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The Effect of Early Mobilization in Mild to Moderate Hemorrhagic Stroke

Primary Purpose

Hemorrhagic Stroke

Status
Completed
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
early mobilization
early standard intervention
Sponsored by
National Taiwan University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hemorrhagic Stroke focused on measuring Early mobilization, Acute stroke, Early intervention, Early mobilization therapy

Eligibility Criteria

20 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

The inclusion criteria will be as follows:

  1. patients with a first time intracerebral (either cortical or subcortical) hemorrhage with unilateral hemiparesis/ hemiplegia confirmed by magnetic resonance imaging or computed tomography;
  2. patients with no contraindications to being mobilized (early intervention) within 24 hours of stroke onset (based on the medical team's clinical judgment: including systolic blood pressure (SBP)<160mmHg in resting; resting heart rate (HR)<130 bpm; no hydrocephalus; 80< mean arterial pressure (MAP)<110 mmHg before intervention);
  3. patients with National Institutes of Health Stroke Scale (NIHSS) scores at admission ranging from 1 to 20;
  4. patients with total activity of living independence pre-stroke; and
  5. patients between 20 and 80 years old.

The exclusion criteria will be as follows:

  1. patients with mild to moderate deficits as described above (3);
  2. patients who are unable to complete the baseline survey because of serious aphasia, language difficulties, or cognitive deficits;
  3. patients with other medical conditions, such as severe heart failure, acute coronary syndrome, or lower-limb disorders, that prevent early mobilization; and
  4. patients who are unable to provide informed consent. In addition, we will exclude those showing rapid early deterioration of symptoms, as well as those with a concurrent diagnosis of rapidly deteriorating disease (e.g., terminal cancer).

Sites / Locations

  • National Taiwan University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

early mobilization

early standard intervention

Arm Description

early mobilization group will commence rehabilitation consisting of out-of-bed mobilization (including supine to sit training, sit on the edge of bed without supporting, standing with hand supporting, stepping while standing etc.)

early standard intervention included bed exercises including the joint range of motion exercise, bridge exercise, the straight leg raising exercise, stretching exercises, and the facilitation techniques during the period in a stroke center.

Outcomes

Primary Outcome Measures

the score-change of the Functional Independence Measure (FIM) assessment for daily living function
The functional independence of patient's capacities in terms of activity of daily living. The instrument assesses motor domain including dependence in self-care, sphincter management, transfer, locomotion as well as cognition domain including communication, social interaction and cognition.

Secondary Outcome Measures

the number of days required to reach a sitting>5 minutes milestone
The milestone will be the ability to sit on the edge of a bed with the feet touching the floor without support > 5 minutes.
the number of days required to reach a standing>1 minute milestone
The milestone will be the ability to stand without support for longer than 1 minute and with the feet freely positioned.
the number of days required to reach a walking>50 meters milestone using the functional ambulation category (FAC)
The milestone will consist of walking on a level surface for a minimum of 50 meters with/without an assistive device while under supervision or required support level
the number of serious adverse events
Immobility-related and neurological serious adverse events include both fatal and non-fatal complications; immobility-related events include pulmonary embolism, deep-vein thrombosis, urinary tract infection, pressure sores, pneumonia; and neurological events include stroke progression and recurrent stroke.
the score-change of the Postural Assessment Scale for Stroke Patients (PASS)
12 four-level items of varying difficulty with a maximum score of 36
the score-change of systolic blood pressure (SBP) during the acute phase
recorded the absolute SBP values over time
the number of days required to stay in the stroke center
the length of stay in the stroke center

Full Information

First Posted
September 10, 2017
Last Updated
April 10, 2019
Sponsor
National Taiwan University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03292211
Brief Title
The Effect of Early Mobilization in Mild to Moderate Hemorrhagic Stroke
Official Title
Comparing the Benefits of Functional Recovery Between the Early Mobilization and Early Conventional Intervention After Stroke for the Patients With Mild to Moderate Hemorrhagic Stroke
Study Type
Interventional

