Correlates of CRCI and Gut Microbiome Dysbiosis; a Pilot Study
Study Details
Study Description
Brief Summary
The aim of this study is to characterize the microbiome and assess fatigue and cognition of patients with cancer undergoing standard of care treatment.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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Detailed 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.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Cancer Patients Patients diagnosed with cancer undergoing standard of care treatment. |
Outcome Measures
Primary Outcome Measures
- Characterization of fecal microbiome using molecular methods at baseline [Baseline]
Characterization of the fecal microbiome using a commercially available sampling kit and our lab's patented array for PCR at baseline
- Characterization of fecal microbiome using molecular methods at 6 months [6 months]
Characterization of the fecal microbiome using a commercially available sampling kit and our lab's patented array for PCR after 6 months of standard of care treatment.
Secondary Outcome Measures
- Cognitive Function as measured by Montreal Cognitive Assessment at baseline [Baseline]
The Montreal Cognitive Assessment (MoCA) is a rapid assessment of cognition. The MoCA-BLIND v8.1 will be used in this study as it can be administered in person as well as over the telephone. The MoCA-BLIND consists of 9 questions with the following subcategories: memory, attention, language, abstraction, delayed recall and orientation. The MoCA has been used extensively to detect cognitive impairment in many conditions, including head trauma. The MoCA will be administered by a certified tester at enrollment. Scores range from 0 to 22, higher score being a better outcome.
- Cognitive Function as measured by Montreal Cognitive Assessment at 6 months [6 months]
The Montreal Cognitive Assessment (MoCA) is a rapid assessment of cognition. The MoCA-BLIND v8.2 will be used in this study as it can be administered in person as well as over the telephone. The MoCA-BLIND consists of 9 questions with the following subcategories: memory, attention, language, abstraction, delayed recall and orientation. The MoCA has been used extensively to detect cognitive impairment in many conditions, including head trauma. The MoCA will be administered by a certified tester at enrollment. Scores range from 0 to 22, higher score being a better outcome. The MoCA will be performed after 6 months of standard of care treatment.
- Fatigue and Cognition as measured by the Fatigue and Altered Cognition Scale at baseline [Baseline]
The Fatigue and Altered Cognition Scale (FACS) is a joint project from University of Texas Medical Branch and Texas A&M University. The FACS is a 20 question assessment designed to access perceived fatigue and cognition. There are 2 subscales used to calculate a total score. The subscales are: Fatigue and Altered Cognition. The total score is calculated by adding the subscales together. The range of the total score is 0-100, with a higher score indicating more fatigue and altered cognition.
- Fatigue and Cognition as measured by the Fatigue and Altered Cognition Scale at 6 months [6 months]
The Fatigue and Altered Cognition Scale (FACS) is a joint project from University of Texas Medical Branch and Texas A&M University. The FACS is a 20 question assessment designed to access perceived fatigue and cognition. There are 2 subscales used to calculate a total score. The subscales are: Fatigue and Altered Cognition. The total score is calculated by adding the subscales together. The range of the total score is 0-100, with a higher score indicating more fatigue and altered cognition. The FACS will be performed after 6 months of standard of care treatment.
- Gastrointestinal Health measured by the Gastrointestinal Symptom Rating Scale at baseline [Baseline]
The Gastrointestinal Symptom Rating Scale (GSRS) is a specific 15-item questionnaire. Subjects are asked to numerically score their subjective symptoms on a scale of 1-7 (1 = no discomfort at all; 7 = very severe discomfort) . The sum of the scores for all 15 items is regarded as the GSRS total score. Total scores range from 15 (best outcome) to 105 (worst outcome).
- Gastrointestinal Health measured by the Gastrointestinal Symptom Rating Scale at 6 months. [6 months]
The Gastrointestinal Symptom Rating Scale (GSRS) is a specific 15-item questionnaire. Subjects are asked to numerically score their subjective symptoms on a scale of 1-7 (1 = no discomfort at all; 7 = very severe discomfort) . The sum of the scores for all 15 items is regarded as the GSRS total score. Total scores range from 15 (best outcome) to 105 (worst outcome). The GSRS will be performed after 6 months of standard of care treatment.
Eligibility Criteria
Criteria
Inclusion Criteria:
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Current diagnosis of cancer.
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Ages 18 and over.
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Has access to a device (smart phone, computer, tablet) with internet access.
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Participant is willing and able to give informed consent for participation in the study.
Exclusion Criteria:
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Females who are pregnant or lactating.
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Other medical conditions or medications deemed exclusionary by the study investigators.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | The University of Texas Medical Branch | Galveston | Texas | United States | 77555 |
Sponsors and Collaborators
- The University of Texas Medical Branch, Galveston
Investigators
- Principal Investigator: Melinda Sheffield-Moore, PhD, University of Texas
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 23-0289