Working… Menu

Investigation Of Factors Affecting Hand Functions in Nonambulatory Patients With Duchenne Muscular Dystrophy

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT03521271
Recruitment Status : Completed
First Posted : May 10, 2018
Last Update Posted : May 10, 2018
Information provided by (Responsible Party):
Gülcan Altınok, Hacettepe University

Brief Summary:
The aim of this study, determining the factors affecting the hand functions of children with Duchenne Muscular Dystrophy who have lost their independent ambulatory ability and determining the effects on the overall upper extremity performance and quality of life of the determined factors.

Condition or disease
Duchenne Muscular Dystrophy

Detailed Description:

Duchenne Muscular Dystrophy (DMD) is the most common neuromuscular disease seen in childhood. DMD is an X linked recessive disorder. DMD is characterized by complete or partial (<3%) deficiency of the cell membrane protein dystrophin.

Dystrophin deficiency results in a permanent deterioration of muscle fibers. This leads to a progressive decrease in muscle strength and functional abilities. The precise mechanism of how the defect of dystrophin leads to degeneration of muscle fibers remains uncertain, but cytoskeletal deterioration, sarcolemmal instability and abnormal calcium homeostasis are thought to play a role in this degeneration.

These patients have symptoms such as limb proximals and progressive muscle weakness in the trunk, gait abnormalities, Gower's sign, various degrees of restriction in daily living activities, and frequent falls. The majority of patients have elevated serum creatine kinase or elevated liver transaminases and less frequently language or general developmental retardation.

Walking ability of this children begins to deteriorate between the ages of 3-6. These patients are generally dependent on wheelchair aged 10-12 years. The loss of walking is the milestone in terms of the progression of the disease. The use of electric wheelchairs limits arm functions such as lengthening and lifting during the late phase of the illness (when the ambulance has been lost and the ambulance is being continued with the wheelchair).

Patients with DMD have an average life span of 30 years with spinal surgery and ventilation support. They spend most of their lives dependent on the wheelchair and need functional use of the upper limbs to maintain the best possible level of independence in their daily life activities throughout their lifetimes.

Although muscle weakness in the proximal limbs is the first finding of the disease, the influence of upper extremity functions gives symptoms after 8 years of age and has a great influence on the level of independence of DMD patients in life since this process. For this reason, rehabilitation approaches for the protection of upper extremity functions from the early period of the disease are of great importance.Effective interventions are necessary to achieve this goal and these variables must be considered when making clinical decisions.

Patients with adult DMD have been shown to be able to perform important functional activities with limited distal motor function in the late phase of disease, but tend to lose these capacities as muscle strength decreases. For this reason, determining the factors (grip strength, thumb opposition, upper extremity joint range of motion, upper extremity muscle strength, etc.) that may affect hand functions, which is an important component in maintaining upper extremity functioning, and how these factors are related to the general functions of the upper extremity it is crucial that this disease leads to physiotherapy rehabilitation programs to be implemented.

Layout table for study information
Study Type : Observational
Actual Enrollment : 23 participants
Observational Model: Case-Only
Time Perspective: Prospective
Official Title: Investigation Of Factors Affecting Hand Functions in Nonambulatory Patients With Duchenne Muscular Dystrophy
Actual Study Start Date : April 5, 2017
Actual Primary Completion Date : January 26, 2018
Actual Study Completion Date : January 26, 2018

Primary Outcome Measures :
  1. Brooke Upper Extremity Functional Classification (1-6) [ Time Frame: 2 minutes ]

    Children's functional levels were assessed with Brooke Upper Extremity Functional Classification (BUEFS) and children with a BUEFS score between 1-5 were included in the study.

