Assessing Relapse in Multiple Sclerosis (ARMS) Questionnaire (ARMS)
Assessing Relapse in Multiple Sclerosis (ARMS) Questionnaire - A Phase 4 Pilot Study
This Phase 4 pilot cross-sectional descriptive/exploratory study is to be conducted in clinical practice settings (including MS (Multiple sclerosis) specialty clinics, general neurology practices, or other academic or private practice settings) in the United States to assess the psychometric properties of the ARMS questionnaire in approximately 100 adult patients with MS who are experiencing a confirmed relapse, as identified by the investigator or designee at each site. Neither efficacy nor safety of treatment will be evaluated in this study.
The ARMS questionnaire is a 2-part, 2-page survey, with each part comprising 7 questions on 1 page. Part 1 is designed to evaluate the patient's relapse symptoms and how the symptoms affect daily activities and overall function, as well as patient's response to past treatments for previous relapses, as a means of guiding treatment selection. Part 2 is designed to evaluate treatment response in terms of symptom relief and functioning, as well as treatment tolerability. Part 1 of the survey is to be completed when the patient presents with new relapse of MS. Part 2 of the survey is to be completed 1 month (± 1 week) after initiation of treatment for relapse of MS. Treatment for relapse will be at the sole discretion of the investigator.
연구 개요
연구 유형
등록 (실제)
연락처 및 위치
연구 장소
-
-
Alabama
-
Birmingham, Alabama, 미국
- Tanner Center and Foundation for MS
-
-
California
-
Oceanside, California, 미국
- Neurology Center
-
-
Florida
-
Hollywood, Florida, 미국
- Infinity Clinical Research
-
Orlando, Florida, 미국
- McCare Center Neurology Services
-
-
Virginia
-
Fairfax, Virginia, 미국
- Neurology Center of Fairfax
-
-
참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
샘플링 방법
연구 인구
설명
Inclusion Criteria:
- Informed consent and HIPAA authorization must be obtained from the patient prior to any study-related procedures.
- Patient is ≥ 18 years of age at the time of participation
- Patient has confirmed MS relapse.
- Patient must have been treated with oral or IV corticosteroids for their previous relapse.
- Willingness to comply with all procedures and assessments.
Exclusion Criteria:
- Patient has pseudorelapse.
- Patient was treated with any therapies other than corticosteroids for their previous relapse.
- Any other condition which, in the opinion of the investigator, would not allow proper completion of this study.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
코호트 및 개입
그룹/코호트 |
개입 / 치료 |
|---|---|
|
ARMS Questionnaire Group
Patients with confirmed multiple sclerosis relapse who are willing to participate in the ARMS questionnaire.
These patients could not have been treated with any therapies other than oral or intravenous corticosteroids for their previous relapse.
|
The ARMS Questionnaire is a 2-part, 2-page survey, with each part comprising 7 questions on 1 page.
Eligible patients will be administered part 1 of the survey when the patient presents with new relapse.
Part 2 of the survey is to be completed 1 month (± 1 week) after initiation of treatment for relapse.
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Total Composite Score (TCS)
기간: After relapse treatment (1 month ± 1 week)
|
Total composite score is calculated from three interrelated questions on part 2 of the ARMS questionnaire (to be completed 1 month ± 1 week after relapse treatment).
|
After relapse treatment (1 month ± 1 week)
|
공동 작업자 및 조사자
스폰서
연구 기록 날짜
연구 주요 날짜
연구 시작
기본 완료 (실제)
연구 완료 (실제)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (추정)
연구 기록 업데이트
마지막 업데이트 게시됨 (추정)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
키워드
추가 관련 MeSH 약관
기타 연구 ID 번호
- QSC02-ARMS-01
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .
다발성 경화증에 대한 임상 시험
-
Sanko University완전한MULTİPLE SCLEROSİS | BALANCE | 유효성 | 신뢰도터키 (Türkiye)
-
University Hospital, Montpellier종료됨제1형 당뇨병 | Basal-bolus multiple-dily 인슐린 주사 | 인슐린 펌프(CSII)프랑스
ARMS Questionnaire에 대한 임상 시험
-
University Hospital, Toulouse완전한
-
T.C. ORDU ÜNİVERSİTESİMacquarie University, Australia모집하지 않고 적극적으로
-
Assistance Publique - Hôpitaux de Paris완전한
-
Centre Hospitalier Emile RouxUniversité Clermont-Auvergne, France아직 모집하지 않음
-
Cambridge University Hospitals NHS Foundation TrustUniversity of Cambridge알려지지 않은근골격계 질환 | 근골격계 부상
-
University of Toledo Health Science CampusProMedica Health System; The University of Toledo; ARMS Pharmaceutical LLC; Pediatric Pharmacology...빼는
-
First People's Hospital of Hangzhou완전한
-
University Hospital, Rouen아직 모집하지 않음