Clinical Application of the Hanger Reflex to the Treatment of Cervical Dystonia

Clinical Application of the Hanger Reflex to the Treatment of Cervical Dystonia - Treatment of Cervical Dystonia by Hanger reflex

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000007772

Enrollment

Registered

2012-04-16

Start date

2012-04-01

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

Spasmodic torticolli (Cervical dystonia)

Interventions

Put on the device for more than 30 minutes per day For three months

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients diagnosed as the cervical dystonia with mainly rotated symptom.

Exclusion criteria

Exclusion criteria: Patients who don't have the Hanger reflex. Patients whose medication might be changed due to unstableness of their clinical condition.

Design outcomes

Primary

Measure	Time frame
Evaluate by Toronto Western Spasmodic Torticollis Rating Scale and modified Tsui score after applying the portable device for 3 months.	—

Countries

Japan

Contacts

Public ContactTakashi Asahi

Toyama university hospital Department of Neurosurgery

takashi-tym@umin.ac.jp076-434-7348

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026