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Blood-flow Restricted Exercise in Inclusion Body Myositis

Low-intensity Blood-flow Restricted Muscle Exercise in Patients With Sporadic Inclusion Body Myositis: a Randomised Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02317094
Enrollment
22
Registered
2014-12-15
Start date
2015-01-31
Completion date
2015-09-30
Last updated
2015-10-20

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

Conditions

Sporadic Inclusion Body Myositis

Brief summary

This study evaluates the effects of a low-intensity blood-flow restricted exerciser protocol on patient reported physical function, in patients with sporadic inclusion body myositis. The study is designed as a parallel group randomized controlled trial with a treatment group and a control group.

Detailed description

Sporadic inclusion body myositis (sIBM) is a disease characterized by skeletal muscle inflammation and severe muscle atrophy especially in the muscles in the thigh and the finger flexors. In time the muscle weakness will cause the affected person to become unable to walk and carry out basic tasks in the every day life. Currently no effective treatment exist for sIBM patients, however several studies indicate that exercise may be beneficial for the patients. In the resent years a lot of research attention has been directed toward low-intensity training with partial vascular occlusion as an alternative to the conventional high intensity strength training. Interestingly the low-intensity blood-flow occluded training is found to be at least as beneficial in causing muscle growth as the conventional strength training but with very little mechanical load on joints and tendons. Furthermore the blood-flow occluded training seem to result in a hyper-activation of muscle stem cells which play an important role in muscle regeneration. This make the blood-flow restricted training modality a very interesting treatment possibility for sIBM patients because it might be able to restore and/or maintain the skeletal muscle tissue and therefore also muscle function.

Interventions

OTHERBlood-flow restricted training

The intervention consists of low-intensity blood-flow restricted training involving 5 lower extremity exercises performed uni lateral in four sets to concentric failure with an intensity of approximately 25 repetition maximum (25RM).

DRUGCare as usual

The intervention consists of various DMARDs, which are given to the patients depending on their physical state and the disease activity.

Sponsors

Odense University Hospital
CollaboratorOTHER
University of Southern Denmark
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
35 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Clinical features * Duration of weakness \> 12 months * Weakness of finger flexors \> shoulder abductors AND knee extension \> hip flexion Pathologic features * Invasion of nonnecrotic fibres of mononuclear cells or rimmed vacuoles or * increased major histocompatibility complex I (MHC-1) but no intracellular amyloid deposits or 15-18nm filaments

Exclusion criteria

* Lack of gait function * Co-morbidity contraindicating the use of blood-flow restricted training (previous deep vein thrombosis/pulmonary embolism or known peripheral ischemic disease). * Co-morbidity preventing resistance training (severe heart/lung-disease, uncontrolled hypertension (systolic \> 160mmHg, diastolic \> 100mmHg), severe knee/hip arthritis)

Design outcomes

Primary

MeasureTime frameDescription
Patient reported physical function (health survey (SF-36) subscale: Physical Function)12 wksPatient reported physical function will be evaluated with the short form (36) health survey (SF-36) subscale: Physical Function. The scale ranges from 0 to 100 where 100 is the highest score.

Secondary

MeasureTime frameDescription
Physician/Patient Global activity (VAS scale)12 wksA VAS scale used by both physician and patient to evaluate the overall activity of the disease
Physician/Patient Global Damage (VAS scale)12 wksA VAS scale used by both physician and patient to evaluate the overall damage caused by the disease.
2-min walk test12 wksA 2-min maximal walk test where the participant is encouraged to cover the greatest distance possible.
Manual Muscle Testing (MMT)12 wksA test of muscle strength in a series of muscles, carried out by the physician
Chair rise12 wksParticipants are instructed to stand up and sit down on a chair as many times as possible in 30 sec.
Timed up & go12 wksParticipants are instructed to rise from a chair walk 3 m forward, pass a marking and return to the chair and sit down as fast as possible
Health assessment questionnaire (HAQ)12 wksHAQ is a questionnaire to evaluate patient reported disability. It has 8 categories with a range of questions. Each question is scored from 0 to 3 where 0 is no disability and 3 is unable to do.
Inclusion body myositis functional rating scale (IBMFRS)12 wksA disease specific questionnaire evaluating the patients self reported everyday function.
Myositis Disease Activity Assessment Tool (MDAAT)12 wksAn assessment tool used by the physician to evaluate disease activity in various organ systems via a scoring system and VAS scales.
Myositis Damage Index12 wksAn assessment tool used by the physician to evaluate the damage caused by the disease or co-morbid conditions, to various organ systems. The system uses VAS scales.

Other

MeasureTime frameDescription
Sway - Postural Balance (using force plate)12 wksA test of postural balance
Maximal isometric and dynamic knee extension muscle strength (Kin-Com dynamometer)12 wksThe maximal isometric and dynamic knee extension muscle strength will be evaluated in a Kin-Com dynamometer. Isometric strength data will be analyzed for peak torque, maximal impulse and maximal contractile rate of force development (RFD)
Leg extension muscle power (Nottingham Power Rig)12 wksThe Nottingham Power Rig is used for evaluating the maximal muscle power that can be generated in the leg extensors.
Central activation (assessed with the twitch interpolation technique)12 wksVoluntary muscle activation will be assessed with the twitch interpolation technique.
Body composition ( full body duel energy X-ray absorption scan)12 wksBody composition will be evaluated with a full body duel energy X-ray absorption scan.
Blood samples12 wksBlood samples will be drawn for storage in a bio bank, for future analysis.
Muscle biopsies12 wksMuscle biopsies will be taken on a selected number of subjects from either the vastus lateralis or the tibialis anterior muscle, for the use in future analysis of i.e. muscle fibre size and distribution, myogenic stem cell activity, capillary density, muscle inflammation ect.

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 14, 2026