RETAIN: Retaining Opioid Users Entering Medication Assisted Treatment and Encouraging HCV/HIV Testing (RETAIN)
Retaining Opioid Users Entering Medication Assisted Treatment and Encouraging HCV/HIV Testing Through Active Patients Sharing Experiences and the Provision of Information About Infections -an electroNic-health Application
The purpose of this research study is to:
- assess how well individuals entering medication assisted treatment like the RETAIN e-health application as measured by their feedback on the intervention.
- test the impact of RETAIN on knowledge about medication-assisted treatment(MAT).
- assess treatment retention rates in patients completing the RETAIN intervention.
- test the impact of RETAIN on knowledge about HCV/HIV
- test the impact of RETAIN on interest in being tested for HCV/HIV
調査の概要
詳細な説明
The pre-post study of RETAIN will: 1) assess the acceptability of RETAIN as measured by participant feedback about the intervention; 2) test the impact of RETAIN on knowledge about MAT, as measured by the MAT Knowledge Assessment; 3) assess MAT retention rates in patients completing the RETAIN intervention; 4) test the impact of RETAIN on knowledge about HCV/ HIV; 5) test the impact of RETAIN on interest in being tested for HCV/HIV.
The acceptability of RETAIN will be assessed with a feedback form which includes questions about how helpful the intervention was (scale of 1-4), what the patient liked most and least about the intervention, and any suggestions for improving it. The average (and standard deviation) for the rated helpfulness of the intervention will be derived and the qualitative data about what they liked most and least about the intervention and suggestions for improvement will be tabulated. Pre-/post-changes in the percent of correct knowledge assessment items (i.e., about MAT and HCV/HIV) and interest in HCV/HIV testing will be analyzed using a Wilcoxon signed-rank test. The 3- and 6-month retention rates for RETAIN participants will be compared, using Fisher's exact tests, to the overall treatment retention rates at 3- and 6- months for the UC Health MAT clinics as determined by the retrospective chart review.
研究の種類
入学 (実際)
段階
- 適用できない
連絡先と場所
研究場所
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Ohio
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Cincinnati、Ohio、アメリカ、45229
- University of Cincinnati Addiction Sciences Division
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参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
Inclusion Criteria:
- At least 18 years of age
Starting MAT with methadone or suboxone or in MAT for less than 2 weeks;
Exclusion Criteria:
- Does not sign the "short form" consent form
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
- 主な目的:防止
- 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 |
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実験的:RETAIN
Participants who meet criteria will receive the RETAIN self-administered, e-health application intervention.
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RETAIN is a self-administered, e-health application and includes short videos in which patients who are successfully engaged in MAT discuss what they wish they had known about MAT and its benefits when they started treatment.
The intervention is designed to maximize "scalability" - the administration would entail handing an electronic device (e.g., tablet, laptop, etc.) to an individual who would then self-administer the intervention.
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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 |
---|---|---|
treatment retention status after 3 months
時間枠:3 months
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To compare with retention rates for the overall MAT clinics and use in sample size calculations for potential follow-on trial
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3 months
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
---|---|---|
treatment retention status after 6 months
時間枠:6 months
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To compare with retention rates for the overall MAT clinics and use in sample size
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6 months
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MAT Knowledge Assessment
時間枠:Pre and Post Tests in E-Health App Day 1
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To test the impact of RETAIN on knowledge about MAT
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Pre and Post Tests in E-Health App Day 1
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The Injection-Related Infection and Treatment Survey (I-RITS)
時間枠:Pre and Post Tests in E-Health App Day 1
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To test the impact of RETAIN on knowledge about HCV and HIV
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Pre and Post Tests in E-Health App Day 1
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Feedback on the RETAIN e-health application
時間枠:Day 1
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feedback includes questions about how helpful the intervention was (scale of 1-4), what the patient liked most and least about the intervention, and any suggestions for improving it.
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Day 1
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協力者と研究者
スポンサー
研究記録日
主要日程の研究
研究開始 (実際)
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 (実際)
学習記録の更新
投稿された最後の更新 (実際)
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。
self-administered, e-health applicationの臨床試験
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American University of Beirut Medical Center完了
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The Hong Kong Polytechnic UniversityTung Wah College; Hospital Authority, Hong Kong募集
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University of PennsylvaniaFox Chase Cancer Center完了
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LMU KlinikumPreventicus GmbH; Versicherungskammer Bayern積極的、募集していない
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University Health Network, Toronto募集
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University of California, San FranciscoPatient-Centered Outcomes Research Institute完了
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Universiti Teknologi MaraMinistry of Education, Malaysiaまだ募集していませんメタボリック・シンドローム