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临床试验/NCT02919917
NCT02919917已完成2 期

Treatment of Post-SCI Hypotension: A Randomized Controlled Study of Usual Care Versus Anti Hypotension Therapy

James J. Peters Veterans Affairs Medical Center2 个研究点 分布在 1 个国家目标入组 66 人开始时间: 2017年6月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
66
试验地点
2
主要终点
Affected Therapy Sessions

研究概览

简要总结

While treatment strategies for OH have been identified for use in persons with acute SCI, the field of SCI medicine lacks a gold standard for treatment thresholds and well-defined outcome parameters. Comprehensively documenting the impact of orthostatic hypotension (OH), regardless of symptoms, during acute rehabilitation and identifying the effects of two different treatment approaches on therapy participation and adherence to an intended rehabilitation plan could have a significant impact on clinical practice in the acute rehabilitation setting following SCI.

详细描述

Baseline Testing: Subjects will visit the testing laboratory on the SCI Rehabilitation Unit for baseline data collection, prior to initiation of the treatment protocol. Upon arrival, subjects will be placed in the supine position on an adjustable surface for instrumentation, which will be conducted in a quiet, dimly lit, thermo-neutral testing environment. After a 20-minute period of quiet rest, a 10-minute sample of supine heart rate (HR), respiratory rate, BP and CBF velocity data will be collected. Venous occlusion plethysmography (Vop) will be collected in the supine position for two 5-minute periods. After the supine data collection, subjects will be passively moved into the seated position, with the knees and hips at 90°, for the 10-minute seated data collection period. Subjects will be asked to complete two surveys related to AD and OH symptomology. Finally, subjects will be fitted with a 24-hour HR and BP monitor and will be asked to go about their normal routine. A record of all daily activities including rehabilitation, medications, eating and sleep/wake times will be logged. This testing session should take approximately 1 hour.

Daily Testing: Every day supine and seated BP measurements will be performed at least three times per day. These BP assessments will be recorded in the supine and seated positions in the subject's room by a patient care associate who is blind to the study arm allocation. For every scheduled physical and occupational therapy session, the treating therapist will be asked to complete a brief 6 question survey to document if that session was altered, disrupted, or missed due to hypotension (Therapist Reported Version). The subject will also be asked to complete a brief survey to determine if from their perspective the session was altered, disrupted or missed due to hypotension (Subject Reported Version). In addition, every day a co-investigator and the attending physician for that subject will complete an EMR review of queried BP values within the previous 24 hours, symptoms of low BP, adverse events related to high or low BP, and will review (and act upon for the usual care arm) the protocol treatment decision tree.

Weekly Testing: At weekly intervals of between 6 and 8 days, subjects will be asked to visit the testing laboratory on the SCI Rehabilitation Unit. Procedures for the weekly testing sessions will be the same as for the Baseline Testing. The 24-hour BP assessment will be conducted twice weekly.

Discharge Testing: At discharge subjects will undergo similar testing as described during the Baseline and Weekly Testing with the addition of the Patient Global Impression of Change survey, which will be administered by the Mount Sinai Site Research Assistant.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Care Provider)

盲法说明

Therapists administering rehabilitation will be blinded to the randomization of patients enrolled in the study.

入排标准

年龄范围
18 Years 至 89 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Any level of injury;
  • Any AIS grade of SCI;
  • Non-ventilator dependent
  • Primarily wheelchair dependent for mobility;
  • Duration of injury < 1 year
  • Systolic BP less than 110 mmHg and/or diastolic BP less than 70 mmHg for males.
  • Systolic BP less than 100 mmHg and/or diastolic BP less than 70 mmHg for females
  • Primary Language is English.
  • Able to provide informed consent

排除标准

  • Have insufficient mental capacity to independently provide informed consent
  • Have insufficient English speaking or reading ability to provide informed consent or complete assessments in English
  • Have contraindications to the use of midodrine hydrochloride
  • Are pregnant

研究组 & 干预措施

Usual Care Group

Experimental

Individuals randomized to the usual care group will receive BP management according to the usual care in current practice in the SCI Rehabilitation Unit.

Will receive treatment only if they experience symptoms that are associated with low BP (dizziness, lightheadedness, nausea, blurry vision, loss of consciousness, etc.).

Treatment to lessen or eliminate these symptoms of low blood pressure will be guided by the attending physician and can include physical countermeasures to increase blood pressure (abdominal binders, comperssion stockings, etc.) and/or midodrine .

干预措施: Midodrine Hydrochloride (Drug)

BP Threshold Treatment Group

Experimental

Individuals assigned to the BP threshold treatment group will receive BP management, regardless of symptoms, to maintain systolic BP between 111-135 mmHg for males and 101-135 mmHg for females for the duration of their in-patient hospital stay.

This treatment will be started based on your low BP, regardless of if you experience symptoms that are associated with low BP (dizziness, lightheadedness, nausea, blurry vision, loss of consciousness, etc.). Before you start on any medication you will receive physical countermeasures to increase blood pressure (abdominal binders, comperssion stockings, etc.).

If your blood pressure remains low after using these countermeasures you will begin to take midodrine 3 times a day as described in the intervention section. The dosage will increase and be stopped once until your seated SBP is between 111-135 mmHg.

干预措施: Midodrine Hydrochloride (Drug)

结局指标

主要结局

Affected Therapy Sessions

时间窗: Inpatient hospitalization (up to 4 months)

Responses to the questions "was the therapy session affected by low BP or concern for low BP development?" between the usual care and BP threshold treatment groups. The percent of sessions with a "yes" response are reported.

Systolic Blood Pressure

时间窗: Inpatient hospitalization (up to 4 months)

Systolic hypertension (\>/= 140 mmHg)

次要结局

  • Systolic Blood Pressure(Inpatient Hospitalizations (up to 4 months))
  • Missed Therapy Sessions(Inpatient Hospitalizations (up to 4 months))

研究者

发起方
James J. Peters Veterans Affairs Medical Center
申办方类型
Fed
责任方
Principal Investigator
主要研究者

Jill M. Wecht, Ed.D.

Principal Invesitgator

James J. Peters Veterans Affairs Medical Center

研究点 (2)

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