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Validation of TU-NMS questionnaire, prevalence, and benefit of botulinum toxin injection on non-motor symptoms in primary craniocervical dystonia

Validation of TU-NMS questionnaire, prevalence, and benefit of botulinum toxin injection on non-motor symptoms in primary craniocervical dystonia

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20251124004
Enrollment
26
Registered
2025-11-24
Start date
2023-01-01
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Patients enrolled in this study must be age over 18 years and were diagnosed with CCD by neurologists according to the diagnostic criteria. Patients with significant cognitive impairment, secondary dystonia, generalized dystonia, focal limb dystonia, deep brain stimulation, and illiteracy were excluded from the study. The patient should not been treated with BoTN injection within the last 3 months prior to the first assessment. Craniocervical dystonia, dystonia, non-motor symptoms

Interventions

Botulinum toxin injections were administered to affected craniofacial or cervical muscles. Patients were assessed before and one month after injection for changes in non-motor symptoms, quality of lif
Experimental Procedure/Surgery

Sponsors

None listed

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Participants who 1. visited the Botulinum Toxin (BoNT) clinic at Thammasat University Hospital between January and December 2023 2. were aged over 18 years 3. were diagnosed with craniocervical dystonia (CCD) by neurologists according to established diagnostic criteria

Exclusion criteria

Exclusion criteria: Patients 1. with significant cognitive impairment 2. with secondary dystonia 3. with generalized dystonia 4. with focal limb dystonia 5. who had undergone deep brain stimulation 6. who were illiterate 7. who had recieved with BoTN injection within the last 3 months prior to the first assessment

Design outcomes

Primary

MeasureTime frame
Validation of TU-NMSQuest (construct and concurrent validity) at baseline Spearman rank correlation

Secondary

MeasureTime frame
Efficacy of BoTN injection on non-motor symptoms of CCD 1 month after botulinum toxin injection McNemar test

Countries

Thailand

Contacts

Public ContactPraween Lolekha

Thammasat University

pwlolekha@gmail.com0814461487

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Apr 4, 2026