- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT03105076
Impact of Decision Aids on Breast Cancer Surgery Choice: A Randomized Controlled Trial
Studieoversigt
Detaljeret beskrivelse
Background:
For women with early-stage breast cancer, both simple mastectomy and breast conservation therapy (BCT) with radiotherapy yield similar survival rates, making psychological adjustment and quality-of-life issues pivotal in treatment choice. Using decision aids (DAs) is one way to provide information to patients and to involve them in making decisions about their treatment. We have developed a DAs to be administered after consultation for Taiwanese women deciding on breast surgery, and plan to conduct a randomized controlled trial (RCT) to evaluate the benefit of DAs on breast surgery decision making.
Patients and Methods:
Decision aids are interventions designed to help patients with early breast cancer to make deliberate choices among treatment options by providing information on those options and any potential outcome relevant to different breast cancer surgeries. Women considering breast cancer surgery are randomly assigned to receive a DAs or the standard oral conversation (control condition) after initial consultation, wherein surgeons disclosed the diagnosis and discussed treatment options with patients. Participants complete interview-based questionnaires 1 day before and 4 weeks after surgery. Primary outcome measures 1 day before surgery are decisional conflict and decision-making difficulties after consultation. Secondary outcomes are decision regret and postsurgical depression 1 month after surgery.
Hypothesis:
The DAs group are predicted to lower decisional conflict scores before surgery, and lower decision regret scores and depression scores 1 month after surgery compared with women in the control arm. Our study hopes to support the efficacy of DAs in helping breast cancer women to arrive at their breast surgery decision.
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
-
-
-
New Taipei City, Taiwan
- Shuang Ho Hospital, Taipei Medical University
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- Taiwanese women newly diagnosed with stage 0 to 3 breast cancer (including patients with ductal carcinoma in situ), who were suitable for breast surgery
- Patients who were able to give consent and complete the interview
Exclusion Criteria:
- Patients were diagnosed with nonmalignant breast disease
- Patients were offered neoadjuvant chemotherapy
- Patients had cognitive impairment
- Patients were physically unfit to be interviewed
- Patients were non-Mandarin or -Taiwanese
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Sundhedstjenesteforskning
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Dobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
---|---|
Eksperimentel: DAs gruppe
Fælles beslutningstagning ved hjælp af beslutningshjælpemidler
|
Fælles beslutningstagning med beslutningshjælpemidler
|
Ingen indgriben: Kontrolgruppe
Standard mundtlig forklaring guidet med hæfter
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
Decisional conflict
Tidsramme: 1 day before surgery
|
Total score of decisional conflict scale
|
1 day before surgery
|
Knowledge
Tidsramme: 1 day before surgery
|
Total score on knowledge scale
|
1 day before surgery
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
Decision regret
Tidsramme: 4 weeks after surgery
|
Total score of decision regret
|
4 weeks after surgery
|
Postsurgical depression
Tidsramme: 4 weeks after surgery
|
Total score of Hospital anxiety and depression scale (HADS)
|
4 weeks after surgery
|
Samarbejdspartnere og efterforskere
Efterforskere
- Ledende efterforsker: Shared Decision Making Resource Center, Shuang Ho Hospital, Taipei Medical University
Publikationer og nyttige links
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- W105HHC-07
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
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