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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.

3 listopada 2026 zaktualizowane przez: Prof. Dr. Shoaib Waqas, Lahore University of Biological and Applied Sciences

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.

Przegląd badań

Status

Rekrutacyjny

Warunki

Interwencja / Leczenie

Szczegółowy opis

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.

Typ studiów

Interwencyjne

Zapisy (Szacowany)

44

Faza

  • Nie dotyczy

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Kontakt w sprawie studiów

Lokalizacje studiów

    • Punjab Province
      • Lahore, Punjab Province, Pakistan
        • Rekrutacyjny
        • Ghurki Trust and Teaching Hospital

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

3 lata do 7 lat (Dziecko)

Akceptuje zdrowych ochotników

Nie

Płeć kwalifikująca się do nauki

Wszystko

Opis

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:

  • 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.

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Leczenie
  • Przydział: Randomizowane
  • Model interwencyjny: Przydział równoległy
  • Maskowanie: Pojedynczy

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Eksperymentalny: 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.

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.

Aktywny komparator: 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.

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.

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Gross motor function (Gross Motor Function Measure-88)
Ramy czasowe: Baseline (Week 0) and post-intervention (Week 6).

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.

Baseline (Week 0) and post-intervention (Week 6).
Functional independence (Pediatric Functional Independence Measure)
Ramy czasowe: Baseline (Week 0) and post-intervention (Week 6).

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.

Baseline (Week 0) and post-intervention (Week 6).
Balance (Pediatric Balance Scale)
Ramy czasowe: Baseline (Week 0) and post-intervention (Week 6).

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.

Baseline (Week 0) and post-intervention (Week 6).
Health-related quality of life (Pediatric Quality of Life Inventory)
Ramy czasowe: Baseline (Week 0) and post-intervention (Week 6).

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.

Baseline (Week 0) and post-intervention (Week 6).

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Sponsor

Śledczy

  • Dyrektor Studium: Dr. Shoaib Waqas, PHD, Lahore University of Biological and Applied Sciences

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Rzeczywisty)

12 października 2026

Zakończenie podstawowe (Szacowany)

30 grudnia 2026

Ukończenie studiów (Szacowany)

1 stycznia 2027

Daty rejestracji na studia

Pierwszy przesłany

3 listopada 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

3 listopada 2026

Pierwszy wysłany (Rzeczywisty)

9 listopada 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

9 listopada 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

3 listopada 2026

Ostatnia weryfikacja

1 listopada 2026

Więcej informacji

Terminy związane z tym badaniem

Inne numery identyfikacyjne badania

  • UBAS/ERB/26/07/084

Plan dla danych uczestnika indywidualnego (IPD)

Planujesz udostępniać dane poszczególnych uczestników (IPD)?

NIE

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt leczniczy regulowany przez amerykańską FDA

Nie

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .