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| ID | Type | Description | Link |
|---|---|---|---|
| UMCC 2013.073 | Other Identifier | University of Michigan Cancer Center |
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| Name | Class |
|---|---|
| Damon Runyon Cancer Research Foundation | OTHER |
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Many breast cancer survivors report chronic pain that develops or worsens following chemotherapy. The impact of chemotherapy on the development of chronic pain is uncertain. In this proposal, we are studying the impact of chemotherapy on a patient's sensitivity to pain. We are also investigating whether a patient's sensitivity to pain is related to how many symptoms she experiences during treatment.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Adjuvant chemotherapy | Subjects will undergo pain testing, then receive standard of care chemotherapy, and then undergo pain testing. |
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| Measure | Description | Time Frame |
|---|---|---|
| Feasibility of recruiting patients at chemotherapy initiation | Feasibility will be measured by the proportion of women who complete the post-chemotherapy assessment among those consenting to participate in the trial. | 15 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Change in Pain Sensitivity in Breast Cancer Patients Associated with Chemotherapy | Patients will undergo quantitative sensory testing to identify change in pain threshold and in the magnitude of conditioned pain modulation before chemotherapy and shortly after the final dose of chemotherapy. | 15 weeks |
| Association Between Baseline Pain-Pressure Threshold and Development of Chemotherapy-associated Acute Pain |
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Inclusion Criteria:
Exclusion Criteria:
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Women initiating adjuvant chemotherapy to treat stage I-III breast cancer.
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| Name | Affiliation | Role |
|---|---|---|
| Norah L Henry, MD, PhD | University of Michigan | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Michigan Health System | Ann Arbor | Michigan | 48109 | United States |
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| ID | Term |
|---|---|
| D001943 | Breast Neoplasms |
| D059350 | Chronic Pain |
| ID | Term |
|---|---|
| D009371 | Neoplasms by Site |
| D009369 | Neoplasms |
| D001941 | Breast Diseases |
| D012871 | Skin Diseases |
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Exploratory analyses will be conducted to examine associations between either baseline or change in quantitative sensory testing measures and change in patient-reported outcomes. |
| 15 weeks |
| D017437 |
| Skin and Connective Tissue Diseases |
| D010146 | Pain |
| D009461 | Neurologic Manifestations |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |