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Limb-Girdle Muscular Dystrophy Type 2I in Norway

Limb-Girdle Muscular Dystrophy Type 2I in Norway - a Cohort Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03930628
Enrollment
106
Registered
2019-04-29
Start date
2020-01-06
Completion date
2023-06-30
Last updated
2022-11-07

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

Conditions

Limb Girdle Muscular Dystrophy, Limb Girdle Muscular Dystrophy R9 FKRP-related, Limb Girdle Muscular Dystrophy, Type 2I, Muscular Dystrophies

Brief summary

Key goals are to establish the natural history of limb-girdle muscular dystrophy type 2I (LGMD 2I) and identify feasible and sensitive tools and biomarkers to measure disease affection and progression, determine the Norwegian LGMD 2I prevalence, carrier frequency and genotypes, and to assess health-related quality of life in the Norwegian LGMD 2I population. Main aims are to facilitate future clinical trials and contribute to good clinical practice with suitable methodology and to complete health and social care in order to optimize the function and quality of daily living of the patient group.

Detailed description

A single-center study with Norwegian nationwide enrollment. Data is based on questionnaires, patient journals, clinical examination, a set of functional tests and biomarkers, and patient reported outcomes. Clinical/ paraclinical tests are repeated after 2-years in order to measure disease progression. Both skeletal muscle, heart and respiratory function will be examined. At baseline there will also be performed a sleep study in order to find if they are prone to sleep-disordered breathing.

Interventions

None listed

Sponsors

University of Tromso
CollaboratorOTHER
Norwegian Muscle Disease Association (FFM)
CollaboratorUNKNOWN
Norwegian National Advisory Unit on Rare Disorders (NKSD)
CollaboratorUNKNOWN
Norwegian Competence Center for Sleep Disorders
CollaboratorUNKNOWN
University Hospital of North Norway
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Genetical confirmed limb-girdle muscular dystrophy type 2I in Norway * Live in Norway * Written consent

Exclusion criteria

* Children \< 16 years are excluded from the assessment of quality of life and from the clinical/paraclinical part, but may contribute with information through questionnaires and patient journal. The study of prevalence and genotypes is anonymous and consent independent and will include everyone that is genetically LGMD 2I-confirmed in Norway.

Design outcomes

Primary

MeasureTime frameDescription
Echo intensity of musclesBaseline and 2 yearsChange in echo intensity at a defined cross-sectional level in muscles in limbs, musculus rectus abdominis and paraspinal muscles from baseline at 2 years. Echo intensity is measured as grayscale pixels ranging from 0 (black) to 255 (white) through histogram analysis by an ultrasound software program. It calculates the mean value from the superficial 1/3 of a manually selected region of interest in three consecutive images from same location. Increase in echo intensity indicates increase in pathology.
Muscle thicknessBaseline and 2 yearsUsing ultrasound to measure changes in muscle thickness at a defined cross-sectional level in muscles in limbs, musculus rectus abdominis and paraspinal muscles from baseline at 2 years.
Age at important disease stagesRetrospective data collection at baselineDocument the variation in age of onset, age of loss of walking ability, age of established cardiac failure and age of established respiratory failure.
Rate of symptom progressionRetrospective data collection at baselineDocument the variation in time from disease onset to loss of walking ability
Prevalence of recognized cardiomyopathyRetrospective data collection at baselineThe percentage of females and males with recognized cardiomyopathy
Prevalence of initiated ventilation supportRetrospective data collection at baselineThe percentage of female and males that have initiated ventilation support.
Motor task performanceBaseline and 2 yearsUsing the standardised scoring instrument Motor Function Measure for neuromuscular diseases (MFM) to measure the ability to perform 32 different motor tasks. The individual item score ranges from 0 (cannot initiate the task) to 3 (performs fully and normally). The items are divided into 3 domains: 1) Standing and transfers (13 tasks), 2) Axial and proximal motor function (12 tasks), 3) Distal motor function (7 tasks). The 3 domains give rise to 3 subscores. Both subscores and total score (0-96 points) will be measured. Baseline and changes from baseline at two years.
Disease-specific health-related quality of life (HRQOL)Baseline, at 6 months, 1 yearUsing the Individualized Neuromuscular Quality of Life (INQOL)-questionnaire to measure the burden of disease. It consists of 45 items. Each item is graded by a 7-point Likert scale (0-6/1-7).The 45 items make up 3 dimensions/domains: muscular symptoms, effects on life-domains (activities, independence, emotions, body image, social relationships) and effects of treatment. The 3 domains are together subdivided into 11 subdimensions, each with its own subscale. In addition there is a QOL-score which is a composite score from the Life-domain. The scores range from 0-100 and are determined by the item responses and a weighting algorithm. The higher the scores, the more negative impact. Both subscales and QOL-score will be determined - at baseline and changes from baseline at 6 months, 1 year and 2 years.
Echocardiography strain speckle-trackingBaseline and 2 yearsMeasure cardiac function at baseline and changes from baseline at 2 years
Nocturnal arterial carbon dioxide (CO2)-levelBaselineMonitor transcutaneous CO2 during sleep at baseline.
MRIAt 2 yearsMuscle MRI lower limbs

