Psychosocial Support to Facilitate the Return to Employment of Women With Breast Cancer (NCT01780064) | Clinical Trial Compass
TerminatedNot Applicable
Psychosocial Support to Facilitate the Return to Employment of Women With Breast Cancer
Stopped: Lack of enrollment
France128 participantsStarted 2013-02
Plain-language summary
The purpose of this study is to compare the effect of early individualized psychosocial assets versus a standard support on social inequalities in the rate of return to work
Who can participate
Age range
18 Years – 65 Years
Sex
FEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Women ≥ 18 with work at the time of diagnosis
* Presenting a unilateral breast cancer exclusively local extension
* Having received surgery
* Reporting of adjuvant chemotherapy (+ / - trastuzumab)
* Reporting to radiotherapy or not (If radiotherapy, it will be done on site investigator)
* In work at the time of diagnosis (employees, traders and professionals)
* Patient affiliated to a social security scheme
* Consent signed by the patient before the implementation of any specific procedure to study
Exclusion Criteria:
* Presence of in situ lesions, cancer recurrence, metastatic disease immediately, location bilateral
* Inability physical, psychological, psychiatric or cognitive responses to the questionnaires and participate in interviews
* Recognition previous ALD (due to another disease)
* Patient under guardianship
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Comparison of the effect of early individualized psychosocial assets versus a standard support on social inequalities in the rate of return to work