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Incentives for Primary Care Use in a Safety Net Setting

2018年6月11日 更新者:Virginia Commonwealth University

Incentives for Primary Care Use: A Randomized Controlled Trial in a Safety Net Setting

A randomized controlled trial (RCT) of incentives for an initial primary care visit within 6 months of enrollment in a health care coverage program. Study subjects are drawn from a low-income adult population that gains coverage and access to community-based primary care services under a program administered by an academic safety-net hospital. The investigators will offer financial incentives to encourage an initial primary care visit within 6 months of enrollment and evaluate whether the primary care visit altered subsequent health seeking behavior and influenced patient satisfaction and other outcomes such as self-reported health status.

調査の概要

詳細な説明

A randomized controlled trial (RCT) of incentives for an initial primary care visit within 6 months of enrollment in a health care coverage program. Study subjects are drawn from a low-income adult population that gains coverage and access to community-based primary care services under a program administered by an academic safety-net hospital. The investigators will offer financial incentives to encourage an initial primary care visit within 6 months of enrollment and evaluate whether the primary care visit altered subsequent health seeking behavior and influenced patient satisfaction and other outcomes such as self-reported health status.

Incentives should steer patients in their decision to seek primary care, reduce barriers to care, and ultimately improve patient health and reduce utilization and costs through their relationship with a PCP. This study is the first of its kind to incentivize low-income patients. This population has the greatest need for health care and exerts the greatest pressure on the United States' safety net system. Furthermore, the safety net population is the target of policies such as Medicaid eligibility expansions, yet urban safety net patients are largely understudied. These patients are rarely given the opportunity to participate in research, and when they are the subjects of measures to reduce health care utilization, they are the subject of policies using negative incentives such as those that introduce cost sharing for using ED services.1 Alternatively, safety net providers invest in case management systems to reduce utilization. The proposed study is a departure from prior measures to reduce utilization among low-income patients by focusing on patients and using positive incentives. The study borrows from the principles of behavioral economics to motivate patients towards primary care utilization. Once in the primary care system, The investigators will test whether primary care contact reduces more expensive forms (e.g., inpatient, ED) of health care.

The investigators will compare outcomes of patients assigned in the highest incentive group ($50) to patients assigned to the modest incentive group ($25) and to patients assigned to usual care (no incentive, but assignment to a PCP). The investigators will also compare incentive patients ($50, $25) to a contemporaneous group of patients that enroll in the safety net clinic at the same time.

研究の種類

介入

入学 (実際)

1228

段階

  • 適用できない

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

21年~64年 (大人)

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:

  • Adults between ages 21-64 years
  • No prior enrollment in VCC for the past 12 months
  • English or Spanish speaking, and
  • Can be contacted by mail and telephone (preferably) or willing to be interviewed in person.

Exclusion Criteria:

  • Unable to be contacted by phone/mail
  • Cannot provide consent
  • No longer located in catchment area

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:並列代入
  • マスキング:独身

武器と介入

参加者グループ / アーム
介入・治療
介入なし:Contemporaneous Control
This group is our 'usual care' control group. They were not contacted for an interview and were not offered an incentive to visit their primary care physician.
アクティブコンパレータ:$0 group
This group completed a baseline interview but was not offered any incentive if they visited their primary care physician.
Those assigned to the $0 group will not receive an incentive for visiting their PCP.
実験的:$25 group
This group completed a baseline interview and was offered $25 they visited their primary care physician within 6 months.
Those assigned to the $25 group will receive $25 if they visit their PCP within 6 months of study enrollment.
実験的:$50 group
This group completed a baseline interview and was offered $50 they visited their primary care physician within 6 months.
Those assigned to the $50 group will receive $50 if they visit their PCP within 6 months of study enrollment.

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
The number of Primary Care Physician visits will be assessed using medical claims record data.
時間枠:This will be assessed in the 6 months following study enrollment.
The number of primary care visits to a primary care physician will be collected from medical claims record data.
This will be assessed in the 6 months following study enrollment.

二次結果の測定

結果測定
メジャーの説明
時間枠
The time to a Primary Care Physician will be assessed using medical claims record data.
時間枠:This will be assessed in the 6 months following study enrollment.
The time to a primary care visits to a primary care physician will be collected from dates available in the medical claims record data.
This will be assessed in the 6 months following study enrollment.

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:Cathy Bradley, Phd、PI

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

2014年1月1日

一次修了 (実際)

2016年11月8日

研究の完了 (実際)

2016年11月8日

試験登録日

最初に提出

2016年9月28日

QC基準を満たした最初の提出物

2016年10月3日

最初の投稿 (見積もり)

2016年10月4日

学習記録の更新

投稿された最後の更新 (実際)

2018年6月12日

QC基準を満たした最後の更新が送信されました

2018年6月11日

最終確認日

2018年6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

  • HM20000002
  • 1R01HS022534 (米国 AHRQ グラント/契約)

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

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。

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