Treatment Preference in Patients with NMOSD

JRCT ID: jRCT1030230308

Registered date:25/08/2023

Basic Information

• Recruitment status: Recruiting
• Health condition(s) or Problem(s) studied: Neuromyelitis Optica Spectrum Disorders
• Date of first enrollment: 03/08/2023
• Target sample size: 30
• Study type: Other

Outcome(s)

• Primary Outcome: causal Relationship between Subjective Adverse Event Experience and Impact on Daily Living of Patients with NMOSD
• Secondary Outcome: subjective Adverse Event Experience and Importance of Impact on Daily Living of Patients with NMOSD

Key inclusion & exclusion criteria

• Age minimum: >= 20age old
• Age maximum: Not applicable

Include criteria

Subjects who meet all of the following criteria:
(1)Documented diagnosis of NMOSD
(2)Anti-aquaporin-4 antibody test positive
(3)Patients who are taking or have taken an oral steroid
(4)Patients aged 20 years or older at the time of enrollment
(5)Must have sufficient understanding to conduct the research (The patient may require assistance in reading aloud, etc. due to visual disturbance.)
(6)Individuals who have consented to participate in this research
(7)Patients who are living in Japan at the time of enrollment
(8)Individuals who have equipment/communication environment to apply for research participation online and perform interviews or respond to questionnaires

Exclude criteria

Subjects who meet any of the following criteria:
(1)Patients who have difficulty in obtaining consent or conducting this research due to a lack of Japanese ability
(2)Patietnts who cannot participate in the survey

Related Information

• Primary Sponsor: Yamashita Katsuhisa
• Secondary Sponsor: Nishi Kazuhiko