Endermotherapy for Children With Developmental Disabilities

The Hong Kong Polytechnic University

Status and phase: Completed; Phase 2

Conditions: Cerebral Palsy; Developmental Delay

Treatments: Procedure: Passive manual stretching; Procedure: Endermotherapy

Study type: Interventional

Funder types: Other

Identifiers

NCT01207570

HSEARS20091207001

Details and patient eligibility

About

Children with developmental disabilities often sustain decreased range of motion in their extremities. The decrease in flexibility may be due to neuromuscular disorders such as spasticity or dystonia. Other causes may be imbalance in muscle strength surrounding a joint, leading to inappropriate habitual posture. Over time, muscle contracture may result for those muscle groups that are placed in a shortened position for an extended period of time. The most common site of muscle contractures among these children are gastrocnemius/soleus (lower limbs), and latissimus dorsi muscles (upper limbs). Muscle contractures can lead to further decline in functional abilities. Therefore, it is important to identify effective intervention strategies to enhance or maintain muscle flexibility in children with developmental dysfunctions.

Commercially available endermotherapy device has been used to soften scar tissue following burn injuries. The mechanical stimulation applied may also have beneficial effects on relaxing the muscle tissue. The overall aim of the proposed study is to determine whether endermotherapy treatment has immediate effect in improving joint range of motion among children with developmental disabilities.

The research hypothesis is that children in the endermotherapy group will have significantly more gain in ankle passive range of motion than those in the control group.

Enrollment: 54 patients

Sex: All

Ages: 2 to 6 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• children aged between 2 and 6.
• children with diagnosis of cerebral palsy or developmental disabilities.
• Has limited ankle dorsiflexion range of motion (less than 20 degrees)

Exclusion criteria

• Other serious illnesses that preclude participation

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: Single Blind

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54 participants in 2 patient groups

Endermotherapy

Experimental group

Description:

The subjects in the experimental group will receive a single session (5 minutes) of endermotherapy) applied to the gastrocnemius/soleus muscle group in the more affected side. The treatment will b e carried out by a qualified physiotherapist.

Treatment:

Procedure: Endermotherapy

Passive stretching

Active Comparator group

Description:

The subjects in this group will receive a single session of passive stretching of the gastrocnemius/soleus muscle for 5 minutes.

Treatment:

Procedure: Passive manual stretching