2. Study Status

Record Verification Date
September 2018
Overall Recruitment Status
Completed
Study Start Date
September 12, 2017 (Actual)
Primary Completion Date
November 9, 2018 (Actual)
Study Completion Date
February 10, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Taiwan University Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This study aims to examine the outcomes of early mobilization and early intervention within 24-72 hours after the onset of hemorrhagic stroke in patients admitted to an intensive care unit within 24 hours after stroke. The patients after hemorrhagic stroke who undergo early intervention only will be compared with those who also receive early mobilization in order to determine if the early mobilization intervention results in earlier or more effective recovery of postural stability, activities of daily living function, or motor capacity. The participants will be randomly assigned to the following two groups: (1) the early mobilization (+early rehabilitation) group and (2) the early rehabilitation group.The measurement parameters will be collected before the intervention (basic parameters), two weeks after the stroke, four weeks after the stroke and three months after the stroke. SPSS (version 17.0) will be used to carry out repeated measures analysis of variance (repeated ANOVA) to compare the differences between the groups at different time points (including basic values and follow-up values). For statistical significance, Bonferroni correction will be applied for the post-hoc analysis of the groups.
Detailed Description
Early intervention has been proven to enhance post-stroke functional recovery. Recent studies have proposed that early mobilization (out-of-bed activities) also contributes to an individual's functional improvement after stroke. However, studies on early intervention after stroke have mainly investigated patients with ischemic stroke, while tending to exclude patients with hemorrhagic stroke who were admitted to intensive care units. The main reason for this is the difference between hemorrhagic and ischemic strokes in terms of their mechanisms and treatment methods. Hemorrhagic stroke is characterized by higher severity and fatality rates, and there is a general lack of research on early rehabilitation and mobilization after hemorrhagic strokes. To our knowledge, there have been no previous studies that have simultaneously compared the impact of early mobilization and early rehabilitation starting at the same time on the motor recovery of patients after intracranial hemorrhage. Thus, this study aims to examine the outcomes of early mobilization and intervention within 24-72 hours after the onset of hemorrhagic stroke in patients admitted to an intensive care unit within 24 hours after stroke. The patients will be compared to identify differences in the recovery of postural stability and functional abilities two weeks, four weeks and three months after stroke. The participants will be randomly assigned to the following two groups: (1) the early mobilization (+early rehabilitation) group and (2) the early rehabilitation group. The early mobilization group will receive early mobilization intervention within24-72 hours after stroke while being monitored by medical equipment. In early mobilization group, this intervention program will most include early out-of-bed activities (that is, rolling and sitting at the edge of the bed). The early rehabilitation group will undergo only conventional early in-bed activities in the stroke center. All the outcome measures will be collected at baseline (pre-intervention), 2 weeks after stroke, 4 weeks after stroke and three months after stroke.The results will be analyzed with SPSS (IBM SPSS Statistics 17, Chicago, IL, USA). Repeated measures analysis of variance (repeated ANOVA) and the Chi-square test for categorical variables will be used for comparing the outcome data. If there are significant interactions, a post hoc test with Bonferroni correction will be used to examine group differences within a time condition. A p value < 0.05 will be considered statistically significant.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hemorrhagic Stroke
Keywords
Early mobilization, Acute stroke, Early intervention, Early mobilization therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
early mobilization
Arm Type
Experimental
Arm Description
early mobilization group will commence rehabilitation consisting of out-of-bed mobilization (including supine to sit training, sit on the edge of bed without supporting, standing with hand supporting, stepping while standing etc.)
Arm Title
early standard intervention
Arm Type
Other
Arm Description
early standard intervention included bed exercises including the joint range of motion exercise, bridge exercise, the straight leg raising exercise, stretching exercises, and the facilitation techniques during the period in a stroke center.
Intervention Type
Behavioral
Intervention Name(s)
early mobilization
Intervention Description
early out-of-bed activities including supine to sit training, sit on the edge of bed without supporting, standing with hand supporting, stepping while standing etc.within three days after stroke while being monitored by medical equipment.
Intervention Type
Behavioral
Intervention Name(s)
early standard intervention
Intervention Description
Conventional early in-bed activities within three days after stroke
Primary Outcome Measure Information:
Title
the score-change of the Functional Independence Measure (FIM) assessment for daily living function
Description
The functional independence of patient's capacities in terms of activity of daily living. The instrument assesses motor domain including dependence in self-care, sphincter management, transfer, locomotion as well as cognition domain including communication, social interaction and cognition.
Time Frame
baseline, 2-week, 4-week and three months after stroke
Secondary Outcome Measure Information:
Title
the number of days required to reach a sitting>5 minutes milestone
Description
The milestone will be the ability to sit on the edge of a bed with the feet touching the floor without support > 5 minutes.
Time Frame
baseline to within 3 months after stroke
Title
the number of days required to reach a standing>1 minute milestone
Description
The milestone will be the ability to stand without support for longer than 1 minute and with the feet freely positioned.
Time Frame
baseline to within 3 months after stroke
Title
the number of days required to reach a walking>50 meters milestone using the functional ambulation category (FAC)
Description
The milestone will consist of walking on a level surface for a minimum of 50 meters with/without an assistive device while under supervision or required support level
Time Frame
baseline to within 3 months after stroke
Title
the number of serious adverse events
Description
Immobility-related and neurological serious adverse events include both fatal and non-fatal complications; immobility-related events include pulmonary embolism, deep-vein thrombosis, urinary tract infection, pressure sores, pneumonia; and neurological events include stroke progression and recurrent stroke.
Time Frame
baseline to within 3 months after stroke
Title
the score-change of the Postural Assessment Scale for Stroke Patients (PASS)
Description
12 four-level items of varying difficulty with a maximum score of 36
Time Frame
baseline, 2-week, 4-week and three months after stroke
Title
the score-change of systolic blood pressure (SBP) during the acute phase
Description
recorded the absolute SBP values over time
Time Frame
up to 2 weeks after stroke
Title
the number of days required to stay in the stroke center
Description
the length of stay in the stroke center
Time Frame
baseline to within 3 months after stroke

