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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02909062
Other study ID # 16-493
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 2016
Est. completion date August 21, 2020

Study information

Verified date August 2020
Source Memorial Sloan Kettering Cancer Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Electronic activity monitoring (EAM) devices are wearable electronic devices that monitor functional activity and provide personal feedback on activity progression. This study aims to determine if EAM can provide an objective, assessment of patient functional activity. The study will also examine the change in functional activity experienced by patients during the first cycle of chemotherapy. Another objective of the study will be to see if baseline functional activity and the change in functional activity that occurs during the first cycle of chemotherapy can be used to predict patient tolerability of subsequent cycles of chemotherapy.


Recruitment information / eligibility

Status Completed
Enrollment 54
Est. completion date August 21, 2020
Est. primary completion date August 21, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Clinical diagnosis of gastrointestinal malignancy.

- Age = 18 years

- Planned to receive systemic chemotherapy, either adjuvant chemotherapy, or neoadjuvant chemotherapy, or any new line of chemotherapy in the setting of advanced disease. Subjects may enroll prior to chemotherapy or during the first cycle of treatment.

Exclusion Criteria:

- Restricted mobility defined as dependence or anytime use of a walker or wheelchair in the past three months.

- Refusing systemic chemotherapy.

- Concurrent radiotherapy with chemotherapy

- Have received at least one cycle of chemotherapy in the current chemotherapy regimen.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Electronic Activity Monitoring (EAM)
All registered patients will receive a wearable EAM device that will measure their physical activity. Patients will wear this device around their wrist for the designated period of assessment. The EAM device has the potential to measure active minutes, number of steps, distance walked and number of floors climbed. For the purpose of this study the EAM data captured will focus on daily step count.
Behavioral:
Daily Questionnaire
Participants will be asked to complete this self-administered, paper-based questionnaire each day that they are expected to wear the EAM device. The questionnaire was designed specifically for the purpose of this study. It consists of 5 items that ask about the patient's perceived level of physical activity and fatigue in each 24 hour period that they have worn the EAM device. The daily questionnaires will be optional; however each participant will be encouraged to complete them.

Locations

Country Name City State
United States Memorial Sloan Kettering Cancer Center Basking Ridge New Jersey
United States Memorial Sloan Kettering Commack Commack New York
United States Memorial Sloan Kettering Westchester Harrison New York
United States Memorial Sloan Kettering Monmouth Middletown New Jersey
United States Memorial Sloan Kettering Cancer Center New York New York
United States Memorial Sloan Kettering Rockville Centre Rockville Centre New York

Sponsors (1)

Lead Sponsor Collaborator
Memorial Sloan Kettering Cancer Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary EAM Max Step-count On-Chemotherapy - EAM Max Step-count Pre-Chemotherapy change in physical activity between pre-chemotherapy and on-chemotherapy by counting the steps 1 year
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