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| ID | Type | Description | Link |
|---|---|---|---|
| NCI-2021-02624 | Registry Identifier | CTRP (Clinical Trial Reporting Program) | |
| 2019-1237 | Other Identifier | M D Anderson Cancer Center |
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IRB Study Closure
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This study assesses the performance status in stage I-III triple negative breast cancer patients who are receiving neoadjuvant chemotherapy. Information collected in this study may help doctors learn if movement and fitness trackers can be used to predict side effects in cancer patients receiving chemotherapy.
PRIMARY OBJECTIVE:
I. To determine if in-office movement trackers or baseline metabolic equivalents (METs) groups identify those patients who are at highest risk for severe adverse event (SAE)s on neoadjuvant chemotherapy.
SECONDARY OBJECTIVES:
I. To determine the association between the occurrence of SAEs, unexpected healthcare encounters, depending on the change in activity level classification between the baseline METs group and mid-treatment METs group (at month 3).
II. Explore association between patient reported outcome (PRO) data and movement tracker data.
OUTLINE:
Patients complete movement assessment 5-15 days prior to the initiation of neoadjuvant chemotherapy and at day 1 of neoadjuvant chemotherapy. Patients' SAE data is collected. Patients are observed during their neoadjuvant chemotherapy for up to 6 months.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Observational (movement assessment, medical data collection) | Patients complete movement assessment 5-15 days prior to the initiation of neoadjuvant chemotherapy and at day 1 of neoadjuvant chemotherapy. Patients' SAE data is collected. Patients are observed during their neoadjuvant chemotherapy for up to 6 months. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Behavioral Assessment | Behavioral | Complete movement assessment |
|
| Measure | Description | Time Frame |
|---|---|---|
| The number of non-hematologic serious adverse events occurring during neoadjuvant chemotherapy (i.e. correlate Microsoft motion tracking data and baseline metabolic equivalents [METs] group with incidence of serious adverse events) | Up to 6 months |
| Measure | Description | Time Frame |
|---|---|---|
| The number of severe adverse event (SAE)s | During the final 3 months of neoadjuvant chemotherapy | |
| The number of SAEs based on laboratory results | Over the final 3 months of neoadjuvant chemotherapy |
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Inclusion Criteria:
Exclusion Criteria:
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Patients with triple negative breast cancer who will receive neoadjuvant chemotherapy
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| Name | Affiliation | Role |
|---|---|---|
| Meghan Karuturi, MD | M.D. Anderson Cancer Center | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| M D Anderson Cancer Center | Houston | Texas | 77030 | United States |
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| Label | URL |
|---|---|
| MD Anderson Cancer Center | View source |
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| Electronic Health Record Review | Other | SAE data is collected |
|
| The number of SAEs based on symptoms | Over the final 3 months of neoadjuvant chemotherapy |
| The number of unexpected healthcare encounters | In the final 3 months of neoadjuvant chemotherapy |
| Correlation between patient reported outcomes (PRO) data and movement tracker data | Will calculate the Pearson correlation between PRO data and movement tracker data. Will also fit a linear mixed model with PRO data as the dependent variable and movement tracker data as covariates. Intra-subject correlation will be adjusted in linear mixed model analysis. | 6 months |
| ID | Term |
|---|---|
| D064726 | Triple Negative Breast Neoplasms |
| ID | Term |
|---|---|
| D001943 | Breast Neoplasms |
| D009371 | Neoplasms by Site |
| D009369 | Neoplasms |
| D001941 | Breast Diseases |
| D012871 | Skin Diseases |
| D017437 | Skin and Connective Tissue Diseases |
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| ID | Term |
|---|---|
| D009483 | Neuropsychological Tests |
| ID | Term |
|---|---|
| D011581 | Psychological Tests |
| D004191 | Behavioral Disciplines and Activities |
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