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RecruitingNCT07924813Updated Nov 9, 2026

Effects of Functional Electrical Stimulation Combined With Task-Oriented Training on Lower Limb Function, Balance, and Quality of Life in Children With Spastic Diplegic Cerebral Palsy.

An interventional study of Functional Electrical Stimulation Combined with Task- Oriented Training (FES+TOT) and Task-Oriented Training (TOT) in Diplegic Spastic Cerebral Palsy, sponsored by Lahore University of Biological and Applied Sciences. Recruiting at 1 site in Pakistan. Open to participants aged 3 Years to 7 Years. Per ClinicalTrials.gov, last updated 2026-11-09.

Sponsored by Lahore University of Biological and Applied Sciences · Not applicable, Interventional, and Treatment

Updated Nov 9, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
44
Allocation
Randomized
Ages
3 Years to 7 Years
Sex
All
01

Study summary

This study aims to compare the effects of Functional Electrical Stimulation (FES) combined with Task-Oriented Training (TOT) and Task-Oriented Training alone on gross motor function, balance, and quality of life in children with spastic diplegic cerebral palsy. Children with this condition commonly experience lower-limb weakness, increased muscle tone, impaired balance, and difficulties with standing and walking.

A total of 44 children aged 3-7 years will be recruited. Participants will be randomly allocated into two groups: the experimental group will receive FES combined with task-oriented training, while the control group will receive task-oriented training alone. Both groups will undergo supervised treatment three times per week for six weeks, with each session lasting 60 minutes.

The experimental group will receive FES applied to the gluteus medius muscle alongside task-oriented training. Task-oriented training will include sit-to-stand practice, standing balance, walking, stepping, obstacle negotiation, and stair training. Outcomes will be assessed before and after the intervention using the Gross Motor Function Measure (GMFM), Pediatric Balance Scale (PBS), Pediatric Functional Independence Measure (WeeFIM), and Pediatric Quality of Life Inventory (PedsQL). The study aims to determine whether combining FES with task-oriented training leads to greater improvements in gross motor function, balance, and quality of life.

Read the detailed description

Spastic diplegic cerebral palsy is a subtype of cerebral palsy characterized by predominantly lower-limb involvement, often resulting in increased muscle tone, muscle weakness, impaired selective motor control, and difficulties with standing, walking, balance, and functional mobility. These impairments can restrict children's participation in daily activities and negatively affect their functional independence and quality of life. Routine physiotherapy is commonly used to address these limitations; however, improvements in basic motor performance may not always translate into better performance of functional activities requiring coordinated movement, postural stability, and dynamic balance. Therefore, rehabilitation approaches that combine targeted muscle activation with repetitive, goal-directed functional practice may offer additional benefits for children with spastic diplegic cerebral palsy.

Functional Electrical Stimulation (FES) uses controlled electrical impulses to stimulate peripheral motor nerves and produce muscle contraction. When appropriately applied during functional activities, FES may facilitate muscle activation and support movement performance. Task-Oriented Training (TOT) is a rehabilitation approach based on repetitive practice of meaningful, goal-directed activities designed to improve motor learning, functional performance, and the transfer of acquired skills into everyday activities. Combining FES with TOT may provide additional benefits by facilitating targeted muscle activation while children practice functional movements. However, evidence regarding the combined effects of FES and task-oriented training on lower-limb function, balance, and quality of life in young children with spastic diplegic cerebral palsy remains limited. This study is designed to address this gap by comparing the effects of FES combined with TOT and TOT alone.

This study will be conducted as a two-arm, parallel-group randomized clinical trial involving 44 children aged 3-7 years with spastic cerebral palsy who meet the predefined eligibility criteria. Participants will be randomly allocated to either the experimental group or the control group in a 1:1 ratio. A computer-generated randomization sequence will be prepared by an independent researcher who will not be involved in participant recruitment, treatment, or outcome assessment. Allocation concealment will be maintained using sequentially numbered, opaque, sealed envelopes. Participants will undergo a six-week intervention program consisting of three supervised sessions per week, with each session lasting 60 minutes. The experimental group will receive Functional Electrical Stimulation combined with Task-Oriented Training, while the control group will receive Task-Oriented Training alone. The FES intervention will target the gluteus medius muscle to facilitate muscle activation during standing and functional movement activities. Electrical stimulation will be delivered using a frequency of 35 Hz, a pulse width of 250 microseconds, a ramp time of 1-2 seconds, and an on-to-off ratio of 1:3. Stimulation intensity will be adjusted according to the child's tolerance to achieve visible and comfortable muscle contractions.

