NCT00862147

Brief Summary

The objective of this study is to evaluate the effect of the International Child Development Program (ICDP). Research questions to be answered:

  1. 1.Does the ICDP affect children's psychosocial functioning compared to treatment as usual?
  2. 2.Does the ICDP change parent-child interaction?

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
35

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jan 2007

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
terminated

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2007

Completed
2.2 years until next milestone

First Submitted

Initial submission to the registry

March 13, 2009

Completed
3 days until next milestone

First Posted

Study publicly available on registry

March 16, 2009

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2009

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2009

Completed
Last Updated

February 14, 2017

Status Verified

February 1, 2017

Enrollment Period

2.7 years

First QC Date

March 13, 2009

Last Update Submit

February 13, 2017

Conditions

Keywords

Child psychosocial Functioning

Outcome Measures

Primary Outcomes (1)

  • psychosocial functioning

    study terminated

Study Arms (2)

ICDP

EXPERIMENTAL

International Child Development Program

Behavioral: ICDP

Treatment as usual

ACTIVE COMPARATOR

Treatment as usual

Behavioral: Treatment as usual

Interventions

ICDPBEHAVIORAL

Parent training group

Also known as: International Child Development Program
ICDP

Parent and/or child focused interventions

Treatment as usual

Eligibility Criteria

Age4 Years - 4 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17)

You may qualify if:

  • SDQ \>/= 9, subjective treatment need

You may not qualify if:

  • Already in treatment

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Norwegian University of Science and Technology

Trondheim, Norway

Location

MeSH Terms

Interventions

Therapeutics

Study Officials

  • Lars Wichstrom

    Norwegian University of Science and Technology

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

March 13, 2009

First Posted

March 16, 2009

Study Start

January 1, 2007

Primary Completion

September 1, 2009

Study Completion

September 1, 2009

Last Updated

February 14, 2017

Record last verified: 2017-02

Locations