    1. Starting with arms at sides, can abduct arms in a full circle until they touch above head
    2. Can raise arms above head only by flexing elbow or using accesory muscles
    3. Cannot raise arms above head but can raise a glass of water to mouth (using both hands if necessary)
    4. Can raise hands to mouth but cannot raise a glass of water to mouth
    5. Cannot raise hand to mouth but can use hands to hold pen or pick up pennies from table
    6. Cannot raise hands to mouth and has no useful function of hands

  2. Passive joint range of motion [ Time Frame: 10 minutes ]
    Passive range of motions were assessed with goniometer and recorded limitations.

  3. Upper extremity muscle strength [ Time Frame: 20 minutes ]
    Hand held dynamometer

  4. Thumb opposition [ Time Frame: 2 minutes ]

    Thumb opposition was assessed by Kapandji score (1-10). Score Location achieved

    1. Radial side of the proximal phalanx of the 2nd phalanx
    2. Radial side of the middle phalanx of the 2nd phalanx
    3. Tip of the 2nd phalanx
    4. Tip of the 3th phalanx
    5. Tip of the 4th phalanx
    6. Tip of the 5th phalanx
    7. Distal interphalangeal joint crease of the 5th phalanx
    8. Proximal interphalangeal joint crease of the 5th phalanx
    9. Metacarpophalangeal joint crease of the 5th phalanx
    10. Distal palmar crease

  5. Lateral, tripod, two-point pinch strength [ Time Frame: 3 minutes ]

  6. Performance of the upper extremity [ Time Frame: 15 minutes ]

    Performance of the Upper Limb (PUL) (0-74) is including three dimension:

    • Shoulder dimension (0-16)
    • Elbow dimension (0-34)
    • Distal dimension (0-24)

  7. Hand function [ Time Frame: 3 minutes ]
    ABILHAND-Kids (0-36)

  8. Activity limitations [ Time Frame: 3 minutes ]
    ACTIVLIM (0-36)

  9. Gross grip strength [ Time Frame: 2 minutes ]
    Hand dynamometer

Secondary Outcome Measures :
  1. Quality of life assessment of children (0-100) [ Time Frame: 5 minutes ]
    PedsQL-Child report

  2. Quality of life assessment of parents (0-100) [ Time Frame: 5 minutes ]
    PedsQL-Parent report

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

Layout table for eligibility information
Ages Eligible for Study:   8 Years to 16 Years   (Child)
Sexes Eligible for Study:   Male
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients who applied to the Pediatric Neuromuscular Diseases Unıt of Hacettepe University Physiotherapy and Rehabilitation Department

Inclusion Criteria:

  • Having a Duchenne Muscular Dystrophy diagnosis by a practicing physician,
  • Between the ages of 8-16 years,
  • Having lost ambulation ability,
  • Brooke Upper Extremity Functional Classification (1-5)
  • To have motivation and co-operation with physiotherapist for evaluations to be made

Exclusion Criteria:

  • To maintain the capacity of independent ambulance,
  • Having cooperative disorder or serious mental disorder,
  • Any spinal and / or upper extremity injuries and / or surgery in the last 6 months,
  • Having any systemic disease other than DMD,
  • Not volunteering to participate in the study

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT03521271

Layout table for location information
Hacettepe University
Ankara, Samanpazarı/Ankara, Turkey, 06100
Sponsors and Collaborators
Hacettepe University

Layout table for additonal information
Responsible Party: Gülcan Altınok, Master Student, Hacettepe University Identifier: NCT03521271     History of Changes
Other Study ID Numbers: GO 17/307
First Posted: May 10, 2018    Key Record Dates
Last Update Posted: May 10, 2018
Last Verified: May 2018
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Undecided

Layout table for additional information
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Gülcan Altınok, Hacettepe University:
Duchenne Muscular Dystrophy
Upper limb
Hand functions
Grip Strength
Additional relevant MeSH terms:
Layout table for MeSH terms
Muscular Dystrophies
Muscular Dystrophy, Duchenne
Muscular Disorders, Atrophic
Muscular Diseases
Musculoskeletal Diseases
Neuromuscular Diseases
Nervous System Diseases
Genetic Diseases, Inborn
Genetic Diseases, X-Linked