Task-Oriented Training will involve progressive, structured practice of functional activities selected to address standing control, weight shifting, stepping, walking, dynamic balance, and functional mobility. During the first week, training will focus on sit-to-stand transitions, standing weight shifts in side-to-side and forward-backward directions, and level-surface walking. During the second week, activities will progress to overground walking, step initiation, and forward and lateral stepping. The third week will include obstacle crossing, stepping over floor markers, and multidirectional stepping to challenge dynamic balance and movement coordination. During the fourth week, participants will practice step-ups, stair negotiation, and tandem walking. The fifth week will incorporate changes in walking direction, variations in walking speed, and dual-task walking activities. During the sixth week, training will progress to advanced gait activities, obstacle negotiation, and simulated community mobility tasks according to each child's functional ability and tolerance.

The primary outcome will be gross motor function, assessed using the Gross Motor Function Measure (GMFM-88), with particular consideration of standing and walking-related abilities. Secondary outcomes will include balance, functional independence, and health-related quality of life. Balance will be evaluated using the Pediatric Balance Scale (PBS), functional independence using the Pediatric Functional Independence Measure (WeeFIM), and health-related quality of life using the Pediatric Quality of Life Inventory (PedsQL). These outcome measures will be used to determine whether combining FES with task-oriented training produces greater improvements than task-oriented training alone.

Outcome assessments will be conducted at baseline (Week 0) before the intervention begins and immediately after completion of the six-week intervention program (Week 6). Changes in gross motor function, balance, functional independence, and quality of life will be evaluated within and between the two groups to determine the effectiveness of the interventions.

The findings of this study may provide evidence regarding the effectiveness of combining Functional Electrical Stimulation with Task-Oriented Training in improving lower-limb function, balance, functional independence, and quality of life in children with spastic diplegic cerebral palsy.

02

Conditions studied

  • Diplegic Spastic Cerebral Palsy

Keywords

  • Spastic Diplegic Cerebral Palsy, Functional Electrical Stimulation, Task-Oriented Training, Balance, Quality of Life
03

In context

Cerebral palsy, spastic, diplegic

27 studies on the registry are indexed under Cerebral palsy, spastic, diplegic; 7 are open to participants now.

This study's planned enrollment of 44 is close to the median of 42 across 23 interventional studies indexed under Cerebral palsy, spastic, diplegic.

Browse Cerebral palsy, spastic, diplegic studies →

Lead sponsor

Lahore University of Biological and Applied Sciences is the lead sponsor of 79 studies on the registry; 55 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
3 Years to 7 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Children of either gender, aged 3-7 years, diagnosed with spastic cerebral palsy - Gross Motor Function Classification System (GMFCS) Levels II and III
  • Ability to understand and follow simple verbal instructions with or without auditory device

Exclusion criteria

Exclusion Criteria:

  • Botulinum toxin injection to the lower limbs within the previous 6 months .
  • Severe fixed contractures or musculoskeletal deformities affecting gait .
  • Uncontrolled epilepsy or other neurological disorders besides cerebral palsy .
  • Cardiac pacemakers or other implanted electrical devices contraindicating FES use.
  • Severe visual, auditory, or cognitive impairments preventing participation.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
44 participants (estimated)

Study arms

  • Experimental
    Functional Electrical Stimulation + Task-Oriented Training

    Group A will receive Functional Electrical Stimulation (FES) combined with Task-Oriented Training (TOT) for six weeks. FES will be applied to the gluteus medius muscle during functional activities to facilitate muscle activation. Participants will also perform progressive task-oriented activities, including sit-to-stand practice, standing weight shifts, walking, stepping, obstacle negotiation, and stair training. Sessions will be delivered three times per week for six weeks, with each session lasting 60 minutes.

