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The Application of Thermal Stimulation on Functional Recovery of Stroke Patients

The Application of Thermal Stimulation on Functional Recovery of Stroke Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01418404
Enrollment
220
Registered
2011-08-17
Start date
2010-01-31
Completion date
2014-12-31
Last updated
2015-04-08

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

Conditions

Stroke

Keywords

Stroke, Effects of TS in U/E motor recovery, Brain mapping, Kinematics analysis

Brief summary

In literature review, thermal stimulation (TS) intervention is effective in facilitating upper extremity functional recovery in stroke patients. In addition, several functional MRI studies have indicated that thermal stimuli promoted activation in the premotor and motor cortices of healthy participants. These imply the possibility of TS in cortical reorganization. However, there were no studies exploring the relationship of the TS intervention and cortical reorganization. By the functional recovery of stroke patients, findings of brain image and brain mapping, it could enhance the understanding the TS influences on brain reorganization. Regarding with clinical application of the TS intervention for improving functional performance of upper extremity in participants with stroke, the best parameters of TS intervention in clinical practice have not been decided. Therefore, this five-year study recruited three groups of stroke patients (acute, sub-acute, chronic) undergoing TS intervention with different parameters. Functional scales, kinematic data, brain image were taken in several timelines as outcome measures.

Detailed description

The thermal stimulation (TS) intervention uses the heat and cold apply alternately (\ 30minutes), and this kind temperature application is common in clinical neuromuscular or sports rehabilitation. Moreover, some studies have proved efficacy of the TS on stroke. However, the best parameters and application on different-stage stroke groups have not been clearly explored. Moreover, in order to discover the TS intervention influences on neuroplasticity, the brain images and the brain mapping are taken in the group A (explained in the below). In addition, the kinematic data was also collected in group A. However, the above-mentioned three examination are optional. Finally, functional recovery measurements (clinical scales) are measured in the three groups. There are three groups (90 participants in each group) and their respective TS intervention design. In other word, three sub-studies (A, B, C) are under this project. Group A recruited 90 acute stroke (\ 30 days) and the independent variable is temperature of TS intervention. Group B is with sub-acute stroke (3-12 months), undergoing different frequency of TS intervention. Group C targets on participants with chronic stroke (\> 1 y/o) and this variation in TS is intensity of TS application (30 mins vs 60 mins/each session).

Interventions

OTHERNoxious TS

hot, cold alternately, noxious TS in study A

OTHERInnocuous TS

warm, cool alternately, Innocuious TS in study A

OTHERHigh Frequency of Noxious TS

High Frequency of Noxious TS in study B

OTHERLow Frequency of Noxious TS

Low Frequency of Noxious TS in study B

OTHERHigh Intensity of Noxious TS

High Intensity of Noxious TS in study C

OTHERLow Intensity of Noxious TS

Low Intensity of Noxious TS in study C

Sponsors

E-DA Hospital
CollaboratorOTHER
Kaohsiung Municipal Hsiaokang Hospital
CollaboratorOTHER_GOV
Kaohsiung Medical University Chung-Ho Memorial Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. first-ever ischemic stroke; 2. no severe cognitive impairments and able to follow instructions; 3. sit on a chair for more than 30 minutes independently.

Exclusion criteria

1. musculoskeletal or cardiac disorders that potentially interferes with experimental tests; 2. diabetic or sensory impairment that attributable to peripheral vascular disease or neuropathy; 3. speech disorder or global aphasia; 4. skin problems at the sites of stimulation; 6.contraindications of heat or ice application.

Design outcomes

Primary

MeasureTime frameDescription
Movement performance assessmentbaseline, half time-line of whole intervention period, post-intervention, 1 month follow-up, 6 month follow-up* Movement performance assessment by clinical motor assessment scales in upper extremity * executed by qualified physiotherapy * in study A, B, C
Brain imagesimmediate effects in 3 timeline* intermediate effect of TS means: pretest of the single TS, then application of this single TS, finally post-test of this TS in the session in the same day * immediate effects of intervention in the 1st day and 24th of intervention, six-month follow-up * this examination is optional * in study A. * use regular scan examination of hospital and operated by trained qualified professionals, the attending is consulted * This examination can be stopped at any time if participants do not want to perform or feeling unwell
Mapping of brain corteximmediate effect in four timeline* intermediate effect of TS means: pretest of the single TS, then application of this single TS, finally post-test of this TS in the session in the same day * immediate effects of intervention in the 1st day and 24th of intervention, one-month follow-up, six-month follow-up * in study A. * this examination is optional * use equipment of brain mapping and operated under trained staff, the attending is consulted This examination can be stopped at any time if participants do not want to perform or feeling unwell
Kinematics measure of upper extremity movementfour timeline* 1st day and 24th of intervention, one-month follow-up, six-month follow-up (This examination is optional) * signal emission marks are sticked on surface skin during motion tests * this examination is optional --in study A. * executed by trained qualified physiotherapy

Secondary

MeasureTime frameDescription
Quality of lifebaseline, post-intervention, 6 month follow-up* Quality of life by subjective questionnaires * executed by qualified physiotherapy --in study A, B, C.

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 19, 2026