Title

Effect of a Nutritional Support System for Improving Gross Motor Function in Cerebral Palsy
CONTROLLED, RANDOMIZED, BLIND CLINICAL TRIAL OF EFFECT OF A NUTRITIONAL SUPPORT SYSTEM (DIET, SUPPLEMENTS AND PROBIOTIC) FOR IMPROVING GROSS MOTOR FUNCTION IN CEREBRAL PALSY
  • Phase

    N/A
  • Study Type

    Interventional
  • Status

    Completed No Results Posted
  • Intervention/Treatment

    deworming ...
  • Study Participants

    30
Background: Most patients with cerebral palsy (CP) are dependent on parents due to the spasticity and limitations in their gross motor function. Additionally, many of them do not respond to physical therapy due to deterioration in their nutritional status, which is secondary to gastrointestinal disorders, parasitosis, dysbiosis and the catabolic state of the disease itself. Evidence suggests that greater independence and better clinical response can be achieved by correcting the nutritional status. However, basic treatments only contemplate the calculation of energy requirements and do not consider important nutrients in particular, supplementation with glutamine, arginine, zinc, selenium, colecalciferol, nicotinic acid, spirulina, omega 3, ascorbic acid, vegetal protein or even probiotics.

Objective: To determine the effect of using a nutritional support system (NSS) diet, supplements and probiotic on the gross motor function in children with CP with spastic diparesic and Gross Motor Function Classification System III (GMFCS III).

Material and methods: In an exploratory study with controlled clinical trial design, 30 patients were randomly assigned to receive: 1) dietary surveillance and conventional therapy (FG), 2) deworming and WHO diet (CG), or 3) deworming and the NSS (IG). The patients were recruited from the Children´s Telethon Rehabilitation Center (CRIT) in Tlalnepantla Estado de México. Males and females aged 4-12 years were included with CP and spastic diparesic GMFCS III, who had a full-time caregiver and whose parents agreed to participate. They were studied for thirteen weeks. Gross motor function was evaluated at baseline and at 7 and 13 weeks after therapy using the GMFM scale.
Study Started
Jan 12
2015
Primary Completion
Dec 18
2015
Study Completion
Apr 07
2017
Last Update
May 01
2019

Dietary Supplement Nutritional Support System (NSS)

Envelope 1 4.9g of Spirulina, 100mg ascorbic acid, 5mg folic acid and 10mg of glutamine. Was to be added to shake 1 during the first 10 days. Envelope 2 1g PUFAs n-3 and was to be added to shake 2 which was given throughout the intervention. Envelope 3 4.9g of Spirulina Maximum, 100mg ascorbic acid, 5mg folic acid, 5.2g vegetable protein, 125mg nicotinic acid, 50mg zinc, 100 mcg selenium and 800 UI cholecalciferol. Was to be added to shake 1 from day 11 until the end of week 6, after which it was suspended for 10 days and substituted for envelope 5 and then to be retaken until the end of the intervention. Envelope 4. 1g arginine and was to be added to shake 3 from day 8 until the end of the intervention. Envelope 5 contained the same ingredients as envelope 3 with an additional 10mg glutamine and was to be added to shake 1 from the start of week 7 for 10 days, after which envelope 3 was restarted. Probiotic at a dosage of 200 mg every 12 hours for 3 days at the beginning and week 6

  • Other names: Intervention treatment

Other deworming

nitazoxanide at a dosage of 7.5 mg / kg every 12 hours for 3 days.

Other recommended diet

WHO Diet

Follow-up Group (FG) No Intervention

dietary surveillance and conventional therapy

Control Group (CG) Active Comparator

deworming and WHO diet

Intervention Group (IG) Experimental

deworming and the Nutritional Support System (NSS)

Criteria

Inclusion Criteria:

Patients with CP with spastic diparesia and GMFCS III
Re-entry
Presence and support of a full-time caregiver
To tolerate oral feeding
Parents or guardians agree in writing to participate in the project
Patients treated at the CRIT of Tlalnepantla Edo. Mex
That the children, in the case of being able to write, accept in writing to participate in the project

Exclusion Criteria:

Presence of any other catabolic disease, which further increases the risk of malnutrition (renal, cardiovascular, pulmonary, hepatic, immunological)
Have had infectious problems or have received antibiotic treatment 15 days prior to the start of the study.
Have received botulinum toxin therapy in the last 4 months
Muscle relaxants in the last 6 months
Severe gastroesophageal reflux
Patients with any type of surgery performed with a period shorter than 9 months
That can walk by themselves
No Results Posted