Effectiveness of Family Collaborative Physiotherapy Programs With High-risk Infants
NCT ID: NCT04035291
Last Updated: 2021-04-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
63 participants
INTERVENTIONAL
2019-08-01
2020-07-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
TRIPLE
Study Groups
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Interventional
The first group (n = 25) will be asked to apply the physiotherapy program by the family at home that includes the principles of therapeutic handling-holding-positioning of NDT principles, starting at the third month for 8 weeks. And It will last for at least 45 minutes, 3 days a week. Family education will be evaluated after 4 weeks and improvements will be made in accordance with the motor development of the infant. The program will be implemented by families for 8 weeks.
exercise
exercises,play therapy models and positioning, handling and holding principles for babies, daily routins
Experimental
In the second study group (n = 25), family collaborative physiotherapy program will be applied by the family. This program will start from the postterm third month, and will include family trainings based on the goal-oriented active motor learning model of the baby in an 8-week in enriched environment and to include holding-carrying-positioning trainings in daily routines. Also it will last for at least 45 minutes, 7 days a week. All members of the family will be included in the family trainings and home visits will be made at 2-week intervals. Families will be encouraged to apply the physiotherapy processes of their babies in their natural environment at every moment of their daily routines (feeding, carrying on lap, gas extraction, changing the bed, sleeping, waking time, shopping moment, playing games etc.).
exercise
exercises,play therapy models and positioning, handling and holding principles for babies, daily routins
control
In the third study group, families who are out of town or who cannot participate in the treatment program for other reasons will be included in the evaluations.
No interventions assigned to this group
Interventions
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exercise
exercises,play therapy models and positioning, handling and holding principles for babies, daily routins
Eligibility Criteria
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Inclusion Criteria
* Chronic pulmonary disease Infants with dysplasia and long-term O₂ support
* Preterm infants with sepsis, necrotizing enterocolitis (NEC), infantile apnea, cerebral malformation due to gram negative bacteria
* Patients with a low Apgar score of 5 minutes (3 and less), multiple births (twins, triplets) diagnosed with intrauterine growth retardation, preterm infants with premature retinopathy (ROP)
* Infants with prolonged severe hypoglycemia and hypocalcemia
* Surgical conditions such as diaphragmatic hernia or tracheoesophageal fistula
* Infants younger than gestational age (Small for Gestational Age, SGA, smaller than 3rd percentile) or older than gestational age (Large for Gestational Age, LGA, greater than 97th percentile)
* Babies receiving mechanical ventilation for more than 24 hours
* Babies less than 32 weeks of gestation and born under 1500 g
Exclusion Criteria
* Infants diagnosed with metabolic and genetic diseases (Down Syndrome, Spinal Muscular Atrophy, Duchenne Muscular Dystrophy etc.)
* Infants still intubated and mechanical ventilator dependent at postterm 3 months
24 Weeks
40 Weeks
ALL
No
Sponsors
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Sanko University
OTHER
Responsible Party
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Hatice Adıgüzel
Principal Investigator
Principal Investigators
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Hatice Adıgüzel, PhD cd.
Role: PRINCIPAL_INVESTIGATOR
Sanko University
Locations
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Sanko University
Gaziantep, Şehitkamil, Turkey (Türkiye)
Countries
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Other Identifiers
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Sanko U
Identifier Type: -
Identifier Source: org_study_id
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