University of Virginia Health System
Charlottesville, Virginia, 22908, United States
NCT Number: NCT07653087
This research study is testing a decision aid to help patients think through whether to have sentinel lymph node biopsy for melanoma.
Sentinel lymph node biopsy (SLNB) can be a difficult decision for some patients because the potential benefits and risks may not be clear. This study is being done to learn whether providing structured, easy-to-understand information helps patients feel more informed and less uncertain about their decision.
Patients in this study will be given a paper decision aid (DA). Patients will be given other short questionnaires to complete before and after the decision aid.
Trial opening soon.
Get Notified18 year and older
All sexes
Interventional
Not applicable
Charlottesville, Virginia, 22908, United States
The melanoma-specific decision aid (DA) is a structured, evidence-based informational tool designed to support shared decision-making regarding sentinel lymph node biopsy (SLNB). The DA includes: (1) a plain-language explanation of melanoma staging and the purpose of SLNB; (2) individualized estimates of SLNB positivity risk based on the MIA risk model; (3) a balanced presentation of the potential benefits, risks, and uncertainties associated with SLNB; and (4) a values clarification component prompting patients to reflect on personal preferences related to risk tolerance, diagnostic certainty, and potential downstream treatment implications. The decision aid is provided to patients prior to surgical consultation and is reviewed during the clinic visit to facilitate structured discussion between the patient and surgeon. The decision aid does not provide treatment recommendations and does not replace physician counseling.
Immediately after written informed consent and before reviewing the decision aid, patients will complete baseline questionnaires reflecting their understanding and feelings following standard-of-care counseling alone. These baseline measures include:
After reviewing the decision aid and participating in a brief follow-up discussion with the clinician, patients will complete post-decision aid questionnaires, including:
A 30-day chart review will document whether SLNB was ultimately performed.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The melanoma-specific decision aid is a structured, evidence-based informational tool designed to support shared decision-making regarding sentinel lymph node biopsy. The DA is a paper based tool that includes: (1) a plain-language explanation of melanoma staging and the purpose of SLNB; (2) individualized estimates of SLNB positivity risk based on the MIA risk model; (3) a balanced presentation of the potential benefits, risks, and uncertainties associated with SLNB; and (4) a values clarification component prompting patients to reflect on personal preferences related to risk tolerance, diagnostic certainty, and potential downstream treatment implications. The decision aid is provided to patients prior to surgical consultation and is reviewed during the clinic visit to facilitate structured discussion between the patient and surgeon. The decision aid does not provide treatment recommendations and does not replace physician counseling.
Time frame: From the time of enrollment to the end of the intervention on Day 1
Change in decisional conflict score from pre-decision aid to post-decision aid, measured using a validated questionnaire (Decisional Conflict Scale - DCS).
Time frame: From the time of enrollment to the end of the intervention on Day 1
Change in patient knowledge regarding sentinel lymph node biopsy.
Time frame: From the time of enrollment to the end of the intervention on Day 1
Change in consultation-related anxiety using the STAI-6 validated questionnaire
Time frame: 30 days post-clinic visit
The proportion of patient participants who elect to undergo sentinel lymph node biopsy after decision aid-supported consultation
Time frame: Within 48 hours of the intervention on Day 1
The Decision Aid Evaluation Form will be used to describe patient-reported acceptability of the decision aid. This questionnaire utilizes Likert-scale items and an optional, written, free-text response section.
Time frame: From the time of enrollment to the end of the intervention on Day 1
Proportion of eligible patients successfully completing review of the decision aid during the clinic visit
Contact information is provided by the study sponsor or research team.
University of Virginia
Other
Acronym: Mel73
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT06900582
Endometrial Cancer, Endometrial Neoplasms
View Trial DetailsNCT07146295
Breast Cancer, Breast Diseases
Alkmaar, Netherlands
View Trial DetailsNCT07278726
ALND, Sentinel Lymph Node Biopsy (SLNB)
Bologna, Italy
View Trial DetailsNCT07085442
Axilla; Breast, Axillary Lymph Nodes Dissection
Burnley, United Kingdom
View Trial Details