Fatigue and Symptom Burden in Febrile Neutropenia
This study is ongoing, but not recruiting participants.
Sponsor:
M.D. Anderson Cancer Center
Information provided by (Responsible Party):
M.D. Anderson Cancer Center
ClinicalTrials.gov Identifier:
NCT00503854
First received: July 17, 2007
Last updated: February 12, 2013
Last verified: February 2013
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Purpose
Primary Objectives:
- To determine whether fatigue improves as patients are treated for febrile neutropenia (Day #1, Day #2 and Day #6).
Secondary Objectives:
- To identify clinical factors associated in cancer patients with low risk for outpatient treatment of febrile neutropenia on either outpatient febrile neutropenia treatment pathway presenting with moderate to severe fatigue. Moderate fatigue is defined as a score of 4 through 6 on the Brief Fatigue Inventory and severe fatigue is defined as a score of 7 through 10 on the Brief Fatigue Inventory.
- To describe demographic information in cancer patients with low risk for outpatient treatment of febrile neutropenia and fatigue while enrolled in either of two outpatient febrile neutropenia treatment pathways.
| Condition | Intervention |
|---|---|
|
Solid Tumors Febrile Neutropenia |
Behavioral: Questionnaire |
| Study Type: | Observational |
| Study Design: | Observational Model: Case-Only Time Perspective: Prospective |
| Official Title: | Fatigue and Symptom Burden in Febrile Neutropenia |
Resource links provided by NLM:
Further study details as provided by M.D. Anderson Cancer Center:
Primary Outcome Measures:
- Improvement in mean fatigue level from study day 1 to day 6 [ Time Frame: 6 Days (Baseline to Day 6) ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 70 |
| Study Start Date: | May 2007 |
| Estimated Primary Completion Date: | May 2014 (Final data collection date for primary outcome measure) |
| Groups/Cohorts | Assigned Interventions |
|---|---|
| Fatique and Fever Assessment |
Behavioral: Questionnaire
Questionnaires taking about 15 to 30 minutes total.
Other Name: Survey
|
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Study Population
Patients with solid tumors at low risk for outpatient treatment of febrile neutropenia.
Criteria
Inclusion Criteria:
- Cancer patients with solid tumors at low risk for outpatient treatment of febrile neutropenia evaluated in the EC and enrolled in outpatient febrile neutropenia pathways (pathway 1 or 2). Low risk is defined as hemodynamically stable solid tumor patients that do not have pneumonia or are on steroids. Febrile neutropenia is marked by a temperature greater than or equal to 38.3 degrees Celsius and an absolute neutrophil count (ANC) less than or equal to 1000 within 24 hours.
- Patients must be able to speak, read and write in English.
- Patients must be able to complete the required survey tools independently.
- Patients must report a moderate to severe fatigue level to question # 3 of the BFI( 4 or greater on a 0-10 scale) on EC admission day.
- Pregnant women if they meet eligibility criteria of the NF pathway and are able to take the oral/IV antibiotic prescribed by th pathway.
- Patient must be greater or equal to 18 years of age.
Exclusion Criteria:
1) Patients will be excluded from the study if they are not on the neutropenic pathway at the time of study entry.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00503854
Locations
| United States, Texas | |
| UT MD Anderson Cancer Center | |
| Houston, Texas, United States, 77030 | |
Sponsors and Collaborators
M.D. Anderson Cancer Center
Investigators
| Principal Investigator: | Carmen Escalante, MD | M.D. Anderson Cancer Center |
More Information
Additional Information:
No publications provided
| Responsible Party: | M.D. Anderson Cancer Center |
| ClinicalTrials.gov Identifier: | NCT00503854 History of Changes |
| Other Study ID Numbers: | 2005-0936 |
| Study First Received: | July 17, 2007 |
| Last Updated: | February 12, 2013 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by M.D. Anderson Cancer Center:
|
Solid Tumors Febrile Neutropenia Fatigue |
Symptom Burden Questionnaire Survey |
Additional relevant MeSH terms:
|
Fatigue Fever Neutropenia Signs and Symptoms Body Temperature Changes |
Agranulocytosis Leukopenia Leukocyte Disorders Hematologic Diseases |
ClinicalTrials.gov processed this record on June 18, 2013