Phase 2
N=13
Pilot Trial of Botulinum Toxin and Occupational Therapy for Writer's Cramp
Dystonia
Bottom Line
View on ClinicalTrials.gov: NCT02015039 ↗Enrolled (actual)
13
Serious AEs
0.0%
Results posted
Jan 2018
Primary outcome: Primary: Using a Patient Rated Subjective Scale (Visual Analogue Scale), Change From Baseline With Botulinum Toxin Therapy Plus Occupational Therapy Compared to Botulinum Toxin Therapy Alone at 20 Weeks. — -20.6; -41.6 percentage of change
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 2
- Interventions
- BoNT Injections (Drug); Occupational Therapy (Procedure)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- National Institute of Neurological Disorders and Stroke (NINDS)
- Primary completion
- Sep 2016
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Using a Patient Rated Subjective Scale (Visual Analogue Scale), Change From Baseline With Botulinum Toxin Therapy Plus Occupational Therapy Compared to Botulinum Toxin Therapy Alone at 20 Weeks. |
-20.6; -41.6 | — |
| SECONDARY Change in the Writers Cramp Rating Scale (WCRS) From Baseline to Week 20 in Participants Receiving Botulinum Toxin Therapy Alone Compared With Botulinum Toxin Therapy Plus Occupational Therapy. |
46; -20.18 | — |
| SECONDARY Change on the Writer's Cramp Impairment Scale (WCIS) Score From Baseline to 20 Weeks. |
7.61; -34.13 | — |
| SECONDARY Change on the Writer's Cramp Disability Scale (WCDS) Score From Baseline to 20 Weeks. |
-41.5; -35.6 | — |
| SECONDARY Change in Hand Grip Strength From Baseline to 20 Weeks Following Botulinum Toxin Therapy Alone and Botulinum Toxin Therapy Plus Occupational Therapy. |
7.49; -9.00 | — |
| SECONDARY Change in Quantitative Writing Metrics Obtained Via Numerical Analyses of Writing Samples Using a Digitizing Tablet. |
25.76; -0.91 | — |
| SECONDARY Using a Patient Rated Subjective Scale (Visual Analogue Scale), Change From Baseline With Botulinum Toxin Therapy Plus Occupational Therapy Compared to Botulinum Toxin Therapy Alone at 24 Weeks. |
-2.12; -2.0 | — |
Summary
Objective: Writer s cramp (WC) is a form of focal hand dystonia (FHD). Focal injections of botulinum toxin (BoNT) are the current best therapy. Past studies showed that some types of rehabilitative therapy can be useful. The hypothesis of this study is that BoNT together with a specific type of occupational therapy will be better than BoNT alone for treating these patients. Additionally, studies on WC were hampered by the lack of objective, validated rating scales. In this pilot study, we will assess the value of a new scale compared with older scales.
Study population: The study population will consist of 12 WC patients (accrual ceiling of 16).
Design: Patients will be randomized so that 6 patients will receive just BoNT therapy and 6 patients will receive BoNT therapy plus occupational therapy. The physical therapy will involve specific exercises of finger movements in the direction opposite to the patient s own dystonic movements, during the writing task. The movements will be isometric against splints made to suit the individual patient. The final outcome will be assessed after 20 weeks of treatment. Patients will be evaluated on several scales, including the writer s cramp rating scale (WCRS) and writer s cramp impairment scale (WCIS), and will also be videotaped. The primary outcome will be based on patient reported subjective scale and the secondary outcomes will be assessed by four blinded raters of the videotapes, done both before and after treatment.
Outcome measures: The primary outcome is to show additional improvement from baseline with BoNT therapy plus occupational therapy compared to BoNT alone at 20 weeks using a patient-rated subjective scale. The secondary outcomes are to show improvement in scores of WCRS, WCIS, WCDS, and writing parameters with a new handwriting analysis program. Additionally, the scores obtained from WCRS and WCIS will be compared.
Eligibility Criteria
- INCLUSION CRITERIA
- be at least 18 years of age
- have writer s cramp
- patients are enrolled in 93-N-0202 and 85-N-0195
- willing to be videotaped while writing
- have normal hand function other than FHD
- be willing to use therapeutic daily rehabilitative therapies as prescribed
- have some positive subjective response to BoNT demonstrated on at least two prior treatments
- be able to comprehend and perform the daily activities required for those who are involved in combined therapy.
EXCLUSION CRITERIA
- BoNT administration within 3 months of participation
- No response to BoNT
- Unable to provide consent
- Patients taking oral medications for WC including muscle relaxants or other centrally-active medications such as antidepressants which may enhance tremors
- Medical conditions that affect hand function, such as stroke, nerve entrapment, tremor, parkinsonism, chorea, ataxia affecting the dominant hand
- Unable to provide consent
Data sourced from ClinicalTrials.gov (NCT02015039). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.