A Controlled Study of Parent Training in the Treatment of ADHD in Young Children
NCT01684644, Not applicable, Completed, University of Aarhus
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | A Controlled Study of Parent Training in the Treatment of ADHD in Young Children | ClinicalTrials.gov |
| NCT number | NCT01684644 | ClinicalTrials.gov |
| Status | Completed | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 164 participants, actual | ClinicalTrials.gov |
| Lead sponsor | University of Aarhus | ClinicalTrials.gov |
| Conditions | Attention Deficit Hyperactivity Disorder | ClinicalTrials.gov |
| Interventions | New Forest Parenting Programme, Treatment as usual | ClinicalTrials.gov |
| First posted | 2012-09-13 | ClinicalTrials.gov |
| Last updated | 2017-07-02 | ClinicalTrials.gov |
Registered outcomes 15
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | ADHD Rating Scale IV-Preschool Version | T1 (at baseline), T2 (twelve weeks from T1), T3 (6 months from T1) | A screening instrument for the symptoms of AD/HD in the preschool population. | ClinicalTrials.gov |
| Secondary | Preschool ADHD-RS (Teacher completed) 18 items | T1 (at baseline), T2 (twelve weeks from T1), T3 (6 months from T1) | screening instrument for the symptoms of AD/HD in the preschool population. | ClinicalTrials.gov |
| Secondary | Strength and Difficulties Questionnaire (parent version) | T1 (at baseline), T2 (twelve weeks from T1), T3 (6 months from T1) | A brief measure of prosocial behaviour and and psychopathology of 3-16 year olds that can be completed by parents | ClinicalTrials.gov |
| Secondary | Strength and Difficulties Questionnaire (teacher completed) | T1 (at baseline), T2 (twelve weeks from T1), T3 (6 months from T1) | A brief measure of prosocial behaviour and and psychopathology of 3-16 year olds that can be completed by teachers | ClinicalTrials.gov |
| Secondary | Child solo play - observation measure - | T1 (at baseline), T2 (twelve weeks from T1), T3 (6 months from T1) | Observation measure: Index of Attention scale assessed from 'time on task'/no. of switches in activity' with high scores representing more attention and less switching | ClinicalTrials.gov |
| Secondary | Child Health Questionnaire (CHQ-28) | T1 (at baseline), T2 (twelve weeks from T1), T3 (6 months from T1) | Quality of life measure | ClinicalTrials.gov |
| Secondary | Family Strain Index 6 items | T1 (at baseline), T2 (twelve weeks from T1), T3 (6 months from T1) | Short screening instrument for the detection of family strain | ClinicalTrials.gov |
| Other | Parental report on somatic complaints in preschool children | T1 (at baseline), T2 (twelve weeks from T1), T3 (6 months from T1) | Parental report on somatic complaints in preschool children (Domenech-Llaberia et al., 2004) | ClinicalTrials.gov |
| Other | 6. The Adult ADHD self-report scale (ASRS-V1.1) 18 items The Adult ADHD self-report scale (ASRS-V1.1) 18 items | T1 (Baseline) | Adult ADHD screening instrument | ClinicalTrials.gov |
| Other | Parent sense of competence scale (PSOC) (17 items) | T1 (at baseline), T2 (twelve weeks from T1), T3 (6 months from T1) | Instrument to assess perceived sense of parenting competence | ClinicalTrials.gov |
| Other | Maternal expressed emotion - 5 min speech sample. | T1 (at baseline), T2 (twelve weeks from T1), T3 (6 months from T1) | A 5-min speech sample obtained from mothers, rated over 6 scales with an overall high score indicating a negative influence on the child. | ClinicalTrials.gov |
| Other | GIPCI (Jigsaw/Tidy up/Freeplay) observation measure | T1 (at baseline), T2 (twelve weeks from T1), T3 (6 months from T1) | GIPCI (Jigsaw/Tidy up/Freeplay) observation measure of parent child interaction with global ratings (0-5) for parent and child behaviours | ClinicalTrials.gov |
| Other | General Health Questionnaire (12 item) | T1 (at baseline), T2 (twelve weeks from T1), T3 (6 months from T1) | Screening instrument to detect psychiatric disorders in adults | ClinicalTrials.gov |
| Other | Neuropsychological test battery | T1 (at baseline), T2 (twelve weeks from T1) | Working memory (verbal and visuospatial) measured by Word span Forward and Backward as well as using Finger Windows Forward and Backward. Inhibition measured using a modified four picture pairs Stroop Task as well as the Head-Toes-Knees-Shoulders task. Flexibility measured using the Switching, Inhibition, and Flexibility Task as well as the Trails-P. Delay-related behavior measured with the Cookie Delay Task and the Teddy Delay Task Simple information processing time measured using the Fish task. In addition, video recordings of the neuropsychological evaluation will be coded and analyzed (private speech and behavior) after the test session | ClinicalTrials.gov |
| Other | Behavior Rating Inventory of Executive Function - Preschool Version [BRIEF-P] | T1 (at baseline), T2 (twelve weeks from T1), T3 (6 months from T1) | ClinicalTrials.gov |
Outcomes 0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as | Source |
|---|
Results by group 0
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units | Source |
|---|
Participant flow 0
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted | Source |
|---|
Adverse events 0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events | Source |
|---|
Adverse event totals 0
The totals the trial posted for each group.
| Total | Group | Affected | At risk | Source |
|---|
Papers 3
The papers the trial lists on ClinicalTrials.gov.
Grants 0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years | Source |
|---|
Trial comparisons 0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|
Tests 2
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|---|---|
| Stroop Color-Word Test | Other outcome | ConductCognition |
| Word Span Task | Other outcome | ConductCognition |
Source 5
| Field | Value | Source |
|---|---|---|
| Release | trials-2026-11-12-0.4.0 | ClinicalTrials.gov |
| Release manifest SHA-256 | 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4 | ClinicalTrials.gov |
| Registry capture | 2026-11-12 | ClinicalTrials.gov |
| Results copy, AACT | 2026-03-23 | ClinicalTrials.gov |
| NIH clinical studies file | 2026-11-13 | ClinicalTrials.gov |
Release trials-2026-11-12-0.4.0
ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)