Decision Support Workshop for Breast Reconstruction (DSW)

This study is currently recruiting participants. (see Contacts and Locations)
Verified May 2013 by University Health Network, Toronto
Sponsor:
Collaborator:
The Physicians' Services Incorporated Foundation
Information provided by (Responsible Party):
University Health Network, Toronto
ClinicalTrials.gov Identifier:
NCT01857882
First received: May 6, 2013
Last updated: May 15, 2013
Last verified: May 2013
  Purpose

The purpose of this study is to determine the effectiveness of a pre-consultation decision support workshop for breast reconstruction after breast cancer, in facilitating the decision-making process, compared to routine pre-surgical education.


Condition Intervention
Breast Cancer
Other: Decision Support Workshop

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Supportive Care
Official Title: Breast Reconstruction Decision Workshop Pilot RCT (Randomized Controlled Trial)

Resource links provided by NLM:


Further study details as provided by University Health Network, Toronto:

Primary Outcome Measures:
  • Decision self-efficacy [ Time Frame: Change from baseline decision self-efficacy at 1 week after surgical consultation ] [ Designated as safety issue: No ]
    Decision self-efficacy (DSE) scale is a prospectively designed instrument to evaluate patient self-confidence in decision-making, including shared decision-making. It has been validated among women facing treatment decisions for osteoporosis and used in cancer patients. Psychometric evaluation has shown high levels of internal consistency (Cronbach alpha 0.90). Decision self-efficacy is correlated with decision conflict subscales of feeling informed (r = 0.47) and supported (r = 0.45). This instrument has never been tested in the breast cancer or breast reconstruction population.


Secondary Outcome Measures:
  • Decision Conflict [ Time Frame: Change from baseline decision conflict at 1 week after surgical consultation ] [ Designated as safety issue: No ]
    Decision conflict scale measures personal perceptions of uncertainty in choosing options and has been demonstrated to be valid and responsive to change. The decisional conflict scale is a 16-item 5-response instrument that reports a score from 0 - 100 with higher scores indicating more conflict (items are summed, divided by 16 and multiplied by 25).

  • Decision Preference and Decision Choice [ Time Frame: baseline ] [ Designated as safety issue: No ]
    Decision Preference and Decision Choice has been used as a primary and secondary outcome in studies of decision support interventions in cancer patients. It demonstrates good test-retest reliability (test-retest coefficient > 0.90) and is sensitive to change when measured before and after an intervention.

  • Patient involvement in care scale (PICS) [ Time Frame: T1 (1 week after surgical consultation) ] [ Designated as safety issue: No ]
    PICS is a measure of patient perception of involvement with her care, and has seven 5-point Likert scale items that assess the extent to which the patient asked questions, offered opinions, and expressed concerns when meeting with the surgeon.

  • Satisfaction with Information (sub-scale of BREAST-Q) [ Time Frame: T1 (1 week after surgical consultation) ] [ Designated as safety issue: No ]
    The BREAST-Q is a procedure-specific and validated PRO that measures Hr-QOL and patient satisfaction with breast reconstruction. The "Satisfaction with Information" Subscale specifically measures patient satisfaction with the preoperative information and care provided by the plastic surgeon and other members of the medical team. There are 15 items that use a four-level Likert scale response format, the score is transformed on a scale of 0 to 100 with higher scores indicating greater satisfaction.

  • Qualitative interview assessment [ Time Frame: Within three months after initial consultation ] [ Designated as safety issue: No ]
    A subgroup of participants allocated to both the experimental and usual care groups will be asked to participate in a brief qualitative telephone interview. Purposeful sampling will be used to recruit 5 patients from each group to achieve data saturation and variability. Telephone interviews will be conducted by a social worker trained in qualitative methods. All participants randomized to the workshop will additionally be asked to complete a written survey for evaluation of the intervention immediately after participation in the workshop.

  • Uptake rate of breast reconstruction-Service outcome [ Time Frame: Six months after initial consultation ] [ Designated as safety issue: No ]
    The uptake rate of breast reconstruction (if patients chose breast reconstruction or no reconstruction)

  • Length of consultation-service outcome [ Time Frame: Duration of initial consultation ] [ Designated as safety issue: No ]
    The length of the initial consultation with the plastic surgeon, measured in minutes. Consultations are expected to be between 20-60 mins.

  • Number of consultations-service outcomes [ Time Frame: Six months after initial consultation ] [ Designated as safety issue: No ]
    The number of consultations with the plastic surgeon until the patient has made a reconstruction choice (defined as signing a surgical consent form) will be recorded. Patients can spend months considering their choices, so it is appropriate to follow them for a period of at least six months after their initial consultation.

  • Breast reconstruction knowledge test [ Time Frame: Change in baseline breast reconstruction knowledge at 1 week after initial consultation ] [ Designated as safety issue: No ]
    This breast reconstruction knowledge test is a 12-item 3-response questionnaire that records the score on a continuous integer scale, and measured patient's knowledge regarding breast reconstruction.

  • Spielberger State-Trait Anxiety Inventory (STAI) [ Time Frame: Change from baseline anxiety at 1 week after initial consultation ] [ Designated as safety issue: No ]
    STAI is a 20-item measure of anxiety and its scores using the state version of the Spielberger State Trait Anxiety Scale (20 items) and its scores range from 20-80, with a higher score indicating greater anxiety. Trait will only be measured at baseline, while the change from baseline state anxiety to 1 week after initial consultation will be measured.

