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Sms Guided Training After Acute Stroke

Sms Guided Training After Acute Stroke: A Pilot Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02720276
Acronym
StrokeWalk
Enrollment
19
Registered
2016-03-25
Start date
2015-10-31
Completion date
2016-06-30
Last updated
2017-09-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Stroke

Keywords

stroke, exercise, walking, mobility

Brief summary

The purpose of this exploratory study is to investigate how a predetermined outdoor walking program (12 weeks) is best delivered to individuals with stroke over 18 years, either by smartphone and the Short Message Service (SMS) or video link. Furthermore, the aim is to investigate how the study design works in practice and determine the effects of the outdoor walking exercise program in combination with a leg exercise on physical functioning (walking capacity, gait speed, mobility and grip strength).

Detailed description

Twenty community-living individuals in Uppsala municipality will be included and treated with a cross-over design. Ten individuals will initially receive exercise instructions to their smartphones via Short Message Service (SMS) for 6 weeks and after that instructions by a video link (6 weeks). Another 10 individuals will initially receive instructions by a video link and then switching to management with SMS after 6 weeks of training. Intervention: Participants are supposed to perform an outdoor walking exercise program for 12 weeks. The walks should gradually increase in frequency and intensity, and is expected to start after discharge from the stroke department, after the assessment. The first 2 weeks start with daily walks. The walks will be conducted at a pace that increases the heart rate but still makes it possible to talk. The intensity and frequency of walks will progressively increase performed according to the Borg scale: 12-15, ie, moderate to strenuous. Participants will walk 5-7 days/week. Added to this is a strength exercise, which should be performed in connection with the walk training. Methods: Questionnaires and medical records used for documentation of age, sex, comorbidity, blood pressure, medications and previous education. Assessment of motor function, cognition, level of physical activity are only performed as screening at baseline measurements. Objective evaluation of the participants' adherence to the outdoor walking program will be measured with a training diary where the individual documents whether they have followed the training instructions. Power analysis is not performed since this is an exploratory study. The investigators will analyze the data using an intention-to -treat. The investigators will also do a 'per-protocol analysis, where only participants who completed the training are included. Participants should have participated in at least 50% of the training sessions. All analyzes will be done using SPSS version 23 (IBM, Armonk).

Interventions

OTHERTraining after acute stroke

Outdoor walking: Participants will receive daily training instructions via Short message Service (SMS) over 12 weeks. The walks are increased in frequency and intensity. The intensity are rated using the Borg scale to 12-15. The first 2 weeks begins with daily walks of 10 minutes. The last 4 weeks the walk training will partly be performed in intervals in combination with conventional outdoor walks. The interval training includes warming-up (5 minutes), fast walking for 4 minutes alternated with slower walking for three minutes. This is repeated 3 times, followed by cooling down for about five minutes. Strength training: to repeatedly get up from sitting. Number of repetitions will increase from 5-20 per set and will be performed daily in 3 sets with a short rest between each set.

Sponsors

Uppsala County Council, Sweden
Lead SponsorOTHER_GOV

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. ≥ 18 years 2. Verified ischemic cerebral infarction or intracerebral hemorrhage. 3. Sufficient walking capacity and motor function 4. Able to communicate in Swedish 5. Signed consent

Exclusion criteria

Are one or more of the following: 1. Subarachnoid bleeding 2. Insufficient cognition and impaired ability to understand instructions 3. Medical problems that make it unsuitable to participate

Design outcomes

Primary

MeasureTime frameDescription
6 Minutes Walk Testchange from baseline walking capacity to three monthswalking capacity

Secondary

MeasureTime frameDescription
Saltin Grimby Physical Activity Level Scalebaselinelevel of physical activity
Jamar hand dynamometerchange from baseline hand-grip strength to three monthshand-grip strength
The Visual Analogue Rating Scale (VAS)change from six baseline to three months.Report of how to deliver the best instructions.
Short Physical Performance Batterychange from baseline mobility to three monthsmobility
10 meters walk testchange from baseline gait speed to three monthsgait speed
Montreal Outcome Assessmentbaselinecognitive function
Modified Rankin Scalebaselinemotor function

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026