New program aims to ease pain for head and neck cancer survivors
NCT ID NCT05115825
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a better pain management program for people who finished treatment for head and neck cancer. 33 survivors with ongoing pain took part. The goal was to see if the program could improve their daily physical function, mood, and overall quality of life.
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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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33 people
The number who actually took part.
- Started
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Apr 2019
- Finished
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May 2025
- 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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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: * Clinically confirmed diagnosis of HNC for which the participants have completed curative cancer treatment at the VA hospital or Oregon Health \& Science University (OHSU) within the 3-12 months following treatment * Self-reported current pain of 4 or higher, using the 0-10 Numeric Pain Rating (NRS) (0="no pain" to 10="the worst pain imaginable") * Self-report of pain 4 or higher on two occasions, more than three weeks apart, since the completion of curative treatment Exclusion Criteria: * Enrolled in hospice * Have substantial hearing or visual difficulties that would impair ability to participate * Have inadequate cognitive functioning as indicated by medical record review and/or interactions with clinical staff. If needed the investigators can follow up with the St. Louis University Mental State Examination (score of \< 22/30) (SLUMS); or * Have untreated severe psychiatric illness that would impact the ability to consent and participate in the intervention * Had only surgical treatment for their HNC
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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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OHSU Knight Cancer Institute
Portland, Oregon, 97239, United States
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Portland VA Medical Center
Portland, Oregon, 97239, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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