WE-CARE Community Health Forums to Increase Breast Cancer Screening and Clinical Trial Participation for Rural and Low Income Women
2026年9月10日 更新者：Mayo Clinic
A Community Engagement Approach to Increasing Breast Cancer Screening and Clinical Trial Participation in Low Income and Rural Populations ('WE-CARE')
This clinical trial tests how well the Women's Engagement for Cancer Awareness, Resources, and Education (WE-CARE) community health forums work to increase breast cancer screening and clinical trial participation for rural and low income women.
Despite advances in breast cancer diagnosis and treatment in the past decade, rural-dwelling and underserved women, and Black, Indigenous, and people of color continue to experience low rates of breast cancer screening.
Since the survival rate for breast cancer is largely dependent on stage at which it is diagnosed, later stage breast cancer is correlated to a poorer prognosis and higher mortality rate.
The WE-CARE community health forms address structural barriers through culturally tailored educational sessions on breast cancer risk, screening and clinical trials, survivor storytelling to humanize cancer and research and patient navigation to facilitate mammogram screening and address barriers.
The WE-CARE community health forums may be an effective way to increase breast cancer screening and clinical trial participation for rural and low income women.
調査の概要
研究の種類
介入
入学 (実際)
1
段階
- 適用できない
連絡先と場所
このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。
研究場所
-
-
Wisconsin
-
Eau Claire、Wisconsin、アメリカ、54701
- Mayo Clinic Health System-Eau Claire Clinic
-
-
参加基準
研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
いいえ
説明
Inclusion Criteria:
- Female
- Be between the ages of 50 and 74 years
- Have no prior history of breast cancer screening (i.e., who have either never received a mammogram or have not had one in the past five years)
- Reside in a rural community in Wisconsin or belong to low income (self-reported)
- Be able to speak and understand English or Spanish
- Be willing and able to provide informed consent
Exclusion Criteria:
- Women who have received a mammogram within the past five years
- Have a current or prior diagnosis of breast cancer
- Are currently undergoing treatment for any active malignancy
- Have cognitive or psychiatric impairments that, in the judgment of the study team, would preclude meaningful participation
研究計画
このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。
研究はどのように設計されていますか？
デザインの詳細
- 主な目的：ヘルスサービス研究
- 割り当て：なし
- 介入モデル：単一グループの割り当て
- マスキング：なし（オープンラベル）
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的：Health services research (WE-CARE forum)
Patients attend a WE-CARE community forum, over 2 hours.
At the forum, patients attend educational sessions on breast cancer risk, screening and clinical trials as well as survivor storytelling sessions by community companions who have participated in clinical research for breast cancer.
Patients also receive navigation support to facilitate mammography, address barriers, support scheduling, coordinate follow-up, and provide real-time guidance on screening and matching with clinical trials or registries.
|
Attend education sessions at WE-CARE forum
他の名前：
Receive navigation support
他の名前：
Attend storytelling sessions at WE-CARE forum
他の名前：
|
この研究は何を測定していますか？
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Recruitment yield
時間枠：At time of forum
|
Assessed via the number enrolled divided by the number of eligible participants approached.
|
At time of forum
|
|
Exposure reach (community level reach)
時間枠：At time of forum
|
Assessed by the number of attendees divided by the estimated number of population indirectly exposed (e.g., via flyers, social media, community announcements).
|
At time of forum
|
|
Retention
時間枠：From baseline to 3 months
|
Assessed by the number of participants who complete 3-month follow-up.
|
From baseline to 3 months
|
|
Perceived participant satisfaction
時間枠：Immediately following completion of forum
|
Success is defined as ≥ 75% of participants rating the experience ≥ 4 on a 5-point scale rated on a 5-point scale where 1=strongly disagree and 5=strongly agree.
Higher scores indicate greater perceived satisfaction.
|
Immediately following completion of forum
|
|
Perceived barriers to engagement and community impact
時間枠：Immediately following completion of forum
|
Assessed by post-intervention focus groups and brief qualitative interviews.
Results will be analyzed descriptively.
|
Immediately following completion of forum
|
|
Perceived facilitators to engagement and community impact
時間枠：Immediately following completion of forum
|
Assessed by post-intervention focus groups and brief qualitative interviews.
Results will be analyzed descriptively.
|
Immediately following completion of forum
|
|
Perceived acceptability - AIM
時間枠：Immediately following completion of forum
|
Assessed using the Acceptability of Intervention Measure (AIM), which consists of 4 items (e.g., meets my approval, is appealing to me) each rated on a 5-point scale where 1=strongly disagree and 5=strongly agree.
Higher scores indicate greater perceived acceptability.
|
Immediately following completion of forum
|
|
Perceived appropriateness - IAM
時間枠：Immediately following completion of forum
|
Assessed using the Intervention Appropriateness Measure (IAM), which consists of 4 items (e.g., seems fitting, seems like a good match) each rated on a 5-point scale where 1=strongly disagree and 5=strongly agree.
|
Immediately following completion of forum
|
|
Perceived feasibility - FIM
時間枠：Immediately following completion of forum
|
Assessed using the Feasibility of Intervention Measure (FIM), which consists of 4 items (e.g., seems implementable, seems easy to use) each rated on a 5-point scale where 1=strongly disagree and 5=strongly agree.
Higher scores indicate greater perceived acceptability.
|
Immediately following completion of forum
|
その他の成果指標
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Change in breast cancer screening intention
時間枠：Baseline, 3-month follow-up, 6-month follow-up
|
Assessed using the Risk Behavior Diagnosis Scale (RBDS), which consists of 12 items each rated on a 7-point scale where 1=strongly disagree and 7=strongly agree.
Higher scores reflect greater intention to engage in screening behavior.
|
Baseline, 3-month follow-up, 6-month follow-up
|
|
Chang in breast cancer screening behavior
時間枠：At 6 months post-forum
|
For participants who have never had a mammogram, a follow-up question at six months post-forum will document self-reported mammography completion.
Verification will be optional and used only to evaluate feasibility of data collection.
Results will be analyzed descriptively.
|
At 6 months post-forum
|
|
Perceived trust in medical researchers
時間枠：Baseline, 3-month follow-up, 6-month follow-up
|
Will be assessed using the Trust in Medical Researchers Scale, which consists of 4 items each rated on a 5-point scale where 1=strongly disagree and 5=strongly agree.
higher scores indicating greater perceived trust.
Results will be analyzed descriptively.
|
Baseline, 3-month follow-up, 6-month follow-up
|
|
Change in perceived research readiness
時間枠：Baseline, 3-month follow-up, 6-month follow-up
|
Indicators of research interest will be assessed using descriptively based on subsequent participant enrollment in observational research.
|
Baseline, 3-month follow-up, 6-month follow-up
|
協力者と研究者
ここでは、この調査に関係する人々や組織を見つけることができます。
スポンサー
捜査官
- 主任研究者：Pravesh Sharma, MD、Mayo Clinic Health System-Eau Claire Clinic
出版物と役立つリンク
研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。
便利なリンク
研究記録日
これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。
主要日程の研究
研究開始 (実際)
2026年6月30日
一次修了 (実際)
2026年9月10日
研究の完了 (実際)
2026年9月10日
試験登録日
最初に提出
2026年6月3日
QC基準を満たした最初の提出物
2026年6月8日
最初の投稿 (実際)
2026年6月12日
学習記録の更新
投稿された最後の更新 (実際)
2026年9月14日
QC基準を満たした最後の更新が送信されました
2026年9月10日
最終確認日
2026年9月1日
詳しくは
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。