Secondary

MeasureTime frameDescription
Nocturnal oxygen saturationBaseline and 2 yearsMonitor transcutaneous oxygen saturation during sleep.
Cough Peak FlowBaseline and 2 yearsCough Peak Flow at baseline and changes from baseline at 2 years
Apnea-hypopnea indexBaselineUsing polysomnography to calculate the number of obstructive and non-obstructive apnea and hypopnea events pr hour sleep.
Respiratory disturbance indexBaselineUsing polysomnography to calculate the number of respiratory events in terms of apneas, hypopneas and respiratory effort-related arousals pr hour sleep.
Thoracoabdominal breathing pattern during sleepBaselineUsing polysomnography to detect paradoxal breathing movements during sleep (abdomen moving in on inspiration when supine).
Echocardiography - conventionalBaseline and 2 yearsMeasure cardiac function at baseline and changes from baseline at 2 years
Electrocardiography (ECG)Baseline and 2 yearsAssessment of cardiac electrical activity at baseline and changes from baseline at 2 years
Pain (visual analogous scale, VAS)Baseline and 2 yearsPatient-reported pain on VAS at baseline and at 2 years
6 Minute Walk Test (6MWT)Baseline (2 tests with 1 day interval) and two years (2 tests with 1 day interval)Walk distance in 6 minutes, Borgs scale for dyspnoea and fatigue pre and post test, and for self-reported exertion. Changes from baseline in 6MWT at 2 years
Fatigue Severity Scale (FSS)Baseline and 2 yearsFatigue at baseline and at 2 years
Epworth Sleepiness Scale (ESS)BaselineAssessment of daytime sleepiness at baseline
Capillary blood gasBaseline and 2 yearsCapillary CO2 at baseline and at 2 years
Serum Creatine Kinase (s-CK)Baselines-CK at baseline and at 2 years
InsomniaBaselineUsing Bergen Insomnia Scale to measure insomnia.
Sleep qualityBaselineUsing Pittsburgh Sleep Quality index to measure sleep quality
Cognitive statusBaselineMontreal Cognitive Assessment
Fatigue (Visual Analogous Scale, VAS)Baseline and 2 yearsPatient-reported fatigue on VAS tat baseline and at 2 years
4-step stair climb testBaseline and 2 yearsChanges from baseline in time to ascend and to descend a 4-steps stair at two years
Level of motor independence: Vignos GradeBaseline and 2 yearsUsing Vignos grade to score level of motor independence. The score ranges from 1 (walk and climb without assistance) to 10 (confined to bed).
Upper limb movement ability: Brooks GradeBaseline and 2 yearsUsing Brooks Grade to score the ability to raise arms above the head, ranging from 1 (normal: full abduction until the hands touch above the head) to 6 (cannot raise hands to mouth and has no useful function of hands). Baseline and changes from baseline at two years.
Hand held dynamometryBaseline and 2 yearsChanges from baseline in muscular strength in the limbs at two years
Manual Muscular Testing (MMT)Baseline and 2 yearsChanges from baseline in muscular strength in the limbs at two years
General health-related quality of lifeBaseline, 6 months, 1 yearUsing the Norwegian translation of general HRQOL-instrument Short Form Health Survey (SF-36). It is a questionnaire with 36 questions (items) investigating 8 domains/dimensions (physical function, physical role limitations, emotional role limitations, social functioning, bodily pain, general health perceptions, vitality, mental health). The 8 domain scores will be determined. The scores range from 0-100 and are based on item-responses and weighting algorithm. High score stands for good health. Measure at baseline and changes from baseline at 6 months, 1 year and 2 years.
PlethysmographyBaseline and 2 yearsLung volumes at baseline, and changes from baseline at two years.
Mean Inspiratory and Expiratory Pressure (MIP/MEP)Baseline and 2 yearsStatic respiratory pressures at baseline, and changes from baseline at two years
Forced Vital Capacity (FVC)Baseline and 2 yearsDynamic spirometry while sitting, and supine when normal sitting. Baseline and changes from baseline at 2 years
Diaphragm thickness ratioBaseline and 2 yearsUsing ultrasound to measure thickness of diaphragm at maximum inspiration and at end-expiration. Ratio \< 1,2 indicates reduced diaphragm movement. Bott left and right side will be measured.

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026