Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04177628
Other study ID # DBCG RT SDM
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 4, 2020
Est. completion date July 31, 2023

Study information

Verified date October 2023
Source Vejle Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this project is to elucidate whether the use of shared decision making will influence patient engagement in the decision making process about adjuvant radiotherapy after breast conserving surgery for local breast cancer or early stages of local breast cancer.


Description:

The risk of recurrence of breast cancer is lowered by adjuvant medical treatment as well as by radiotherapy (RT). On the other hand, all adjuvant treatments involve a risk of side effects; some are acute and transient while others are long-term. Considering the well-known side effects of irradiation, it seems appropriate to involve patients in the decision on whether to receive irradiation. In the shared decision making (SDM) process clinicians and patients work together to make appropriate health decisions based on clinical evidence and the patient's informed preferences. A patient decision aid (PtDA) is instrumental in the SDM process. This study is a multicenter, national trial randomizing doctors to either use or not use SDM and a PtDA when informing the patients about benefits and risks of receiving adjuvant radiotherapy. It is not expected that significantly less patients will receive radiotherapy as a consequence of SDM. The primary aim of the study is to evaluate whether patient engagement in decision making is affected by SDM and the use of an in-consultation PtDA.


Recruitment information / eligibility

Status Completed
Enrollment 678
Est. completion date July 31, 2023
Est. primary completion date December 31, 2022
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - Histologically verified breast cancer or ductal carcinoma in situ breast cancer - Candidate for adjuvant radiotherapy Danish Breast Cancer Group type F after breast-conserving surgery for T1-2, N0-Nmi, M0 disease according to national guidelines. - Signed confirmation of participation. Exclusion Criteria: - Bilateral breast cancer or suspicion of disseminated cancer - Unable to understand the information, the planned treatment or follow-up for any reason. - Earlier radiotherapy towards the thoracic region.

Study Design


Intervention

Behavioral:
Shared decision making supported by an in-consultation patient decision aid
After having received training in SDM, the doctor will practice SDM supported by an in-consultation PtDA during the consultation with the participant.

Locations

Country Name City State
Denmark Aalborg Hospital Aalborg
Denmark Aarhus University Hospital Aarhus
Denmark Rigshospitalet Copenhagen
Denmark Herlev University Hospital Herlev
Denmark Sjaellands University Hospital Næstved
Denmark Odense University Hospital Odense
Denmark Vejle Hospital Vejle

Sponsors (4)

Lead Sponsor Collaborator
Vejle Hospital Danish Breast Cancer Cooperative Group, Danish Comprehensive Cancer Center, University of Southern Denmark

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Participant engagement in the decision making process as measured by the Shared Decision Making Questionnaire 9. Minimum value: 0. Maximum value: 100. The higher the value the more patient engagement. Within one week after the consultation
Secondary The doctor's perception of patient engagement in the decision making process as measured by the Shared Decision Making Questionnaire doctor 9 Minimum value: 0. Maximum value: 100. The higher the value the more patient engagement. Within one week after the consultation
Secondary The participant's fear of cancer recurrence as measured by the Fear of Cancer Recurrence Short form Questionnaire Minimum value: 0. Maximum value: 36. The higher the value the more fear of recurrence. Within one week after the consultation and again after six months
Secondary The participant's engagement in the decision making process as measured by the Shared Decision Making Process 4 questionnaire Minimum score: 0. Maximum score: 4. The higher the score the more patient engagement. Within one week after the consultation
Secondary The participant's effectiveness in decision making as measured by the Decisional Conflict Scale questionnaire Minimum value: 0. Maximum value: 100. The higher the value the more effective decision making. Before (12 items) and within one week after the consultation (all 16 items)
Secondary The participant's regret of the treatment decision as measured by the Decision Regret Scale questionnaire Minimum value: 0. Maximum value: 100. The higher the value the more regret. Six months after the consultation
Secondary The participant's engagement in the decision making process as measured by the CollaboRATE questionnaire Minimum score: 0. Maximum score: 9. The higher the value the more patient engagement. Within one week after the consultation
Secondary The participant's quality of life as measured by the EORCT QLQ-C30 (version 3.0) questionnaire, only question 29 + 30 Minimum value: 0. Maximum value: 100. The higher the value the more quality of life. Six months
See also
  Status Clinical Trial Phase
Enrolling by invitation NCT05558917 - Comparison Between PECS BLOCK 2 vs ESP BLOCK in Ocnologic Breast Surgery N/A
Active, not recruiting NCT03664778 - Abbreviated Breast MRI After Cancer Treatment
Recruiting NCT03144622 - 18F-FSPG PET/CT Imaging in Patients With Cancers
Completed NCT05452499 - Pain Neuroscience Education and Therapeutic Exercise as a Treatment for Breast Cancer Survivors Living With Sequelae N/A
Active, not recruiting NCT04568902 - Study of H3B-6545 in Japanese Women With Estrogen Receptor (ER)-Positive, Human Epidermal Growth Factor Receptor 2 (HER2)-Negative Breast Cancer Phase 1
Completed NCT02860585 - Evaluation of Survival in Patients With Metastatic Breast Cancer Receiving High-dose Chemotherapy With Autologous Haematopoietic Stem Cell Transplantation N/A
Completed NCT04059809 - Photobiomodulation for Breast Cancer Radiodermatitis Phase 2/Phase 3
Recruiting NCT04557449 - Study to Test the Safety and Tolerability of PF-07220060 in Participants With Advance Solid Tumors Phase 1/Phase 2
Completed NCT03698942 - Delphinus SoftVueâ„¢ ROC Reader Study
Completed NCT00092950 - Exercise in Women at Risk for Breast Cancer Phase 2
Terminated NCT04123704 - Sitravatinib in Metastatic Breast Cancer Phase 2
Not yet recruiting NCT02151071 - The Breast Surgery EnLight and LightPath Imaging System Study Phase 1/Phase 2
Recruiting NCT02934360 - TR(ACE) Assay Clinical Specimen Study N/A
Active, not recruiting NCT02950064 - A Study to Determine the Safety of BTP-114 for Treatment in Patients With Advanced Solid Tumors With BRCA Mutations Phase 1
Not yet recruiting NCT02876848 - A Novel E-Health Approach in Optimizing Treatment for Seniors (OPTIMUM Study) N/A
Completed NCT02931552 - Nuevo Amanecer II: Translating a Stress Management Program for Latinas N/A
Recruiting NCT02547545 - Breast Cancer Chemotherapy Risk Prediction Mathematical Model N/A
Completed NCT02652975 - Anticancer Treatment of Breast Cancer Related to Cardiotoxicity and Dysfunctional Endothelium N/A
Completed NCT02518477 - Preventive Intervention Against Lymphedema After Breast Cancer Surgery N/A
Completed NCT02303366 - Pilot Study of Stereotactic Ablation for Oligometastatic Breast Neoplasia in Combination With the Anti-PD-1 Antibody MK-3475 Phase 1