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
The inclusion criteria will be as follows: patients with a first time intracerebral (either cortical or subcortical) hemorrhage with unilateral hemiparesis/ hemiplegia confirmed by magnetic resonance imaging or computed tomography; patients with no contraindications to being mobilized (early intervention) within 24 hours of stroke onset (based on the medical team's clinical judgment: including systolic blood pressure (SBP)<160mmHg in resting; resting heart rate (HR)<130 bpm; no hydrocephalus; 80< mean arterial pressure (MAP)<110 mmHg before intervention); patients with National Institutes of Health Stroke Scale (NIHSS) scores at admission ranging from 1 to 20; patients with total activity of living independence pre-stroke; and patients between 20 and 80 years old. The exclusion criteria will be as follows: patients with mild to moderate deficits as described above (3); patients who are unable to complete the baseline survey because of serious aphasia, language difficulties, or cognitive deficits; patients with other medical conditions, such as severe heart failure, acute coronary syndrome, or lower-limb disorders, that prevent early mobilization; and patients who are unable to provide informed consent. In addition, we will exclude those showing rapid early deterioration of symptoms, as well as those with a concurrent diagnosis of rapidly deteriorating disease (e.g., terminal cancer).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jiann-Shing Jeng
Organizational Affiliation
NTUH
Official's Role
Principal Investigator
Facility Information:
Facility Name
National Taiwan University Hospital
City
Taipei
ZIP/Postal Code
100
Country
Taiwan

12. IPD Sharing Statement

Citations:
PubMed Identifier
31858865
Citation
Yen HC, Jeng JS, Chen WS, Pan GS, Chuang Pt Bs WY, Lee YY, Teng T. Early Mobilization of Mild-Moderate Intracerebral Hemorrhage Patients in a Stroke Center: A Randomized Controlled Trial. Neurorehabil Neural Repair. 2020 Jan;34(1):72-81. doi: 10.1177/1545968319893294. Epub 2019 Dec 20.
Results Reference
derived

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The Effect of Early Mobilization in Mild to Moderate Hemorrhagic Stroke

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