Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-25 @ 4:47 AM
Ignite Modification Date: 2025-12-25 @ 4:47 AM
NCT ID: NCT05916118
Eligibility Criteria: Inclusion Criteria: 1. Receiving care at Dartmouth-Hitchcock Medical Center in Lebanon, NH 2. Age \>18 years 3. Eastern Cooperative Oncology Group Status 0 to 2; 4. Diagnosed gastrointestinal cancer of any stage 5. Scheduled to receive at least 4 cycles of oxaliplatin 6. Complete the International Physical Activity Questionnaire score equal to or greater than 99 MET minutes/week (equivalent to \~30 minutes of walking) 7. Have mediport access prior to enrollment in the study Exclusion Criteria: 1. Exercise- or mobility-limiting cardiovascular, pulmonary, musculoskeletal, or psychological disease, based on the EMR (electronic medical record) past medical history and/or based on consultation with the medical oncologist; 2. Scheduled major surgery during the study time period; 3. Pre-existing peripheral neuropathy prior to chemotherapy; 4. Patient with a history or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the trial, interfere with the subject's participation for the full duration of the trial, or is not in the best interest of the subject to participate, in the opinion of the treating investigator; 5. Prior history of treatment with oxaliplatin, docetaxel, or paclitaxel 6. Pregnant women; 7. Prisoners; 8. Inability to read or speak English/unable to consent; 9. Prognosis of less than six months
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Study: NCT05916118
Study Brief:
Protocol Section: NCT05916118