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Self Directed Stations for the Stroke Patient

2019年6月5日 更新者:Baylor Research Institute
Early initiation of therapy post stroke has been associated with improved long-term outcomes, and functional activity dose during the first week of inpatient rehabilitation predicts both gait velocity at discharge and length of time to independent walking. The primary study objective is to pilot the feasibility of integrating a patient-directed activity program into inpatient rehabilitation following stroke. The second study objective is to identify if participation in the patient-directed activity program improves functional ability and health related quality of life.

調査の概要

状態

完了

条件

詳細な説明

1 BACKGROUND AND RATIONALE

1.1 Background

Due to the high incidence of stroke, increased risk of developing secondary (e.g., pain, depression, urinary tract infections, pressure ulcers, falls, and seizures) and chronic conditions (e.g., second stroke, CVD), high medical costs 1, evolving healthcare system (e.g., reimbursement, length of stay, staffing productivity 2, healthcare professionals are challenged to explore and develop innovative strategies to continue to achieve the best clinical practice and outcomes for patients. Functional activity levels are typically low during inpatient rehabilitation post stroke 3-6, emphasized by King and colleagues 7 who reported that patients post stroke undergoing inpatient rehabilitation spent 76% of their day in their bedroom and 62% being inactive. Consequently, since dose of functional activity (amount of active time and/or quantity of repetitions) is posited to relate to outcomes 8-11, the optimal conditions for inpatient rehabilitation are being questioned. The literature is clear that low functional activity reflects low potential for neuroplasticity. Consequently, novel and feasible methods to provide higher doses of functional activity during inpatient rehabilitation, that realistically considers cost-effectiveness and resource allocation 12, are important to improve functional outcomes post stroke 13.

1.2 Rationale for Protocol

Early initiation of therapy post stroke has been associated with improved long-term outcomes 14, and functional activity dose (e.g., activity time, number of repetitions) during the first week of inpatient rehabilitation predicts both gait velocity at discharge and length of time to independent walking 15. Specifically, patients who completed more than the median number of exercise repetitions (703) during the first week of inpatient rehabilitation experienced quicker recovery of unassisted walking 15. This lack of activity is a significant issue during inpatient rehabilitation and for overall recovery as repetitive task practice is argued to drive neural plasticity following stroke 16,17. Specifically, there is a growing body of evidence indicating that increased functional activity and large volume of practice during inpatient rehabilitation is required to induce improved stretch reflex modulation and increased neuromuscular activation 11, thus leading to meaningful neural adaptations and recovery following stroke 16. However, our current clinical practice of 3-hours of therapy during inpatient rehabilitation (which is standard of care for inpatient rehabilitation hospitals) may not be adequate to facilitate neuroplasticity and achieve optimal functional outcomes 10. This is emphasized by the fact that Medicare beneficiaries with stroke undergoing inpatient rehabilitation experienced shorter LOS, had worsening admission and discharge function, and had fewer community discharges 18. Therefore, our objective in this proposal is to evaluate the feasibility and effectiveness of implementing a novel intervention to facilitate patient-directed activity for individuals undergoing inpatient rehabilitation. The goal of the intervention is to increase repetition, stimulation, attention, and therapeutic activity of the affected extremities and trunk to facilitate improved outcomes following stroke 17,19,20. This will be achieved by adding up to 1.5-hours of daily patient-directed activities into the individuals schedule beyond the 3-hours of therapy provided by clinicians, thus increasing daily therapeutic activity time by up to 50%. The activities will include physical (PT) and occupational therapy (OT) tasks (see table 1 below for more details). The activities are therapeutic in nature, include typical activities that patients would complete during the 3-hours of therapy provided as standard of care, are low intensity, and include activities that involve being seated or prone on a gym mat.

It is important to note that the clinical team at Baylor Institute for Rehabilitation has been implementing up to 1.5-hours of additional daily therapy into standard of care since January 2014. However, to date we have not collected any effectiveness data so the clinical and research team wanted to demonstrate through a research project that the addition of the extra 1.5-hours of daily therapy is beneficial beyond the 3-hours of therapy currently provided as standard of care. Since starting the additional therapy in January 2014 the clinical team has had 25 patients successfully move through rehabilitation and no patients have had any adverse events.

2.1 Primary Objectives

Pilot the feasibility of integrating the novel patient-directed activity program into inpatient rehabilitation following stroke. Based on guidelines for conducting an a priori pilot study we will assess aspects of the process (e.g., eligibility, randomization), resources (e.g., equipment, space), management (e.g., staff capacity for data entry and management), and scientific basis (e.g., sensitive outcome measures) of the intervention. Our working hypothesis is that that the patient-directed activity program will be successfully integrated into patient and clinical schedule.

