App aims to ease cancer symptoms before they worsen
NCT ID NCT06396598
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether a phone app can help people with chest-area cancers and their caregivers report symptoms early and request palliative care on their own. The goal is to improve quality of life by managing pain and stress sooner. About 157 participants will use the app to log symptoms and track referrals.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 157 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2024
- Expected to finish
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Aug 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: * PATIENTS: Age ≥ 18 years * PATIENTS: Diagnosed with any stage (1-4) or type (non-small cell lung cancer, small cell lung cancer, mesothelioma, thymic carcinoma) of thoracic malignancy * PATIENTS: ≥ 2 visits at the Ohio State University Comprehensive Cancer Center (OSUCCC) Thoracic Oncology Clinic * PATIENTS: Study enrollment within 12 weeks of initial Thoracic Medical Oncology appointment * PATIENTS: Ability to understand and willingness to sign an informed consent document (or indicate approval or disapproval by another means) * PATIENTS: Ability to read and understand English * PATIENTS: Access to a device with email or text messaging capability * CAREGIVERS: Age ≥ 18 years * CAREGIVERS: Identified by patient participant as primary caregiver * CAREGIVERS: Corresponding patient participant has consented to participate in the study * CAREGIVERS: Ability to understand and willingness to sign an informed consent document (or indicate approval or disapproval by another means) * CAREGIVERS: Ability to read and understand English * CAREGIVERS: Access to a device with email or text messaging capability Exclusion Criteria: * PATIENTS: Patients who have been previously referred to ambulatory palliative care are excluded from participation * PATIENTS: Prisoners are excluded from participation * PATIENTS: Pregnant patients are excluded from participation * PATIENTS: Patients who lack capacity for medical decision-making as determined by their primary oncologist are excluded from participation * PATIENTS: There is NO exclusion criteria pertaining to Eastern Cooperative Oncology Group (ECOG) performance status, laboratory values, prior cancer diagnoses, presence of comorbidities or brain metastases
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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.
Contacts and locations
Locations
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Ohio State University Comprehensive Cancer Center
Columbus, Ohio, 43210, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.