跳至主要内容
临床试验/NCT06270342
NCT06270342已完成不适用

The Effect of Dual Task On Upper Extremity Functions In Multiple Sclerosis Patients

Kutahya Health Sciences University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2023年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
60
试验地点
1
主要终点
Beck Depression Scale

研究概览

简要总结

The primary aim of this study was to investigate the effect of dual tasking on upper extremity functions in individuals with multiple sclerosis (MS) and compare with healthy controls. Additionally, another aim of our study was to compare the cognitive status, quality of life, fatigue and emotional states of individuals with MS and healthy controls.

详细描述

The study was carried out at Kutahya Health Sciences University Evliya Çelebi Training and Research Hospital. 30 individuals with MS and 30 healthy controls, aged 18-65, were included in the study. In the evaluation, demographic and clinical data were recorded first. The Minnesota Manual Dexterity Test was used to evaluate the upper extremity function of the participants in single and dual task conditions, and the Dual Task Questionnaire was used to evaluate the difficulties experienced during dual tasks.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Other

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Having been diagnosed with Multiple Sclerosis for at least 1 year
  • •Being between the ages of 18-65
  • •Being at least a primary school graduate
  • •Volunteering to participate in the study
  • •EDSS score between 1 and 6.5

排除标准

  • •Patients whose Multiple Sclerosis diagnosis is uncertain
  • •Having additional neurological disease that may affect clinical evaluation
  • •Having a neurological and/or psychiatric disease that may affect cognitive tests
  • •Having had an attack in the last 3 months

结局指标

主要结局

Beck Depression Scale

时间窗: 10 minutes

Emotional Status Evaluation. The lowest score that can be obtained from the scale is 0 and the highest score is 63. According to the resulting total score; It results in absence-mild, mild-moderate, moderate-severe or severe.

The Minnesota Manual Dexterity Test

时间窗: 30 minutes

Upper Extremity Function Evaluation. The Minnesota Manual Dexterity Test basically consists of two subtests, the placement and translation test. Completing the test faster indicates better dexterity.

Dual Task Questionnaire

时间窗: 10 minutes

Dual Task Difficulty Evaluation. The survey consists of 10 items and is scored out of 5 points per question. A higher total score indicates worse dual task performance.

Edinburgh Handedness Questionnaire

时间窗: 10 minutes

Hand Preference Evaluation. The total scoring is between 100 and -100, individuals with more than 40 points are given right hand; Individuals in this score range from 40 to -40 inclusive are recorded as those who use both hands actively, and individuals with scores of -40 points and below are recorded as left-handed.

Expanded Disability Status Scale

时间窗: 10 minutes

Disability Status Evaluation. A score of 0 on the scale indicates normal neurological status, while a score of 10 means MS-related death.

Brief International Cognitive Assessment Battery for Multiple Sclerosis

时间窗: 15 minutes

Cognitive Status Evaluation. BICAMS comprises three tests, the Symbol Digit Modalities Test (SDMT), the learning trials of the California Verbal Learning Test II (CVLT-II), and the Brief Visuospatial Memory Test-Revised (BVMT-R).

Fatigue Impact Scale

时间窗: 5 minutes

Fatigue Status Evaluation. Each question receives a score between 0 (no problem) and 4 (maximum problem). The highest score is 160, and higher scores indicate fatigue.

Multiple Sclerosis Quality of Life Questionnaire-54

时间窗: 15 minutes

Quality of Life Status Evaluation. The survey contains 54 questions consisting of 12 sections. Added 18 questions are about; general quality of life (2 items), health stress (4 items), sexual functions and satisfaction (5 items), cognitive functions (4 items), energy (1 item), pain (1 item) and social functions (1 item).

次要结局

未报告次要终点

研究者

发起方
Kutahya Health Sciences University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Eda Ozge OKUR

Asst. Prof.

Kutahya Health Sciences University

研究点 (1)

Loading locations...

相似试验