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Spots Global Cancer Trial Database for Sleep Architecture and Chemotherapy-Related Fatigue

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Trial Identification

Brief Title: Sleep Architecture and Chemotherapy-Related Fatigue

Official Title: Sleep Architecture and Chemotherapy-Related Fatigue

Study ID: NCT00178204

Interventions

Study Description

Brief Summary: The purpose of this study is to identify specific chemotherapy-related changes in sleep stages/architecture that may relate to an increase in fatigue in individuals with cancer. The researchers hypothesize that the fatigue experienced by cancer patients receiving chemotherapy is in part due to changes in restorative sleeping during the non-rapid eye movement cycles of sleep (i.e., delta activity).

Detailed Description: Studies have shown a strong positive correlation between self-reported changes in sleep and cancer patients' fatigue, and also between an objective measure of sleep continuity, \[i.e., actigraphy and polysomnography (PSG)\] and self-reported fatigue. Chemotherapy disrupts normal sleep patterns, and fatigue, in the later stages of chemotherapy, may occur as a result of disturbed nocturnal sleep continuity. However, the causes of chemotherapy-related fatigue remain unknown, and whether or not abnormal sleep architecture contributes to this debilitating effect has yet to be explored. We believe that fatigue experienced by many cancer patients receiving chemotherapy is due, at least in part, to changes in delta activity \[i.e., restorative sleep during the non-rapid eye movement (NREM) cycles of sleep\]. A finding that slow wave sleep abnormalities play a significant role in fatigue would prompt further confirmatory studies and support controlled intervention studies. Comparisons: In a clinical trial of individuals with cancer prior to, during, and after completion of chemotherapy, we will identify and compare specific chemotherapy-related changes in sleep stages/architecture that may relate to an increase in fatigue. These changes will be measured by actigraphy, PSG, and patient self-reporting techniques (e.g., sleep diaries, questionnaires). The primary objective is to: * examine the role of delta sleep in the development of chemotherapy-induced fatigue in cancer patients Secondary objectives are to: * characterize the involvement of other elements of sleep architecture \[e.g., rapid eye movement (REM) sleep\] and changes in sleep continuity relating to the development of chemotherapy-induced fatigue in cancer patients * examine the role of sleep architecture in the persistence of chemotherapy-induced fatigue * examine (in post hoc analyses) the relationship of various physical symptoms and patient variables that may be related to fatigue (e.g., pain, hot flashes, anxiety, hemoglobin, menopausal status, sleep continuity, and QOL) and to each other, both during and following chemotherapy. Answers to these questions will provide information that will be helpful in developing potential targets for interventions to reduce fatigue.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

University of Rochester James P. Wilmot Cancer Center, Rochester, New York, United States

Contact Details

Name: Joesph A Roscoe, Ph.D.

Affiliation: University of Rochester

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

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