Preventing Amputations by Tailored Risk-based Intervention to Optimize Therapy (PATRIOT)
調査の概要
詳細な説明
Amputation is a devastating complication of diabetes that is preceded in > 80% of cases by foot ulcers. Veterans with diabetes are at risk for incident foot ulcers, particularly if they have neuropathy, vascular disease or anatomic abnormalities. This risk is worsened if they have poor foot self-care, poor foot self-monitoring and/or poor control of A1c and other risk factors. It is important to activate at-risk Veterans to improve self-care and self-monitoring, and lower other amputation risks.
The PATRIOT study is a randomized controlled trial (RCT) testing the effectiveness of a personalized behavioral intervention (PBI) aimed to improve foot self-care, foot self-monitoring, and modifiable risks for amputation such as A1c, BP, LDL and smoking using behavioral counseling combined with dermal thermometry. The primary specific aim is to evaluate the effect of PBI on the proportion of foot lesions (ulcerative or non-ulcerative) compared to current best practice (CBP) care for diabetes. The secondary specific aims are to evaluate the impact of PBI on foot self-care skills, foot education and adherence, A1c, BP and LDL, and quality of life at 6 months as well as its longer-term effects at 12 months; and cost-effectiveness compared to CBP. The will also examine the effect of PBI and CBP on demonstrated foot self-care, plantar pressures, inflammation, satisfaction and intervention acceptability.
The investigators will randomize 404 adults with diabetes who are at higher than normal risk of foot ulcers [Risk score of 1, 2 or 3 (with no history of ulcers or amputations)] to the PBI and CBP equally. The PBI is a cohesive, personalized intervention targeting foot self-care and self-monitoring that includes dermal thermometry, diet, exercise, and medication-taking incorporating self-regulatory theory, the Transtheoretical Model and Prospect Theory and delivered using Motivational Interviewing principles and the teach back method. The interventions will be standardized and fidelity of the intervention will be maintained. Through a blinded RCT, the investigators will test the effect of PBI in relation to CBP. Key outcomes are non-ulcerative and ulcerative lesions, foot-care skills, foot care education, adherence to diet and medication, general and foot health-specific quality of life, A1c, BP, and LDL. Outcomes will be measured at baseline, 6 and 12 months. All analyses will be intent-to-treat.
This study will evaluate a cohesive risk-stratified personalized behavioral intervention aimed to improve self-care, enhance self-monitoring and reduce incident ulcers in adults without a previous diabetic foot ulcer. This study applies established behavioral theories combined with new technology to intervene and improve care for adults with diabetes who are at risk for amputation. If this promising theory-driven primary prevention approach to prevent foot lesions can work in a clinical setting where improvements in foot care are urgently needed, it will be an important scientific contribution that could lower the risk of amputation in adults with diabetes.
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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New York
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New York、New York、アメリカ、10010
- Manhattan Campus of the VA NY Harbor Healthcare System, New York, NY
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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:
- Adults with diabetes and PAVE score 1, 2 or 3, drug therapy for > 6 months
- An available phone
- At least 2 primary care visits in the previous 1.5 years at the recruitment site
Exclusion Criteria:
- Patients with acute CVD events < 3 months ago
- 86 poor estimated short-term survival (< 1 year)
- Recent major surgery (< 3 months)
- Inability to exercise
- Prior toe or foot amputation
- Prior foot ulcer
- Temporary residence in the area
- Inability to provide consent will be excluded
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:ランダム化
- 介入モデル:並列代入
- マスキング:ダブル
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:Personalized Behavioral Intervention (PBI)
The PBI is a 12-month long integrated, multicomponent counseling and dermal thermometry intervention targeting foot self-care, foot self-monitoring, diet, medication and physical activity.
The intervention is based on self-regulation theory, the Transtheoretical Model and
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The PBI is based on self-regulation theory, the Transtheoretical Model and Prospect Theory, and will be delivered using Motivational Interviewing principles and the teach-back method.
Participants will receive monthly calls targeting foot self-care, foot self-monitoring, diet, medication and physical activity for 6 months.
Call/mailing frequency during the next 6 months will depend on adherence level to foot self-care and self-monitoring at 6 months.
他の名前:
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プラセボコンパレーター:Current Best Practice (CBP)
This group will receive all the enhancements that the VA has targeted to improve foot risk in diabetes and foot care, and will also receive counseling regarding preventing general health conditions.
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CBP will include monthly calls from a counselor focusing on preventing conditions like colorectal cancer, flu, insomnia, vision problems, memory loss and oral disease for the first 6 months.
Frequency of calls and mailings from counselors during the next 6 months will be determined by level of adherence to preventive strategies during the first 6 months.
他の名前:
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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 |
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Ulcerative and non-ulcerative Foot lesions
時間枠:12 months
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High-resolution standard view digital photographs of the feet and footwear will be obtained and reviewed by the investigators blinded to group assignment, and a suspected ulcer or nonulcerative plantar lesion below the malleoli will be referred to a blinded (as to group assignment) adjudicators, all clinical experts.
Lesions will be judged as absent/nonulcerative lesion/ulcer
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12 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 |
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Foot care skills
時間枠:12 months
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The investigators will use the Veterans foot self-care education and behavior survey to assess foot care.
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12 months
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Foot-care education
時間枠:12 months
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The investigators will use the Veterans foot self-care education and behavior survey to assess basic foot-care education and extended foot-care education.
This survey was developed and validated in high-risk Veterans.
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12 months
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Medication adherence
時間枠:12 months
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This will be assessed primarily by refill frequency using the pharmacy database , supplemented by the self-reported medication-taking scale.
Refill compliance is an objective measurement of medication adherence that utilizes pharmacy records to assess the proportion of time a patient has medication available.
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12 months
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Diet
時間枠:12 months
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Diet will be assessed by food frequency questionnaire
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12 months
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Physical activity
時間枠:12 months
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Physical activity will be assessed via accelerometer.
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12 months
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A1c
時間枠:12 months
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Fasting blood will be processed for A1c.
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12 months
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Systolic blood pressure
時間枠:12 months
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Blood pressure will be measured with an Omron automated machine and the mean of 6 BP's over 2 hours.
used.
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12 months
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LDL
時間枠:12 months
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Fasting blood will be processed for LDL cholesterol.
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12 months
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Health-related quality of life
時間枠:12 months
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General health-related quality of life will be assessed using the Veterans SF-12.
The investigators will also measure foot health-specific quality of life.
Measures are reliable and valid.
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12 months
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Cost-effectiveness
時間枠:12 months
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The investigators will measure direct medical costs (costs of drugs, tests, supplies, personnel, and facilities),direct non-medical costs (transportation), and indirect (patient's time and caregiver's time).
The investigators will also calculate quality-adjusted life years using the ED-5D survey to adjust for health states.
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12 months
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協力者と研究者
捜査官
- 主任研究者:Sundar Natarajan, MD MSc、Manhattan Campus of the VA NY Harbor Healthcare System, New York, NY
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 (見積もり)
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。
Personalized Behavioral Interventionの臨床試験
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University of MichiganNational Institute on Drug Abuse (NIDA)完了
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University of Southern CaliforniaNational Institutes of Health (NIH)積極的、募集していない
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