Hysterectomy Clinical Trials

Clinical trials related to Hysterectomy Procedure

Effect of Reading a Personal Narrative Book on Emotional Regulation in Women of Childbearing Age Undergoing Hysterectomy: A Randomized Controlled Trial (RELIEF)

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goal of this interventional clinical trial involving minimal risks and constraints is to evaluate whether an innovative approach to managing catastrophizing in the preoperative context of hysterectomy improves psychological outcomes compared to usual care in women of childbearing age who have been informed of an indication for hysterectomy. The main questions it aims to answer are: * Does the use of a personal narrative book improve adaptive emotional regulation and reduce catastrophizing, anxiety, and depressive symptoms in the preoperative period? * Does this intervention improve postoperative patient satisfaction and reduce the need for additional supportive measures? Researchers will compare standard care (CNGOF information leaflet with psychological consultation if needed) with an intervention including a personal narrative book in addition to standard care, to see if the intervention improves emotional regulation, psychological well-being, and satisfaction. Participants will: * provide explicit oral informed consent; * complete questionnaires on their emotional and psychological experience; * read a personal narrative book if they are randomized to the intervention group.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Maximum Age: 42
Healthy Volunteers: f
View:

• Women aged 18 years or older and under 43 years of age

• Patients with an indication for hysterectomy for a non-malignant condition

• Patients who have provided explicit oral consent to participate

• Patients covered by the French social security system

• Patients able to read and understand French and capable of reading a French book within a timeframe compatible with the study schedule

Locations
Other Locations
France
Clinique Tivoli-Ducos
RECRUITING
Bordeaux
Time Frame
Start Date: 2026-05-13
Estimated Completion Date: 2028-01
Participants
Target number of participants: 156
Treatments
No_intervention: Standard care
CNGOF information leaflet with a consultation with a psychologist or other additional supportive measures if needed.
Experimental: Intervention (Personal Narrative arm)
CNGOF information leaflet, personal narrative book, and a consultation with a psychologist or other additional supportive measures if needed.
Related Therapeutic Areas
Sponsors
Leads: Groupe SantéCité SantéCité Enseignement-Recherche-Innovation (GCS SCERI)

This content was sourced from clinicaltrials.gov