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Parent Therapist Partnership to Provide Early, Intensive Exercise in Perinatal Stroke

Parent Therapist Partnership to Provide Early, Intensive Exercise to Enhance Walking Outcomes in Children With Perinatal Stroke

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03672864
Enrollment
18
Registered
2018-09-17
Start date
2019-02-15
Completion date
2026-04-22
Last updated
2026-08-26

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

Conditions

Perinatal Stroke

Keywords

Walking, Intensive exercise, Rehabilitation, Cerebral Palsy, Early intervention

Brief summary

A prospective, single blind, parallel group, randomized control trial to determine if early, intensive lower extremity activity delivered by a physical therapist and a parent in partnership improves gross motor function more than usual care.

Detailed description

A mixed-methods randomized controlled trial at 3 healthcare centres: Edmonton, Calgary and Ottawa. The period of participation for each child is 12 months. The Immediate Group will have 3 months of intervention and 9 months follow-up. The Delay Group will be followed for 6 months (waitlist-control period), then given the opportunity to receive the same intervention and followed for 3 months after the intervention. The intervention will be delivered by clinicians in the rehabilitation centres in partnership with the child's parents. Therapists will provide training 2 days a week and will coach the parents to provide the training at home for 2 days a week. The intervention is ELEVATE (Engaging the Lower Extremity Via Active Therapy Early) and consists of child-initiated, intensive leg activities for one hour a day, four days a week for 12 weeks.

Interventions

Intensive, child-initiated movement of the lower extremity: 1 hour/day, 4 days/week, 2 sessions delivered by a physical therapist, 2 delivered by a parent. All activities are play based, and exercise intensity is enhanced by small weights placed on the dorsum of the foot and the ankle of the affected limb. Intervention is delivered over 12 weeks for a target of 48 hours of training.

Sponsors

University of Alberta
Lead SponsorOTHER
Brain Canada
CollaboratorOTHER

Study design

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

Masking description

Assessing therapists are masked to the child's group assignment.

Intervention model description

Randomized, controlled trial

Eligibility

Sex/Gender
ALL
Age
8 Months to 36 Months
Healthy volunteers
No

Inclusion criteria

* children ages 8 months to 3 years * medical history and physical exam consistent with perinatal stroke * hemiparesis in the upper and/or lower extremity * parental agreement to adhere to the training and testing schedule

Exclusion criteria

* bilateral motor impairment * epileptic seizures that could interfere with training * cognitive, behavioural or developmental impairments that preclude participation in the protocol * botulinum toxin A injections or surgery in the lower extremities within the previous six months * concurrent casting during the intervention phase (including constraint-induced movement therapy with casting) * diagnosis associated with neurological/developmental regression * parent unable to communicate (verbal and written) in English or French

Design outcomes

Primary

MeasureTime frameDescription
Gross Motor Function Measure (GMFM-66) - change from baseline3 months, 6 months, 9 months, 12 monthsA 66 item criterion referenced observational measure of gross motor skills designed for children with cerebral palsy.

Secondary

MeasureTime frameDescription
The Pediatric Quality of Life Measure module for cerebral palsy (PedsQL CP) - change from baseline3 months, 6 months, 9 months, 12 monthsA questionnaire completed by parents including 5 scales: 1) daily activities, 2) movement and balance, 3) pain and hurt, 4) fatigue, and 5) eating activities.
Ankle joint angle at onset of stretch reflex - change from baseline3 months, 6 months, 9 months, 12 monthsAnkle joint angle caused by the stretch reflex will be measured with the Portable Spasticity Assessment Device (PSAD). A hand-held segment of the device is applied to the foot segment to measure the motion of the limb. Disposable, surface electromyographic electrodes are applied to the skin of the limb to measure the muscle activity.
Ankle joint angle at full dorsiflexion - change from baseline3 months, 6 months, 9 months, 12 monthsAnkle joint angle at the extreme of dorsiflexion will be measured with the Portable Spasticity Assessment Device (PSAD). A hand-held segment of the device is applied to the foot segment to measure the motion of the limb. Disposable, surface electromyographic electrodes are applied to the skin of the limb to ensure the muscle is relaxed during the measurement.
Resource use questionnaireBaselineAll health, community, and social service use will be collected at baseline and every six months throughout the one year study period using the Resource Use Questionnaire, a tool validated for use in participants with neurodevelopmental disabilities. Costs related to lower extremity therapy as well as resources used for treatment and management of the child's cerebral palsy will be included over the study period.
Young Children's Participation and Environment Measure (YC-PEM) - change from baseline3 months, 6 months, 9 months, 12 monthsA questionnaire completed by parents to assess participation in three settings: home, daycare/preschool, and the community.

Countries

Canada

Contacts

PRINCIPAL_INVESTIGATORJaynie Yang

University of Alberta

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 27, 2026