New study uses weekly surveys to monitor cancer Patients' symptoms remotely
NCT ID NCT05974150
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study is gathering information from 25 adults with breast, lung, ovarian, multiple myeloma, or acute myeloid leukemia who are on active treatment. Participants fill out a short online survey each week for at least 12 weeks to report how they are feeling. The goal is to build a real-world dataset that could help improve symptom monitoring and care for future patients.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could help doctors better understand and manage symptoms in real time for people with these cancers.
- What could go wrong
- This is a small, early-stage registry study (25 participants) that only collects data—it does not test a new treatment or directly improve outcomes.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 25 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2023
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
patients receiving cancer treatment for breast, lung, GI or multiple myeloma
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * All participants must be 18 years of age or older. * Subjects may be any stage and anywhere in the treatment continuum. * Subject participants must have a diagnosis of a breast, lung, AML, ovarian cancer or multiple myeloma. * Subjects must be able to complete on-line surveys using a cell phone, tablet, or computer. * All participants must be able to understand English. Exclusion Criteria: * Any patient who cannot understand written or spoken English. * Any patient without the ability to complete on-line surveys using a cell phone, tablet, or computer. * Any patient on a treatment clinical trial. * Any prisoner and/or other vulnerable persons as defined by NIH (45 CFR 46, Subpart B, C and D).
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Get notified about this study
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
4 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Cleveland Clinic Mercy Hospital
RECRUITINGCanton, Ohio, 44708, United States
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Duke
COMPLETEDDurham, North Carolina, 27707, United States
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Northshore University Health System
RECRUITINGEvanston, Illinois, 31024, United States
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Tri-County Hematology & Oncology Associates, Inc.
RECRUITINGMassillon, Ohio, 44646, United States
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Univeristy of North Carolina at Chapel Hill
COMPLETEDChapel Hill, North Carolina, 27599, United States
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University Hospitals Seidman Cancer Center
RECRUITINGCleveland, Ohio, 44106, United States
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Yale Cancer Center
COMPLETEDNew Haven, Connecticut, 06511, United States
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