Skip to content

Can support in time help pre-school children in developing time-processing ability?

Evaluation of a model for early intervention using remediation and time aids for pre-school children with disabilities

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN85136134
Enrollment
151
Registered
2016-01-13
Start date
2016-01-15
Completion date
Unknown
Last updated
2023-01-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Childhood disability and developmental delay Mental and Behavioural Disorders Childhood disability and developmental delay

Interventions

Each school is initially assigned as being in the control group or intervention group. After baseline assessments have been made (first two weeks of study), the children in the intervention group unde

Sponsors

Centre for Clinical Research Dalarna
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Current participant inclusion criteria as of 25/05/2020: 1. Either 1.1. Children with disabilities like CP, MMC, AST, ADHD, ID and developmental delays, or 1.2. Typically Developing children (included as of 02/09/2019) 2. Aged 5 or 6 years during the year of the intervention Previous participant inclusion criteria: 1. Children with disabilities like CP, MMC, AST, ADHD, ID and developmental delays 2. Aged 5 or 6 years during the year of the intervention

Exclusion criteria

Exclusion criteria: 1. Multiple disabilities 2. Severe communication problems

Design outcomes

Primary

MeasureTime frame
Time-processing ability (TPA) is measured using the Kit for Assessment of Time-processing ability (KaTid) at baseline, after the 8 week intervention period and then a third data collection for the control group after their completion of the 8 week intervention.

Secondary

MeasureTime frame
Everyday functioning is measured using the Time-Parent scale, Autonomy scale and ABAS-II questionnaires at baseline, after the 8 week intervention period and then a third data collection for the control group after their completion of the 8 week intervention.

Countries

Sweden

Contacts

Public ContactSara Wallin Ahlström
sara.wallin@regiondalarna.se+46 73 3643235

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 5, 2026