  • Medical Outcomes Study Social Support Survey [ Time Frame: baseline ] [ Designated as safety issue: No ]
    Medical Outcomes Study Social Support Survey has a series of 18 questions that measure 4 domains of social support (emotional, tangible, affectionate, and social interactions). Responses range from 1 (none of the time) to 5 (all the time). The items in each domain were summed and then transformed to yield scores ranging from 0 to 100. Higher scores indicate more support.


Other Outcome Measures:
  • Recruitment rate-feasibility outcome [ Time Frame: Duration of recruiting, expected on average two months ] [ Designated as safety issue: No ]
    As this is a pilot study, the feasibility of conducting the study is highly important. The recruitment rate of participants will be measured, during the recruiting period which is expected to be on average two months.

  • Retention after randomized treatment assignment (workshop and consultation attendance)-feasibility outcome [ Time Frame: Duration of treatment-8 hours on day of treatment ] [ Designated as safety issue: No ]
    The number of participants who completed their assigned treatment (workshop and consultation vs. consultation alone) will be recorded. This will be recorded directly after each day the treatment is delivered.

  • Completion of primary outcome measure-feasibility outcome [ Time Frame: 1 week after initial consultation ] [ Designated as safety issue: No ]
    Patients are to complete the primary outcome one week after initial consultation. However, it is expected that some patients may take longer to complete this intervention (on average 1 month after consultation), and will require reminder telephone calls.


Estimated Enrollment: 40
Study Start Date: September 2012
Estimated Study Completion Date: September 2013
Estimated Primary Completion Date: July 2013 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Decision Support Workshop
The decision support workshop will be 2 hours in duration on the morning of the consultation and will be facilitated by a dedicated social worker from psycho-oncology.
Other: Decision Support Workshop

Incorporates the key components of shared decision-making and decision support with the philosophy of delivering supportive care to cancer patients.

  • Surgeon (30 mins): treatment options for breast reconstruction with indications/ contraindications, advantages / disadvantages, expected post-operative course, aesthetic result and complications with probabilities
  • Registered nurse (30 mins): preparing for surgery, postoperative recovery and how to navigate the health care system
  • Social worker (30 mins): values clarification exercise
  • Breast reconstruction patient volunteer (30 mins) questions and answers about her personal experience
No Intervention: Standard Care
Routine pre-consultation education

Detailed Description:

Postmastectomy breast reconstruction is becoming increasingly utilized in breast cancer patients to provide surgical restoration of the breast mounds. The breast reconstruction discussions can be highly complex, as there are many different techniques, timing, and complications that are unique to each procedure. However ¼ of women report being dissatisfied with some component of their cancer or reconstructive care. Failure of the physician to provide adequate information about treatment options is the most frequent source of cancer patient dissatisfaction and breast reconstruction patients have expressed a need for further information regarding the complex decision to pursue breast reconstruction. In such scenarios of complex medical decision-making, decision support techniques may be an effective solution to information provision and shared decision-making. As a result, the investigators developed a pre-consultation educational group intervention delivered in a group setting for women considering breast reconstruction, with the aims to fill an existing information-gap, promote high-quality decision-making and enhance decision self-efficacy and other decision measures. This pilot study will be the first step in the evaluation of the educational group intervention and the results will be used to determine the feasibility and inform the optimal design for a definitive randomized controlled trial. This study will first examine the feasibility and acceptability of the intervention through implementation in a pilot, mixed-methods, 1:1 allocation parallel-arm randomized controlled trial.

  Eligibility

Ages Eligible for Study:   18 Years to 79 Years
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Patient age: 18 - 79 years at the time of consultation
  • In situ or invasive biopsy confirmed breast adenocarcinoma
  • Considered for immediate or delayed breast reconstruction
  • First consultation for breast reconstruction

Exclusion Criteria:

  • Chest wall or atypical breast malignancy (ex: angiosarcoma) or inflammatory adenocarcinoma of the breast
  • Completion any phase of reconstruction, or for revision reconstruction
  • Patient cannot read or write in English.
  • Cognitive impairment or uncontrolled psychiatric diagnosis
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01857882

Contacts
Contact: Toni Zhong, MD, MHS 416-340-3858 toni.zhong@uhn.on.ca
Contact: Natalie Causarano, MSc 416-340-4800 ext 6598 natalie.causarano@uhn.ca

Locations
Canada, Ontario
Toronto General Hospital Recruiting
Toronto, Ontario, Canada, M5G 2C4
Contact: Toni Zhong, MD, MHS    416-340-3858    toni.zhong@uhn.ca   
Contact: Natalie Causarano, MSc    416-340-4800 ext 6598    natalie.causarano@uhn.ca   
Principal Investigator: Toni Zhong, MD, MHS         
Sub-Investigator: Jennica Platt, MD         
Sub-Investigator: Jennifer Jones, PhD         
Sponsors and Collaborators
University Health Network, Toronto
The Physicians' Services Incorporated Foundation
Investigators
Principal Investigator: Toni Zhong, MD, MHS University Health Network, Toronto
  More Information

No publications provided by University Health Network, Toronto

Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: University Health Network, Toronto
ClinicalTrials.gov Identifier: NCT01857882     History of Changes
Other Study ID Numbers: 11-1027-CE
Study First Received: May 6, 2013
Last Updated: May 15, 2013
Health Authority: Canada: Ethics Review Committee

Keywords provided by University Health Network, Toronto:
breast cancer
breast reconstruction
shared decision making
decision support intervention

Additional relevant MeSH terms:
Breast Neoplasms
Neoplasms by Site
Neoplasms
Breast Diseases
Skin Diseases

ClinicalTrials.gov processed this record on August 20, 2014