The Impact of Home Delivery of Antiretroviral Therapy on Virological Suppression
2018年3月2日 更新者:Till Barnighausen、Harvard School of Public Health (HSPH)
The Impact of Home Delivery of Antiretroviral Therapy on Virological Suppression: A Non-inferiority Cluster-randomized Controlled Trial in Dar es Salaam, Tanzania
Home delivery of antiretroviral therapy (ART) by community health workers (CHWs) has the potential to reduce key barriers to ART care retention.
The aim of this study is to determine whether CHW-led home delivery of ART for patients who are stable on ART combined with facility-based care for those not stable on ART is non-inferior to the standard of care (facility-based care for all ART patients) in achieving and maintaining virological suppression.
The primary endpoint of this trial is the proportion of ART patients (regardless of whether they were clinically stable on ART at enrollment) who are in viral failure at the end of the study period.
The non-inferiority design applies only to this primary endpoint.
The margin of non-inferiority was set at a Risk Ratio (comparing intervention to control) of 1.45.
This is a cluster-randomized controlled trial set in Dar es Salaam.
The unit of randomization is a healthcare facility with its surrounding neighborhoods (the 'catchment area').
We matched all 48 healthcare facilities offering ART services and having affiliated public-sector CHWs in Dar es Salaam into pairs (stratified by district) based on having a similar number of patients currently on ART.
In each pair, one cluster was randomized to the intervention and one to the control arm.
The intervention consists of home visits by CHWs to provide counseling and deliver ART to patients who are stable on ART, while the control is the standard of care (facility-based ART care and CHW home visits at least every three months without ART home delivery).
In addition, within each study arm, half of the healthcare facilities were randomized to enhanced CHW-led nutrition counseling and half to standard counseling.
調査の概要
研究の種類
介入
入学 (実際)
2172
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
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Dar es Salaam、タンザニア
- Management and Development for Health
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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
18年歳以上 (大人、高齢者)
健康ボランティアの受け入れ
いいえ
受講資格のある性別
全て
説明
Inclusion Criteria:
- Having attended one of the participating healthcare facilities for ART care during the enrolment period
- Living in a neighborhood that is in the healthcare facility's catchment area
Exclusion Criteria:
- ART patients who are pregnant at the time of enrollment
- Inability to provide written informed consent
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:ランダム化
- 介入モデル:階乗代入
- 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:ART home delivery + enhanced nutrition counseling
Community health workers visit participants at home (maintaining patients' prior clinic visit frequency) to deliver antiretroviral therapy (ART) and to provide standard plus enhanced nutrition counseling.
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Community health workers visit participants who are clinically stable on antiretroviral therapy (ART) at home (maintaining patients' prior clinic visit frequency) to deliver ART.
Clinically stable on ART was defined as 1) taking ART for at least six months, 2) having had a CD4-cell count >350 cells/μL or a suppressed viral load at six or more months after ART initiation, and 3) the patient's most current CD4-cell count must have been >350 cells/μL or the most current viral load must have shown viral suppression, with the last measurement not taken more than 12 months ago.
Community health workers visit participants at home to provide standard counseling (focusing on family planning, prevention of HIV transmission, and ART adherence) plus enhanced nutrition counseling (covering food production and dietary advice).
In addition, participants who state that they have access to a plot of land or garden to grow vegetables receive a pack of seeds (amaranth, cowpea, or pumpkin) at enrolment.
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実験的:ART home delivery + no enhanced nutrition counseling
Community health workers visit participants at home (maintaining patients' prior clinic visit frequency) to deliver antiretroviral therapy (ART) and to provide standard counseling.
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Community health workers visit participants who are clinically stable on antiretroviral therapy (ART) at home (maintaining patients' prior clinic visit frequency) to deliver ART.