2.2 Secondary Objectives

To identify if participation in the novel patient-directed activity program improves functional ability and health related quality of life (HRQOL) in patients post stroke. Our working hypothesis is that patients' post stroke that actively participate in the program will manifest significant increases in functional ability and HRQOL at discharge to inpatient rehabilitation and at the follow-up appointment within 6 months of discharge when compared to controls.

3 INVESTIGATIONAL PLAN

3.1 Study Design

We will use a randomized controlled trial and include stroke patients who are undergoing inpatient rehabilitation at Baylor Institute for Rehabilitation (BIR). Participants will be randomized into an experimental (patient-directed station program) or control group (standard of care).

研究の種類

介入

入学 (実際)

73

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

    • Texas
      • Dallas、Texas、アメリカ、75246
        • Baylor Research Institute

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:

  • 18 years of age and older
  • Safe to be left unsupervised as deemed by therapist or has caregiver present
  • Diagnosed with stroke in past six months
  • Medically stable as deemed by therapy team
  • >3 on FIM comprehension
  • Primary diagnosis of stroke (all types)

Exclusion Criteria:

  • Pre-morbid developmental disability
  • Significant pre-morbid psychological diagnosis or concurrent TBI
  • Other cognitive impairment that would prevent participation as determined by the clinician

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:単一グループの割り当て
  • 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
実験的:Patient Directed Exercise Group
Participants will complete a combination of PT and OT activities that will be individually prescribed based on an evaluation by the therapy team completed pre-intervention. The activities will be added to the comprehensive inpatient rehabilitation program.
Combination of PT and OT activities that will be individually prescribed based on an evaluation by the therapy team completed pre-intervention. The activities will be added to the comprehensive inpatient rehabilitation program.
介入なし:Standard of care
Standard of care comprehensive inpatient rehabilitation program.

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
Pittsburgh Rehabilitation Participation Scale
時間枠:Daily during inpatient rehab hospitalization, time frame maximum is up to 3 months
Daily measurements will be recorded during inpatient hospitalization to capture changes in participation between admission and discharge and to calculate sums/averages of participation.
Daily during inpatient rehab hospitalization, time frame maximum is up to 3 months

二次結果の測定

結果測定
メジャーの説明
時間枠
Stroke Rehabilitation Assessment of Movement Measure (STREAM)
時間枠:Wtihin one week of rehab inpatient admission, within one week of rehab inpatient discharge, at post discharge follow up (3-6 months after inpatient rehab discharge)
Wtihin one week of rehab inpatient admission, within one week of rehab inpatient discharge, at post discharge follow up (3-6 months after inpatient rehab discharge)
WOLF Motor Function Test
時間枠:Wtihin one week of rehab inpatient admission, within one week of rehab inpatient discharge, at post discharge follow up (3-6 months after inpatient rehab discharge)
Wtihin one week of rehab inpatient admission, within one week of rehab inpatient discharge, at post discharge follow up (3-6 months after inpatient rehab discharge)
Actigraph
時間枠:Wtihin one week of rehab inpatient admission, within one week of rehab inpatient discharge
Wtihin one week of rehab inpatient admission, within one week of rehab inpatient discharge
Functional Independence Measure
時間枠:Wtihin one week of rehab inpatient admission, within one week of rehab inpatient discharge, at post discharge follow up (3-6 months after inpatient rehab discharge)
Wtihin one week of rehab inpatient admission, within one week of rehab inpatient discharge, at post discharge follow up (3-6 months after inpatient rehab discharge)
Stroke Impact Scale
時間枠:Within one week of rehab inpatient discharge, at post discharge follow up (3-6 months after inpatient rehab discharge)
Within one week of rehab inpatient discharge, at post discharge follow up (3-6 months after inpatient rehab discharge)
Patient Participation Survey
時間枠:Within one week of rehab inpatient discharge
Within one week of rehab inpatient discharge
Therapist Feasibility Survey
時間枠:After patient accrual, up to 12 months
After all patients have been accrued, a one-time feasibility survey will be distributed to treating therapists to assess feasibility with implementing extra physical activity with stroke patients.
After patient accrual, up to 12 months

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。

スポンサー

捜査官

  • 主任研究者:Molly Trammell, PT、Physical Therapist

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)

2014年10月1日

一次修了 (実際)

2019年4月1日

研究の完了 (実際)

2019年6月1日

試験登録日

最初に提出

2015年2月19日

QC基準を満たした最初の提出物

2015年5月13日

最初の投稿 (見積もり)

2015年5月18日

学習記録の更新

投稿された最後の更新 (実際)

2019年6月7日

QC基準を満たした最後の更新が送信されました

2019年6月5日

最終確認日

2019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

  • 014-203

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