New app aims to ease pain for hospice patients at home
NCT ID NCT04869085
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a smartphone app called e-PainSupport for people receiving home hospice care. The app helps patients and their caregivers report pain levels to nurses and learn about pain management. Researchers wanted to see if using the app could reduce pain intensity. The study involved 88 patients, their caregivers, and nurses.
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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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88 people
The number who actually took part.
- Started
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Apr 2021
- Finished
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Jan 2024
- 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 (patient) * prior enrollment of their hospice nurse * receives analgesics for pain * speaks and reads English * age 18 or older * has a primary informal caregiver who is available for the 2 weeks of the study * expected survival of at least 2 weeks * can verbalize pain. Inclusion criteria (caregiver) * speaks and reads English * age 18 or older * cares for an enrolled patient * available for the 2 weeks of the study. Inclusion criteria (nurses participating in the RTC) * registered nurse (RN) * provides direct care to patients * has not had a prior patient enrolled in the 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.
Contacts and locations
Locations
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Rush University Medical Center
Chicago, Illinois, 60612, United States
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Other studies related to the condition(s) this trial covers.
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