New program aims to help breast cancer survivors get back to work
NCT ID NCT05309265
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a new program to help breast cancer patients return to work after treatment. It includes 16 working-age women who have work difficulties. The program offers meetings and support from a team of specialists. The goal is to see if this approach is practical and helpful for patients.
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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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16 people
The number who actually took part.
- Started
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Jul 2022
- Expected to finish
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Nov 2026
An estimate. End dates often move.
- Lead sponsor
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A government agency
The lead sponsor is a government body.
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 to 67 years
- Sex
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Female participants only
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * breast cancer diagnosis (regardless of stage and treatment) * breast cancer patients in working age * breast cancer patient who will participate to an educational group session held by the physiotherapists of the PMRU * breast cancer patients with work difficulties Exclusion Criteria: * Breast cancer patients with work issues that cannot be addressed by any of the interventions (e.g., patients who would like to change their job)
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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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Azienda Unità Sanitaria Locale Reggio Emilia
Reggio Emilia, Reggio Emilia, 42123, Italy
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Other studies related to the condition(s) this trial covers.
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