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Altering Activation Patterns Post-stroke

Altering Activation Patterns in the Distal Upper Extremity After Stroke

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02418949
Enrollment
96
Registered
2015-04-17
Start date
2015-11-01
Completion date
2022-03-23
Last updated
2026-03-31

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

Conditions

Stroke, Muscle Spasticity, Hemiparesis

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

DRUGPlacebo 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

OTHERActive 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.

OTHERPassive 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.

Sponsors

Shirley Ryan AbilityLab
Lead SponsorOTHER
National Institutes of Health (NIH)
CollaboratorNIH
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
CollaboratorNIH

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

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

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

MeasureTime frameDescription
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

MeasureTime frameDescription
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

STUDY_DIRECTORDerek G Kamper, PhD

North Carolina State University

PRINCIPAL_INVESTIGATORElliot Roth, MD

Shirley Ryan AbilityLab

Participant flow

Participants by arm

ArmCount
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
Total94

Baseline characteristics

CharacteristicCyproheptadine + AMPPlacebo for Cyproheptadine + StretchingCyproheptadine + StretchingPlacebo for Cyproheptadine + AMPTotal
Age, Continuous60 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 Participants11 Participants19 Participants17 Participants63 Participants
Chedoke McMaster Scale of Hand
Equal or less than 2
6 Participants11 Participants6 Participants8 Participants31 Participants
Ethnicity (NIH/OMB)
Hispanic or Latino
1 Participants21 Participants23 Participants23 Participants68 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
21 Participants1 Participants2 Participants2 Participants26 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants0 Participants0 Participants
Fugl-Meyer Upper Extremity Assessment15 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 Participants7 Participants11 Participants12 Participants40 Participants
Lesion Side
Right
12 Participants15 Participants14 Participants13 Participants54 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
3 Participants0 Participants2 Participants1 Participants6 Participants
Race (NIH/OMB)
Black or African American
11 Participants9 Participants12 Participants13 Participants45 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants0 Participants0 Participants
Race (NIH/OMB)
White
8 Participants13 Participants11 Participants11 Participants43 Participants
Sex: Female, Male
Female
8 Participants9 Participants10 Participants8 Participants35 Participants
Sex: Female, Male
Male
14 Participants13 Participants15 Participants17 Participants59 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 typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
EG003
affected / at risk
deaths
Total, all-cause mortality
0 / 230 / 220 / 260 / 25
other
Total, other adverse events
19 / 2315 / 2218 / 2621 / 25
serious
Total, serious adverse events
2 / 232 / 221 / 260 / 25

Outcome results

Primary

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)

ArmMeasureValue (MEAN)
Cyproheptadine + AMPChange in Mean Completion Time for Graded Wolf Motor Function Test (GWMFT)-3.66 Seconds
Placebo for Cyproheptadine + StretchingChange in Mean Completion Time for Graded Wolf Motor Function Test (GWMFT)-0.51 Seconds
Cyproheptadine + StretchingChange in Mean Completion Time for Graded Wolf Motor Function Test (GWMFT)-4.00 Seconds
Placebo for Cyproheptadine + AMPChange in Mean Completion Time for Graded Wolf Motor Function Test (GWMFT)-3.89 Seconds
Secondary

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)

ArmMeasureValue (MEAN)
Cyproheptadine + AMPChange in Grip Relaxation Time (Following a Maximum Voluntary Contraction (MVC)-1.66 Seconds
Placebo for Cyproheptadine + StretchingChange in Grip Relaxation Time (Following a Maximum Voluntary Contraction (MVC)-0.96 Seconds
Cyproheptadine + StretchingChange in Grip Relaxation Time (Following a Maximum Voluntary Contraction (MVC)-1.06 Seconds
Placebo for Cyproheptadine + AMPChange in Grip Relaxation Time (Following a Maximum Voluntary Contraction (MVC)-2.65 Seconds

Source: ClinicalTrials.gov · Data processed: Apr 1, 2026