Actively Recruiting

Phase Not Applicable
Age: 40Years - 65Years
FEMALE
ID07097155

Effect of Daily Avocado Consumption on Cellular Aging in Female Breast Cancer Survivors: The ACCA Study

Led by Institut Investigacio Sanitaria Pere Virgili · Updated on 2026-05-12

120

Participants Needed

1

Research Sites

21 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying women who have survived breast cancer to understand how eating one avocado daily might affect biological aging, measured by the length of telomeres. The study focuses on breast cancer survivors aged 40 to 65, exploring whether dietary changes can influence aging markers and other health indicators such as inflammation, oxidative stress, cardiovascular markers, mental health symptoms, quality of life, and diet quality. This is a randomized controlled trial aiming to compare avocado consumption to a habitual diet with low avocado intake. Participants will be randomly assigned to one of two groups: an intervention group that will consume one avocado daily for four months alongside their usual diet, and a control group that will continue their usual diet without encouragement to eat avocados. Avocados will be provided free of charge to the intervention group every two weeks, supported by recipe leaflets to help incorporate avocados into their meals. The control group will maintain their regular diet without specific dietary changes. During the study, participants will complete questionnaires, provide blood and urine samples, and undergo measurements like blood pressure and body size assessments at the start and end of the four-month period. Researchers will evaluate changes in telomere length as the primary outcome, alongside secondary measures including telomerase activity, inflammation, oxidative stress, cardiovascular markers, mental health symptoms, quality of life, and diet. The study aims to understand the potential impact of avocado intake on cellular aging and overall health in breast cancer survivors.

CONDITIONS

Brief Title

Avocado Consumption and Cellular Aging in Breast Cancer Survivors

Who Can Participate

Age: 40Years - 65Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Women diagnosed with primary breast cancer in stages I, II or III
  • Aged 40 to 65 years at screening
  • Completed cancer treatment (radiotherapy and chemotherapy) at least 6 months ago but not more than 10 years ago
  • Currently consume fewer than 2 avocados per week
  • Signed informed consent
Not Eligible

You will not qualify if you...

  • Metastasis
  • Ductal carcinoma or lobular carcinoma in situ
  • Breast cancer recurrence
  • Cancer diagnosis other than breast cancer or non-melanoma skin cancer
  • Body mass index greater than or equal to 40 kg/m2
  • Currently pregnant, breastfeeding, or planning pregnancy within 6 months
  • Allergy to latex
  • Unwilling to consume avocado
  • Immunodeficiency or HIV-positive status
  • Alcohol abuse (more than 50 g/day)
  • Unstable use of certain supplements or plans to change use during the study
  • Currently in another randomized controlled trial
  • Difficulty or inability to follow study procedures adequately
  • Inability or unwillingness to give written informed consent or communicate with study staff
  • Acute infection or inflammation unless recovered for at least 3 months prior to participation

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 4 months

Participants follow their usual diet and consume one avocado per day for 4 months. Avocados are provided and picked up every two weeks from the study site.

Biweekly visits to pick up avocados

Trial Site Locations

Total: 1 location

1

Unit for Public Health and Nutritional Epidemiology, Faculty of Medicine and Health Sciences, Universitat Rovira i Virgili

Reus, Tarragona, Spain, 43201

Actively Recruiting

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Research Team

N

Nerea Becerra Tomás, PhD

V

Victoria Arija, Professor

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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