Stroke, Muscle Spasticity, Hemiparesis
Conditions
Keywords
hand, rehabilitation, active movement training, passive cyclical stretching
Brief summary
This study evaluates a new rehabilitation approach for stroke survivors in the chronic phase of recovery in which the combination of drug therapy (cyproheptadine) and active movement practice (AMP) is used to encourage increased voluntary muscle control and strength.
Detailed description
In this four arm parallel design you will be randomly assigned to one of 4 groups: Group 1) cyproheptadine and active movement therapy, Group 2) placebo and active movement therapy, Group 3) cyproheptadine and passive stretching, or Group 4) placebo and passive stretching. The groups will be blinded so neither you nor the research staff (or even the study doctor) will know which drug (Cyproheptadine or placebo) you receive. Only the RIC pharmacist will have access to this information until all participants complete the entire study. Although you and the research staff administering the training sessions will know if you have been assigned to the active movement practice (AMP) or passive cyclical stretching group, it is important not to discuss this information with the rater (evaluator) or the study doctor. Cyproheptadine is an anti-serotonergic and anti spastic agent. It is expected to reduce the unwanted muscle hyper excitability (one measure of spasticity) common after stroke. During the course of the treatment you will be required to make several visits per week to RIC to either be evaluated or participate in the treatment sessions. Evaluations last approximately 2 hours and will be performed at the beginning of weeks 1, 2, 3 and 4, during the middle of treatment (beginning of week 7), at the end of training (beginning of week 10) as well as a final follow-up visit one month after the end of treatment (beginning of week 14). The training sessions will occur from weeks 4 through week 9 and will involve 1.5-hr. sessions (1 hr training plus setup time) 3 times per week. The investigators hypothesize that the group receiving the combined cyproheptadine and active movement therapy will have better outcomes than the groups receiving cyproheptadine or active movement therapy alone.
Interventions
Cyproheptadine will be titrated up to the chronic dose prior to involvement in hand therapy as well as gradually down to zero in the two weeks following treatment. Week 1 dose: 4mg taken twice daily (orally) Week 2 dose: 8mg taken twice daily (orally) Week 3 dose: (chronic dose): 8 mg taken three times daily (orally). Week 4-9: (chronic dose): 8 mg taken three times daily (orally). Week 10: 8 mg taken twice daily (orally). Week 11: 4 mg taken twice daily (orally). Week 12: no drug
Cyproheptadine will be titrated up to the chronic dose prior to involvement in hand therapy as well as gradually down to zero in the two weeks following treatment. Week 1 dose: 4mg taken twice daily (orally) Week 2 dose: 8mg taken twice daily (orally) Week 3 dose: (chronic dose): 8 mg taken three times daily (orally). Week 4-9: (chronic dose): 8 mg taken three times daily (orally). Week 10: 8 mg taken twice daily (orally). Week 11: 4 mg taken twice daily (orally). Week 12: no drug
Participants will alternate between active training with a custom video game and a robot active-assistive Voice and EMG-Driven Actuated (VAEDA) glove during active training occupational therapy.
Participants will wear the actuated device/glove for the duration of the training sessions (2 20-min stints followed by 10 min of rest) during which time the actuated glove will cyclically stretch the joints of the digits in the hand between flexion and extension while remaining passive/relaxed.
Sponsors
Study design
Eligibility
Inclusion criteria
* Chronic, severe hand hemiparesis resulting from a single stroke (Chedoke- McMaster Stroke Assessment: Stage of Hand 2 or 3) * Single stroke occurring at least 6 months prior to enrollment * Spasticity * Capacity to provide informed consent
Exclusion criteria
* Excessive pain in paretic upper limb * Hemispatial neglect (as assessed by the Behavioral Inattention Test) * Apraxia (as assessed by the FABERS battery) * Botulinum toxin injection in the upper extremity within the past 6 months * Introduction of new anti-spasticity medication within the past 6 months * Orthopaedic impairments * History of seizure disorder * Other major health impairment
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change in Mean Completion Time for Graded Wolf Motor Function Test (GWMFT) | baseline and 9 weeks (immediately post intervention) | GWMFT is a clinical outcome measure comprised of 15 timed tasks focusing on upper extremity function. Maximum allowable time per task is 120 seconds. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change in Grip Relaxation Time (Following a Maximum Voluntary Contraction (MVC) | baseline and 9 weeks (immediately post intervention) | Following a maximum voluntary contraction (MVC) -- Time (s) required for muscle electromyographic (EMG) signals to reduce to within 3 SD of pre-MVC EMG activity. |
Countries
United States
Contacts
North Carolina State University
Shirley Ryan AbilityLab
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| Cyproheptadine + AMP Cyproheptadine will be titrated up to the chronic dose prior to involvement in hand therapy.
Week 1 dose: 4mg taken twice daily (orally) Week 2 dose: 8mg taken twice daily (orally) Week 3 dose: (chronic dose): 8 mg taken three times daily (orally). Chronic dose will be maintained throughout the 6 weeks of Active movement practice (AMP) treatment (1 hour sessions 3x/week). Dose will be titrated down to zero in the 2 weeks following treatment.
