f
View:

• Age 55-75 years

• BMI ≥ 24 kg/m² or waist circumference ≥ 90 cm (men) / ≥ 85 cm (women)

• Willing to participate and sign informed consent

Locations
Other Locations
China
Community Health Centers in Shanghai
RECRUITING
Shanghai
Contact Information
Primary
Min Hou
minhou@sjtu.edu.cna
13121858610
Backup
ShiQi Lin
olinalin@sjtu.edu.cn
18616825727
Time Frame
Start Date: 2026-02-01
Estimated Completion Date: 2027-03-30
Participants
Target number of participants: 105
Treatments
Placebo_comparator: Placebo Group
Participants receive 2 placebo capsules (corn starch 600 mg/day) daily for 10 weeks. Capsules are identical in appearance, smell, and packaging to hesperidin capsules.
Experimental: Low-Dose Hesperidin Group
Participants receive hesperidin 300 mg + corn starch 300 mg (total 600 mg) daily, taken as 2 capsules for 10 weeks.
Experimental: High-Dose Hesperidin Group
Participants receive hesperidin 600 mg daily, taken as 2 capsules for 10 weeks.
Related Therapeutic Areas
Sponsors
Leads: Min Hou

This content was sourced from clinicaltrials.gov

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