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. 2021 Oct 25;2021(10):CD012612. doi: 10.1002/14651858.CD012612.pub2

Dromerick 2009.

Study characteristics
Methods RCT
Adaptively randomised balancing age, NIHSS score, pretest ARAT, and days from stroke
Study compared 2 different CIMT protocols to control. For this Cochrane Review, we were interested in the 2 different protocols for CIMT only (excluding control)
Participants 52 participants in 3 study arms
Low CIMT:  n= 19; mean age 62.8 years; 68% female; 8.8 days poststroke
High CIMT: n = 16; mean age 64.5 years; 44% female; 9.9 days poststroke
Inpatient rehabilitation setting
Interventions Intervention was CIMT
Prespecified treatment (pre‐empted OT) based on Excite + RPT
Received extensive verbal and written feedback and review of prior day's achievements, day's goals and reinforcement of new gains and maintenance
Low CIMT: 2 hours of shaping therapy per day and padded constraint mitt for 6 hours per day
High CIMT: 3 hours of shaping therapy per day and padded constraint mitt for 90% of waking hours
Study treatment occurred 5 days per week for 2 weeks (consecutively)
Outcomes NIHSS
ARAT
FIM
SIS hand function subscale
Pain ratings
Geriatric Depression Scale
All measures were taken on baseline, at 14 days (postintervention) and at 90 days
Notes Conflict of interests:  authors disclosed the following:  Dr Dromerick has received research support from NIH, NINDS, and United States Veterans Affairs, and Intramural support from the United States Army, Department of Defense. Dr Lang has received research support from NIH, NINDS, and the Missouri Physical Therapy Association. Dr Miller has served on the Data and Safety Monitoring Board for Ethicon. Dr Powers has received research support from University of North Carolina, Washington University, University of Iowa, University of Kentucky, Harvard University, Bowdoin College, NIH, Legatus Emergency Services, LLC, Neutral, LLC, EDJ Associates, Hitchcock Foundation, Dartmouth‐Hitchcock Clinic, Certus International, Inc., Companion Baking Company, and Union Square Hospitality Group. Dr Wolf is supported by NIH, Allergan, and AMES
Funding: NIH grant 1 RO1 NS41261‐01A1 and James S. McDonnell Foundation grant 21002032