    Behavioral: Functional Electrical Stimulation Combined with Task- Oriented Training (FES+TOT)

  • Active comparator
    Task- Oriented Training

    Group B will receive routine physical therapy along with Task-Oriented Training (TOT) for six weeks. Participants will practice progressive functional activities designed to improve gross motor function, balance, and functional mobility. Training will include sit-to-stand practice, standing weight shifts, overground walking, forward and lateral stepping, obstacle crossing, step-ups, stair negotiation, changes in walking direction, and advanced gait activities. Sessions will be delivered three times per week for six weeks, with each session lasting 60 minutes.

    Behavioral: Task-Oriented Training (TOT)

Interventions

  • BehavioralFunctional Electrical Stimulation Combined with Task- Oriented Training (FES+TOT)

    Participants will receive Functional Electrical Stimulation combined with Task-Oriented Training for six weeks, with three supervised sessions per week (18 sessions in total, 60 minutes each). FES will be applied to the gluteus medius, Hamstring, quadriceps muscle using a frequency of 35 Hz, a pulse width of 250 μs, a ramp time of 1-2 seconds, and an on-to-off ratio of 1:3. Stimulation intensity will be adjusted to produce a visible, comfortable muscle contraction. Task-oriented training will include progressive functional activities such as sit-to-stand practice, standing weight shifting, level walking, stepping, obstacle negotiation, step-ups, stair training, and advanced gait activities.

  • BehavioralTask-Oriented Training (TOT)

    Participants will receive Task-Oriented Training for six weeks, with three supervised sessions per week (18 sessions in total, 60 minutes each). Training will involve progressive, goal-directed functional activities to improve gross motor function, balance, and functional mobility. Activities will progress from sit-to-stand practice, standing weight shifting, and level walking to multidirectional stepping, obstacle crossing, step-ups, stair negotiation, changes in walking direction, variations in walking speed, and advanced gait activities according to participants' abilities.

06

What researchers measure

Primary outcomes

  1. Gross motor function (Gross Motor Function Measure-88)

    The Gross Motor Function Measure (GMFM-88) is a standardized observational assessment used to evaluate gross motor function in children with cerebral palsy. This study will focus on Dimension D (Standing) and Dimension E (Walking, Running, and Jumping). Scores range from 0% to 100%, with higher scores indicating better gross motor function.

    Time frame: Baseline (Week 0) and post-intervention (Week 6).

  2. Functional independence (Pediatric Functional Independence Measure)

    The Pediatric Functional Independence Measure (WeeFIM) assesses a child's level of independence in self-care, mobility, and cognition. Total scores range from 18 to 126, with higher scores indicating greater functional independence.

    Time frame: Baseline (Week 0) and post-intervention (Week 6).

  3. Balance (Pediatric Balance Scale)

    The Pediatric Balance Scale (PBS) assesses functional balance during everyday activities in children. Total scores range from 0 to 56, with higher scores indicating better balance performance.

    Time frame: Baseline (Week 0) and post-intervention (Week 6).

  4. Health-related quality of life (Pediatric Quality of Life Inventory)

    The Pediatric Quality of Life Inventory (PedsQL) evaluates health-related quality of life across physical, emotional, social, and school functioning domains. Scores range from 0 to 100, with higher scores indicating better quality of life.

    Time frame: Baseline (Week 0) and post-intervention (Week 6).

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Oct 2026 (actual). Primary completion is estimated for Dec 2026, 2 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Nov 3, 2026
First posted
Nov 9, 2026
StartActual
Oct 12, 2026
Primary completionEst.
Dec 30, 2026
CompletionEst.
Jan 2027
Last update
Nov 9, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Nov 9, 2026
Show all 1 update
  1. Nov 9, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07924813
Lead sponsor
Lahore University of Biological and Applied Sciences
Responsible party
Prof. Dr. Shoaib Waqas (Professor, Lahore University of Biological and Applied Sciences) — Principal investigator
First posted
Nov 9, 2026
Start date
Oct 12, 2026
Primary completion
Dec 30, 2026 (estimated)
Completion
Jan 2027 (estimated)
Last update
Nov 9, 2026

Study contacts

Dr. Shoaib Waqas, PHD
Contact
shoaib.waqas@ubas.edu.pk
+92 302 4552109
Dr. Shoaib Waqas, PHD
study director · Lahore University of Biological and Applied Sciences

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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