Clinical trial · Observational
Evolution of Body Connection After Surgery
Evolution of Body Connection and Identity Post-surgery: The Pancreas Cancer Case
NCT04422730CI-TRIAL-00091142completedClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Evaluation of psychological impact of patients after pancreatectomy because of cancer diagnosis. Patients will be evaluated with questionnaires after and before intervention. 3 control groups will be used to compare de psychological impact.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Pancreas Cancer | Pancreatic Carcinoma | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Psychological evaluation | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (4)
- label
- pancreatectomy in cancer patients
- interventionNames
- Behavioral: Psychological evaluation
- label
- pancreatectomy in non-cancer patients
- interventionNames
- Behavioral: Psychological evaluation
- label
- mastectomy
- interventionNames
- Behavioral: Psychological evaluation
- label
- Acute leukaemia
- interventionNames
- Behavioral: Psychological evaluation
Primary outcomes (5)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Patient is older than 18 years old * With a good understanding and practice of the French language * And depending on the group, experimental or control, presenting: * pancreatic cancer expected to be treated with pancreatectomy or planned to be treated with pancreatectomy excluding cancer or breast cancer scheduled to be treated with mastectomy or acute leukaemia at a recent diagnosis (21 days). * No patient's opposition to the information provided * Affiliated to the social security plan or beneficiary Exclusion Criteria: * Other medical or psychiatric condition, * Level of cognitive efficiency incompatible with response to questions about himself, * A person in an emergency situation, a person under legal protection or unable to express the non opposition to their participation to research.
References
Publications (0)
Data not yet available
No reference posted for this study.