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Correlates of CRCI and Gut Microbiome Dysbiosis; a Pilot Study

The University of Texas System (UT) logo

The University of Texas System (UT)

Status

Enrolling

Conditions

Cancer

Study type

Observational

Funder types

Other

Identifiers

NCT06098404
23-0289

Details and patient eligibility

About

The aim of this study is to characterize the microbiome and assess fatigue and cognition of patients with cancer undergoing standard of care treatment.

Full description

Cancer-related fatigue is experienced by nearly all patients during treatment, and cancer-related cognitive impairment (CRCI), which is a decrease in neurocognitive functioning that can be caused by cancer or its treatment, is present in up to ¾ of patients during treatment. Fatigue and CRCI have both been linked to the composition of the gut microbiome in cancer patients. CRCI is often reported as one of the most debilitating and life-altering aspects of cancer and treatment. Although CRCI is widely reported in patients with a variety of cancers and undergoing a variety of treatments, it is not clear if the mechanisms leading to symptoms are the same throughout. Using identical methods to monitor CRCI symptoms and microbial dysbiosis in a cross-section of various cancers, cancer stages, and treatments, can help to identify commonalities associated with symptoms.

Specific Aims

Specific Aim 1: Characterize the microbiome of cancer patients and compare to healthy control subjects from previous studies.

Specific Aim 2: Assess fatigue in cancer patients and determine associations with composition of the gut microbiome.

Enrollment

250 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Current diagnosis of cancer.
  2. Ages 18 and over.
  3. Has access to a device (smart phone, computer, tablet) with internet access.
  4. Participant is willing and able to give informed consent for participation in the study.

Exclusion criteria

  1. Females who are pregnant or lactating.
  2. Other medical conditions or medications deemed exclusionary by the study investigators.

Trial design

250 participants in 1 patient group

Cancer Patients
Description:
Patients diagnosed with cancer undergoing standard of care treatment.

Trial contacts and locations

1

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Central trial contact

Kristen McGovern, PhD; Kate Randolph, BS

Data sourced from clinicaltrials.gov

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