Clinically stable on ART was defined as 1) taking ART for at least six months, 2) having had a CD4-cell count >350 cells/μL or a suppressed viral load at six or more months after ART initiation, and 3) the patient's most current CD4-cell count must have been >350 cells/μL or the most current viral load must have shown viral suppression, with the last measurement not taken more than 12 months ago.
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実験的:No ART home delivery + enhanced nutrition counseling
Community health workers visit participants at home to provide enhanced nutrition counseling.
Participants will not receive ART home delivery.
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Community health workers visit participants at home to provide standard counseling (focusing on family planning, prevention of HIV transmission, and ART adherence) plus enhanced nutrition counseling (covering food production and dietary advice).
In addition, participants who state that they have access to a plot of land or garden to grow vegetables receive a pack of seeds (amaranth, cowpea, or pumpkin) at enrolment.
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介入なし:Standard of care
Participants in this arm receive facility-based ART care and no enhanced nutrition counseling.
They receive community health worker visits as per the standard of care in Dar es Salaam.
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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 |
時間枠 |
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The proportion of participants in viral failure, comparing participants that received the intervention (ART home delivery if stable on ART or standard facility-based care if unstable) versus those that received the standard of care.
時間枠:At the end of the study period
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At the end of the study period
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The mean BMI of participants in clusters assigned to standard counseling by CHWs versus those in clusters assigned to standard plus enhanced nutrition counseling.
時間枠:At the end of the study period
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At the end of the study period
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二次結果の測定
結果測定 |
時間枠 |
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Participants' healthcare expenditures
時間枠:In the last six months
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In the last six months
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Self-reported ART adherence
時間枠:In the last one month
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In the last one month
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The proportion of patients with access to a plot of land who grow vegetables or fruits for their own consumption.
時間枠:At the end of the study period
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At the end of the study period
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Diversity of dietary intake
時間枠:At the end of the study period
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At the end of the study period
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The proportion of patients who are anemic
時間枠:At the end of the study period
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At the end of the study period
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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。
捜査官
- 主任研究者:Till Bärnighausen, MD ScD、Harvard School of Public Health (HSPH)
- 主任研究者:Pascal Geldsetzer, MBChB MPH、Harvard School of Public Health (HSPH)
- 主任研究者:Nzovu Ulenga, MD、Management and Development for Health
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。
一般刊行物
- Geldsetzer P, Francis JM, Sando D, Asmus G, Lema IA, Mboggo E, Koda H, Lwezaula S, Ambikapathi R, Fawzi W, Ulenga N, Barnighausen T. Community delivery of antiretroviral drugs: A non-inferiority cluster-randomized pragmatic trial in Dar es Salaam, Tanzania. PLoS Med. 2018 Sep 19;15(9):e1002659. doi: 10.1371/journal.pmed.1002659. eCollection 2018 Sep.
- Geldsetzer P, Francis JM, Ulenga N, Sando D, Lema IA, Mboggo E, Vaikath M, Koda H, Lwezaula S, Hu J, Noor RA, Olofin I, Larson E, Fawzi W, Barnighausen T. The impact of community health worker-led home delivery of antiretroviral therapy on virological suppression: a non-inferiority cluster-randomized health systems trial in Dar es Salaam, Tanzania. BMC Health Serv Res. 2017 Feb 22;17(1):160. doi: 10.1186/s12913-017-2032-7.
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)
2016年3月1日
一次修了 (実際)
2018年2月1日
研究の完了 (実際)
2018年2月1日
試験登録日
最初に提出
2016年3月12日
QC基準を満たした最初の提出物
2016年3月16日
最初の投稿 (見積もり)
2016年3月17日
学習記録の更新
投稿された最後の更新 (実際)
2018年3月6日
QC基準を満たした最後の更新が送信されました
2018年3月2日
最終確認日
2018年3月1日
詳しくは
本研究に関する用語
その他の研究ID番号
- RIDIE-STUDY-ID-562a718b12fa0
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米国FDA規制医薬品の研究
いいえ
米国FDA規制機器製品の研究
いいえ
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