Quality of Life in Neuromuscular Disease
NCT02895763 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 159
Last updated 2016-09-23
Summary
A Quality work was conducted to enable the future construction of a Quality of Life Questionnaire Related to Health (HRQoL) in patients with slowly progressive neuromuscular disease (NMD) as myopathies and muscular dystrophies. The discussion group training is an effective method to perform a thorough investigation of aspects of HRQoL potentially altered by NMD. Patients were recruited in France by 4 reference centers MNMs. All verbal interactions between participants focus groups were recorded. A qualitative analysis of the transcript was performed. The transcript provided 2424 CIF categories. The results helped to identify and quantify aspects of life that are altered by NMDs between patients. A pool of 64 items and a validated questionnaire (the WHOQOLBREF) were thern passed by 159 patients enrolled in eight reference centers MNMs. The investigators constructed a questionnaire called QoLNMD which is composed of two general items and 24 items classified into three areas: (1) \\ Impact bodily symptoms, "(2) \\ Self-perception" and (3) \\ Activity participation. "Each area has good psychometric properties (Cronbach's alpha\> 0.77, test-retest ICC\> 0.81, H Loevinger\> 0.41) and met the assumptions of IRT. the comparison with the WHOQOL-BREF was used to assess similarities and differences with a generic questionnaire. The next step was to validate the QoLNMD reassessing its psychometric properties in a new patient sample and calibrate the IRT measurement system. The purpose of these new part of study was to validate the French version of the QoL-NMD on a confirmatory sample of patients and to calibrate its measurement system. A prospective study in 8 NMD referral centers (France) was conducted. Both the QoL-NMD and a validated generic questionnaire (the WHOQOLBREF) were administered to patients. 156 patients were included for the confirmatory psychometric analysis. All three domains showed adequate psychometric properties and met IRT assumptions. The IRT model calibration was then performed successfully on 315 patients. The French version of the QoL-NMD showed adequate psychometric properties and can be used in rehabilitation services. A conversion table enables easy transformation of sum scores into IRT-calibrated measures. Minimum detectable change tables help interpreting score change.
Conditions
- Quality of Life
- Muscular Dystrophies
Interventions
- OTHER
-
Form administrations
Sponsors & Collaborators
-
CHU de Reims
lead OTHER
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2006-06-30
- Primary Completion
- 2012-12-31
- Completion
- 2013-06-30
Countries
- France
Study Locations
More Related Trials
-
A Multicenter Phenotype-Genotype Analysis of LGMD Patients in China
NCT04989751 ·Status: ENROLLING_BY_INVITATION
-
Active NBS Study: Decentralised Monitoring Motor Development in Children With Duchenne Muscular Dystrophy or Spinal Muscular Atrophy Identified by Newborn Screening
NCT07286565 ·Status: RECRUITING ·Phase: NA
-
Long-Term Development of Muscular Dystrophy Outcome Assessments
NCT05989620 ·Status: RECRUITING
-
Outcome Measures in Duchenne Muscular Dystrophy: A Natural History Study
NCT02780492 ·Status: COMPLETED
-
Magnetic Resonance Imaging and Ultrasound Comparison With Load Evaluation
NCT06227182 ·Status: RECRUITING
-
A Patient Centric Motor Neuron Disease Activities of Daily Living Scale
NCT02852278 ·Status: COMPLETED
-
Evaluation of the Reproducibility of a Fatigability Test Fitted to Patients With Spinal Muscular Atrophy
NCT06562283 ·Status: RECRUITING ·Phase: NA
-
Endomysial Fibrosis, Muscular Inflammatory Response and Calcium Homeostasis Dysfunction in Duchenne Muscular Dystrophy
NCT01823783 ·Status: UNKNOWN ·Phase: NA
-
Quality of Life and Participation of the Adult with Spinal Muscular Atrophy in France
NCT05366465 ·Status: COMPLETED
-
Correlation Between Functional Capacity and Functional Capability in Duchenne Muscular Dystrophy
NCT05249361 ·Status: RECRUITING
-
Evaluation of Limb-Girdle Muscular Dystrophy
NCT00893334 ·Status: COMPLETED
-
Oxidative Capacity and Exercise Tolerance in Ambulatory SMA
NCT02895789 ·Status: COMPLETED
-
MAP THE SMA: a Machine-learning Based Algorithm to Predict THErapeutic Response in Spinal Muscular Atrophy
NCT05769465 ·Status: RECRUITING
-
Effects of NMES on Muscle Function of Patients With FSHD: a Double-blind Randomized Controled Clinical Trial
NCT02861911 ·Status: TERMINATED ·Phase: NA
-
Presymptomatic Neuromuscular Junction Defects and Compensatory Mechanisms in ALS
NCT03573466 ·Status: UNKNOWN ·Phase: NA
-
Natural History Study of Patients With Limb-Girdle Muscular Dystrophy 2I
NCT03842878 ·Status: COMPLETED
-
Digital Assessment of Speech and Fine Motor Control in ALS
NCT06315673 ·Status: RECRUITING
-
Diagnostic Journey, Patient Experience, and Disparities in the Treatment of Spinal Muscular Atrophy (SMA) in the MedStar Health System
NCT07223489 ·Status: RECRUITING
-
Clinical Determinants of Disease Progression in Patients With Limb Girdle Muscular Distrophy Type 2E
NCT04509609 ·Status: COMPLETED
-
Test-Retest Reliability of Pulmonary Function Tests in Patients With Duchenne's Muscular Dystrophy
NCT00207857 ·Status: WITHDRAWN
-
Electromyography to Diagnose Neuromuscular Disorders
NCT00004553 ·Status: COMPLETED ·Phase: NA
-
Non-invasive Imaging of Muscle Structure in Duchenne Muscular Dystrophy Using Multispectral Optoacoustic Tomography
NCT03490214 ·Status: COMPLETED ·Phase: NA
-
DMD Voice: Qualitative Interviews With Patients and Caregivers
NCT06925269 ·Status: RECRUITING
-
Neuromuscular Magnetic Stimulation in ALS Patients
NCT03618966 ·Status: COMPLETED ·Phase: PHASE2
-
Innovative Ultrasound Technology in Neuromuscular Disease
NCT02104921 ·Status: COMPLETED