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Early Intervention for Developmental Delay

Chang Gung Medical Foundation logo

Chang Gung Medical Foundation

Status

Completed

Conditions

Child Development
Developmental Delay
Early Intervention

Treatments

Behavioral: OPD+SI intervention program
Behavioral: Day-Care early intervention program
Behavioral: OPD intervention program

Study type

Interventional

Funder types

Other

Identifiers

NCT03223688
105-1742C1

Details and patient eligibility

About

This study aims to investigate the effectiveness of early intervention program in Department of Children and Adolescent Psychiatry, Kaohsiung Chang Gung Memorial Hospital. The investigators assume that the frequency of early-intervention and degree of family involvement will be associate with the treatment outcome.

Full description

This prospective, non-randomized, open-label study is performed to assess the effects of adjunctive SI in the family-based treatment program of children with developmental delay (DD). The study subjects are children with DD who attended an early intervention (EI) program at Kaohsiung Chang Gung Memorial Hospital, which is the largest general hospital in the Southern Taiwan. Each participating child undergo a joint assessment by a pediatrician, a rehabilitation doctor, a child psychiatrist, a speech therapist, a physical therapist, an occupational therapist, and a social worker. Once the diagnosis of developmental delay is confirmed, the child will be scheduled for prescribed family-based early intervention in the same hospital. Children (between 2 to 4 years old) who attend the program will be enrolled in this study. Informed consent will be obtained from the children and their primary caregivers after they received a complete description of the study. The participants are categorized into three different groups based on their intervention method. The choice of intervention method will be according to the willingness and expedience of the children's caregivers.

Enrollment

45 patients

Sex

All

Ages

2 to 4 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Children with Developmental Delay
  • The caregivers are able to participate in the treatment program

Exclusion criteria

  • Autism
  • Cerebral palsy

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

45 participants in 3 patient groups

Day-Care early intervention program
Experimental group
Description:
The daily treatment session had eight children along with their major caregivers. The treatment was conducted by two experienced occupational therapists (OT), and each session lasted for four hours in the week-day morning with a 10-minute break. The goal of the sessions was to enhance children's development through cognitive training, behavioral modification plan and parenting skill training. Said therapists assisted the caregivers in improving their nurturing and parenting skills with their children, as well as their techniques with regards to influencing them.
Treatment:
Behavioral: Day-Care early intervention program
OPD+SI intervention program
Experimental group
Description:
The treatment program had eight children along with their major caregivers. The treatment was also performed by two experienced OT, and each session lasted for one hours, once a week. The sessions consisted of cognitive training, behavioral modification plan and parenting skill training. Adjunctive SI therapy was also performed by said OT for improving children's sensory motor development in an additional hour.
Treatment:
Behavioral: OPD+SI intervention program
OPD intervention program
Active Comparator group
Description:
The treatment program had eight children along with their major caregivers. The treatment was also performed by two experienced OT, and each session lasted for one hours, once a week. The sessions consisted of cognitive training, behavioral modification plan and parenting skill training.
Treatment:
Behavioral: OPD intervention program

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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