Cyproheptadine: Cyproheptadine will be titrated up to the chronic dose prior to involvement in hand therapy as well as gradually down to zero in the two weeks following treatment.
Week 1 dose: 4mg taken twice daily (orally) Week 2 dose: 8mg taken twice daily (orally) Week 3 dose: (chronic dose): 8 mg taken three times daily (orally). Week 4-9: (chronic dose): 8 mg taken three times daily (orally). Week 10: 8 mg taken twice daily (orally). Week 11: 4 mg taken twice daily (orally). Week 12: no drug
Active Movement Practice (AMP): Participants will alternate between active training with a custom video game and a robot active-assistive Voice and EMG-Driven Actuated (VAEDA) glove during active training occupational therapy. | 22 |
| Placebo for Cyproheptadine + Stretching Placebo for Cyproheptadine will be titrated up to the chronic dose prior to involvement in hand therapy.
Week 1 dose: 4mg taken twice daily (orally) Week 2 dose: 8mg taken twice daily (orally) Week 3 dose: (chronic dose): 8 mg taken three times daily (orally). Chronic dose will be maintained throughout the 6 weeks of passive cyclical stretching treatment (1 hour sessions 3x/week). Each session will involve 20 min of stretching followed by 10 minutes of rest.
Dose will be titrated down to zero in the 2 weeks following treatment.
Placebo for Cyproheptadine: Cyproheptadine will be titrated up to the chronic dose prior to involvement in hand therapy as well as gradually down to zero in the two weeks following treatment.
Week 1 dose: 4mg taken twice daily (orally) Week 2 dose: 8mg taken twice daily (orally) Week 3 dose: (chronic dose): 8 mg taken three times daily (orally). Week 4-9: (chronic dose): 8 mg taken three times daily (orally). Week 10: 8 mg taken twice daily (orally). Week 11: 4 mg taken twice daily (orally). Week 12: no drug
Passive Cyclical Stretching: Participants will wear the actuated device/glove for the duration of the training sessions (2 20-min stints followed by 10 min of rest) during which time the actuated glove will cyclically stretch the joints of the digits in the hand between flexion and extension while remaining passive/relaxed. | 22 |
| Cyproheptadine + Stretching Cyproheptadine will be titrated up to the chronic dose prior to involvement in hand therapy.
Week 1 dose: 4mg taken twice daily (orally) Week 2 dose: 8mg taken twice daily (orally) Week 3 dose: (chronic dose): 8 mg taken three times daily (orally). Chronic dose will be maintained throughout the 6 weeks of passive cyclical stretching treatment (1 hour sessions 3x/week). Each session will involve 20 min of stretching followed by 10 minutes of rest.
Dose will be titrated down to zero in the 2 weeks following treatment.
Cyproheptadine: Cyproheptadine will be titrated up to the chronic dose prior to involvement in hand therapy as well as gradually down to zero in the two weeks following treatment.
Week 1 dose: 4mg taken twice daily (orally) Week 2 dose: 8mg taken twice daily (orally) Week 3 dose: (chronic dose): 8 mg taken three times daily (orally). Week 4-9: (chronic dose): 8 mg taken three times daily (orally). Week 10: 8 mg taken twice daily (orally). Week 11: 4 mg taken twice daily (orally). Week 12: no drug
Passive Cyclical Stretching: Participants will wear the actuated device/glove for the duration of the training sessions (2 20-min stints followed by 10 min of rest) during which time the actuated glove will cyclically stretch the joints of the digits in the hand between flexion and extension while remaining passive/relaxed. | 25 |
| Placebo for Cyproheptadine + AMP Placebo for Cyproheptadine will be titrated up to the chronic dose prior to involvement in hand therapy.
Week 1 dose: 4mg taken twice daily (orally) Week 2 dose: 8mg taken twice daily (orally) Week 3 dose: (chronic dose): 8 mg taken three times daily (orally). Chronic dose will be maintained throughout the 6 weeks of Active movement practice (AMP) treatment (1 hour sessions 3x/week). Dose will be titrated down to zero in the 2 weeks following treatment.
Placebo for Cyproheptadine: Cyproheptadine will be titrated up to the chronic dose prior to involvement in hand therapy as well as gradually down to zero in the two weeks following treatment.
