A Study of Survivorship Service Capacities Among Health Care Agencies in New York City
To describe the range of services available to cancer survivors in the NYC area.
To determine organizations' need for assistance to enhance services for survivors.
調査の概要
状態
条件
詳細な説明
To describe the range of services available to cancer survivors in the NYC area.
To determine organizations' need for assistance to enhance services for survivors.
研究の種類
連絡先と場所
研究場所
-
-
New York
-
New York、New York、アメリカ、10065
- Memorial Sloan-Kettering Cancer Center
-
-
参加基準
適格基準
就学可能な年齢
- 子
- 大人
- 高齢者
健康ボランティアの受け入れ
受講資格のある性別
サンプリング方法
調査対象母集団
説明
Inclusion Criteria:
To be eligible to participate in the study, an agency must:
Be a current provider of either:
- General health services (GHS), such as primary care, health education and wellness, mental health services, home health care, palliative care, or cancer screening and diagnosis;
- Cancer-specific medical treatments (CMT), such as cancer surgery, radiation, chemotherapy, hormonal therapy; experimental therapies; cancer pain and symptom management; rehabilitation services; post-treatment monitoring and surveillance; or prophylactic treatments, such as chemoprevention; or
- Any type of specialized 'post-cancer' or 'after-cancer' medical care or support services (SMC) (i.e., psychotherapeutic, relationship and family, psycho-educational,wellness and quality of life)
- Be located within the five boroughs of New York City
- Have been serving cancer patients for 12 months or longer, and
- Be willing and able to identify an English-speaking representative, 21 years of age or older as its designated key informant.
Exclusion Criteria:
- We will limit this study to provider agencies such as hospitals, diagnostic centers, clinics, health and human service agencies, and grassroots community organizations and public service settings that offer programs for cancer survivors. Independent practitioners or private practice settings will not be surveyed. Our survey questions are intended for major health services organizations and are not appropriate for private practices settings.
We will use our screening questionnaire to determine where or not a given agency should be included or excluded from the study AGENCY SCREENER.
研究計画
研究はどのように設計されていますか?
デザインの詳細
コホートと介入
グループ/コホート |
介入・治療 |
---|---|
1
Data about participating agencies will be collected by electronic survey.
Agencies will be identified using the NYSDOH's existing mailing list of care facilities located in the five boroughs of New York City, referral databases and resource guides created by the American Cancer Society (ACS), the New York Hospital Directory.
|
A cancer care facility or 'agency' is the study's unit of analysis.
Data about participating agencies will be collected by electronic survey.
Agencies will be identified using the NYSDOH's existing mailing list of care facilities located in the five boroughs of New York City, referral databases and resource guides created by the American Cancer Society (ACS), the New York Hospital Directory
|
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 |
時間枠 |
---|---|
To determine agencies' need for assistance to enhance services for survivors.
時間枠:2 years
|
2 years
|
協力者と研究者
捜査官
- 主任研究者:David Loundsbury, PhD、Memorial Sloan Kettering Cancer Center
出版物と役立つリンク
研究記録日
主要日程の研究
研究開始
一次修了 (実際)
研究の完了 (実際)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (見積もり)
学習記録の更新
投稿された最後の更新 (見積もり)
QC基準を満たした最後の更新が送信されました
最終確認日
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。
すべてのがんの臨床試験
-
Syracuse UniversityBill and Melinda Gates Foundation; Texas A&M University; Jimma University完了
-
Ottawa Hospital Research Instituteまだ募集していません
-
Institut National de la Santé Et de la Recherche...完了