Week 1 dose: 4mg taken twice daily (orally) Week 2 dose: 8mg taken twice daily (orally) Week 3 dose: (chronic dose): 8 mg taken three times daily (orally). Week 4-9: (chronic dose): 8 mg taken three times daily (orally). Week 10: 8 mg taken twice daily (orally). Week 11: 4 mg taken twice daily (orally). Week 12: no drug
Active Movement Practice (AMP): Participants will alternate between active training with a custom video game and a robot active-assistive Voice and EMG-Driven Actuated (VAEDA) glove during active training occupational therapy. | 25 |
| Total | 94 |
Baseline characteristics
| Characteristic | Cyproheptadine + AMP | Placebo for Cyproheptadine + Stretching | Cyproheptadine + Stretching | Placebo for Cyproheptadine + AMP | Total |
|---|---|---|---|---|---|
| Age, Continuous | 60 years STANDARD_DEVIATION 8.1 | 57.1 years STANDARD_DEVIATION 11.2 | 58.9 years STANDARD_DEVIATION 13.1 | 57.3 years STANDARD_DEVIATION 9.5 | 58.3 years STANDARD_DEVIATION 10.6 |
| Chedoke McMaster Scale of Hand Equal or Greater than 3 | 16 Participants | 11 Participants | 19 Participants | 17 Participants | 63 Participants |
| Chedoke McMaster Scale of Hand Equal or less than 2 | 6 Participants | 11 Participants | 6 Participants | 8 Participants | 31 Participants |
| Ethnicity (NIH/OMB) Hispanic or Latino | 1 Participants | 21 Participants | 23 Participants | 23 Participants | 68 Participants |
| Ethnicity (NIH/OMB) Not Hispanic or Latino | 21 Participants | 1 Participants | 2 Participants | 2 Participants | 26 Participants |
| Ethnicity (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Fugl-Meyer Upper Extremity Assessment | 15 Score STANDARD_DEVIATION 8.1 | 12.9 Score STANDARD_DEVIATION 5.5 | 16.1 Score STANDARD_DEVIATION 7.1 | 15.6 Score STANDARD_DEVIATION 5.6 | 15 Score STANDARD_DEVIATION 6.6 |
| Lesion Side Left | 10 Participants | 7 Participants | 11 Participants | 12 Participants | 40 Participants |
| Lesion Side Right | 12 Participants | 15 Participants | 14 Participants | 13 Participants | 54 Participants |
| Race (NIH/OMB) American Indian or Alaska Native | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Asian | 3 Participants | 0 Participants | 2 Participants | 1 Participants | 6 Participants |
| Race (NIH/OMB) Black or African American | 11 Participants | 9 Participants | 12 Participants | 13 Participants | 45 Participants |
| Race (NIH/OMB) More than one race | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) White | 8 Participants | 13 Participants | 11 Participants | 11 Participants | 43 Participants |
| Sex: Female, Male Female | 8 Participants | 9 Participants | 10 Participants | 8 Participants | 35 Participants |
| Sex: Female, Male Male | 14 Participants | 13 Participants | 15 Participants | 17 Participants | 59 Participants |
| Time Since Stroke onset (Years) | 5.9 years STANDARD_DEVIATION 4.3 | 5.4 years STANDARD_DEVIATION 5.3 | 5.6 years STANDARD_DEVIATION 4.7 | 8.5 years STANDARD_DEVIATION 8.6 | 6.4 years STANDARD_DEVIATION 6 |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk | EG002 affected / at risk | EG003 affected / at risk |
|---|---|---|---|---|
| deaths Total, all-cause mortality | 0 / 23 | 0 / 22 | 0 / 26 | 0 / 25 |
| other Total, other adverse events | 19 / 23 | 15 / 22 | 18 / 26 | 21 / 25 |
| serious Total, serious adverse events | 2 / 23 | 2 / 22 | 1 / 26 | 0 / 25 |
Outcome results
Change in Mean Completion Time for Graded Wolf Motor Function Test (GWMFT)
GWMFT is a clinical outcome measure comprised of 15 timed tasks focusing on upper extremity function. Maximum allowable time per task is 120 seconds.
Time frame: baseline and 9 weeks (immediately post intervention)
| Arm | Measure | Value (MEAN) |
|---|---|---|
| Cyproheptadine + AMP | Change in Mean Completion Time for Graded Wolf Motor Function Test (GWMFT) | -3.66 Seconds |
| Placebo for Cyproheptadine + Stretching | Change in Mean Completion Time for Graded Wolf Motor Function Test (GWMFT) | -0.51 Seconds |
| Cyproheptadine + Stretching | Change in Mean Completion Time for Graded Wolf Motor Function Test (GWMFT) | -4.00 Seconds |
| Placebo for Cyproheptadine + AMP | Change in Mean Completion Time for Graded Wolf Motor Function Test (GWMFT) | -3.89 Seconds |
Change in Grip Relaxation Time (Following a Maximum Voluntary Contraction (MVC)
Following a maximum voluntary contraction (MVC) -- Time (s) required for muscle electromyographic (EMG) signals to reduce to within 3 SD of pre-MVC EMG activity.
Time frame: baseline and 9 weeks (immediately post intervention)
| Arm | Measure | Value (MEAN) |
|---|---|---|
| Cyproheptadine + AMP | Change in Grip Relaxation Time (Following a Maximum Voluntary Contraction (MVC) | -1.66 Seconds |
| Placebo for Cyproheptadine + Stretching | Change in Grip Relaxation Time (Following a Maximum Voluntary Contraction (MVC) | -0.96 Seconds |
| Cyproheptadine + Stretching | Change in Grip Relaxation Time (Following a Maximum Voluntary Contraction (MVC) | -1.06 Seconds |
| Placebo for Cyproheptadine + AMP | Change in Grip Relaxation Time (Following a Maximum Voluntary Contraction (MVC) | -2.65 Seconds |