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Efficacy of Omega-3/Omega-6 Fatty Acids in Pre-school Children at Risk for ADHD

Primary Purpose

Children With ADHD Symptoms >90th Percentile (FBB-ADHS-V); no Beginning or Completion of Psychotherapeutically or Psychopharmalogical Treatment During the Study

Status
Unknown status
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
omega-3/omega-6 fatty acids (PUFAs)
Sponsored by
University of Cologne
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Children With ADHD Symptoms >90th Percentile (FBB-ADHS-V); no Beginning or Completion of Psychotherapeutically or Psychopharmalogical Treatment During the Study focused on measuring omega-3/omega-6 fatty acids, Pre-school children with ADHD symptoms, randomized controlled trial

Eligibility Criteria

3 Years - 6 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age: 3 - 6 years
  • Visit of a preschool (Kindergarten)
  • Parents have a command of the German language
  • Screening score >90th percentile in a combined parent and teacher screening questionnaire

Exclusion Criteria:

  • Hypersensitivity or inability to components of the study product (fish oil, primrose oil, natural strawberry flavouring, bovine gelatine)
  • Consumption of omega fatty acids preparation
  • Consumption of fish oil-capsules

Sites / Locations

  • Department of Child and Adolescent Psychiatry at the University CologneRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

omega-3/omega-6 fatty acids (PUFAs)

placebo without PUFAs

Arm Description

Equazen 500mg/day= 116 mg docosahexaenoic acid, 372 mg Eicosapentaenoic acid, 40 mg gamma-Linolenic acid

Placebo without PUFAs

Outcomes

Primary Outcome Measures

Change in Symptom Checklist for pre-school children with ADHD symptoms (FBB-ADHS-V) total score rated by parents and teachers
The FBB-ADHS-V Questionnaire is a developed parent and teacher rating scale which assesses several factors of hyperactivity, impulsivity and inattention problems in pre-school or at home.

Secondary Outcome Measures

Change in ODD symptoms -parent/ teacher rated (FBB-ADHD-V)
Change in Child Behavior Checklist (CBCL) and Teacher Report Form (TRF)
The CBCL and the TRF are well evaluated rating scales for the assessement of a broad spectrum of child behavioral and emotional problems as perceived by parents and teachers respectively
Diagnostic checklist for ADHD (DCL-ADHS) and diagnostic checklist for odd (DCL-SSV)
The DCL-ADHD and the DCL-ODD are external assessment questionnaires. Parents were asked 18 questions to hyperactivity, impulsivity and inattention by the rater or to symptom criteria for ODD.
Change in intelligence: Sequential & Simultaneous Processing, Achievement (K-ABC)
The Kaufman Assessment Battery for Children (K-ABC) is a standardized test that assesses intelligence and achievement in children aged 2;6 to 12;6 years. It is comprised of four global test scores that include: sequential processing scales, simultaneous processing scales, achievement scales and mental processing composite. There is an additional nonverbal scale.

Full Information

First Posted
February 16, 2013
Last Updated
March 14, 2017
Sponsor
University of Cologne
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1. Study Identification

Unique Protocol Identification Number
NCT01795040
Brief Title
Efficacy of Omega-3/Omega-6 Fatty Acids in Pre-school Children at Risk for ADHD
Official Title
Efficacy of a Supplementary Balanced Diet With Omega-3/ Omega-6 Fatty Acids Among 3-6 Year Olds With Symptoms of ADHD
Study Type
Interventional

2. Study Status

Record Verification Date
March 2017
Overall Recruitment Status
Unknown status
Study Start Date
September 2010 (undefined)
Primary Completion Date
April 2017 (Anticipated)
Study Completion Date
May 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Cologne

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The efficacy of PUFAs (as nutritional supplement) in/for pre-school children with ADHS symptoms will be evaluated in a randomised controlled doubleblind trail with children aged 3-6 years.
Detailed Description
The study aims at the reduction of hyperactivity, inattention and impulsivity in pre-school children aged 3-6 years, visiting a preschool, and the prevention of clinical ADHD symptoms. The 3-6 years old children will be identified by a combined parent and teacher rating ADHD-symptoms questionnaire (FBB-ADHS-V). Children with ADHD symptoms >90th percentile will participate in a following diagnostic process. The children (n = 150) will be randomised doubleblind to a control group (taking every day four capsules Equazen eye q, containing 400 mg fish oil and 100mg evening primrose oil - EPA (372mg), DHA (116mg), GLA (40mg) and vitamin E (7.2 mg) ) or placebo group. The study is divided into two phases with four months each. After unblinding after the first phase pre-school children taking placebo receive Omega-3/Omega-6 Fatty Acids. Children (n = 75) taking verum during first four months will be randomised doubleblind to verum or placebo. In this way the progress of the behaviour symptoms will be evaluated after a significant period of time (eigth months). Clinical examination (questionnaires, intelligence test, medical examination) and evaluation of ADHD symptoms through parents and teachers with several questionnaires will be used before beginning, after four months and after eight months. In addition the pre-school children will be taken a blood sample (finger prick test) to measure the omega-3/omega-6 fatty acids levels. Additionally regular phone calls will be implemented. Medical examinations and meetings will taken place if required. If symptoms increase, children will be treated medical and/ or psychotherapeutically.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Children With ADHD Symptoms >90th Percentile (FBB-ADHS-V); no Beginning or Completion of Psychotherapeutically or Psychopharmalogical Treatment During the Study
Keywords
omega-3/omega-6 fatty acids, Pre-school children with ADHD symptoms, randomized controlled trial

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
omega-3/omega-6 fatty acids (PUFAs)
Arm Type
Experimental
Arm Description
Equazen 500mg/day= 116 mg docosahexaenoic acid, 372 mg Eicosapentaenoic acid, 40 mg gamma-Linolenic acid
Arm Title
placebo without PUFAs
Arm Type
Placebo Comparator
Arm Description
Placebo without PUFAs
Intervention Type
Dietary Supplement
Intervention Name(s)
omega-3/omega-6 fatty acids (PUFAs)
Other Intervention Name(s)
Equazen Eye Q
Intervention Description
Equazen 500mg/day= 116 mg docosahexaenoic acid, 372 mg Eicosapentaenoic acid, 40 mg gamma-Linolenic acid
Primary Outcome Measure Information:
Title
Change in Symptom Checklist for pre-school children with ADHD symptoms (FBB-ADHS-V) total score rated by parents and teachers
Description
The FBB-ADHS-V Questionnaire is a developed parent and teacher rating scale which assesses several factors of hyperactivity, impulsivity and inattention problems in pre-school or at home.
Time Frame
Change from pre- assessment to post assessment four months after treatment begin and to post assessment eight months after treatment begin
Secondary Outcome Measure Information:
Title
Change in ODD symptoms -parent/ teacher rated (FBB-ADHD-V)
Time Frame
Change from pre- assessment to post assessment four months after treatment begin and to post assessment eight months after treatment begin
Title
Change in Child Behavior Checklist (CBCL) and Teacher Report Form (TRF)
Description
The CBCL and the TRF are well evaluated rating scales for the assessement of a broad spectrum of child behavioral and emotional problems as perceived by parents and teachers respectively
Time Frame
Change from pre- assessment to post assessment four months after treatment begin.
Title
Diagnostic checklist for ADHD (DCL-ADHS) and diagnostic checklist for odd (DCL-SSV)
Description
The DCL-ADHD and the DCL-ODD are external assessment questionnaires. Parents were asked 18 questions to hyperactivity, impulsivity and inattention by the rater or to symptom criteria for ODD.
Time Frame
Change from pre- assessment to post assessment four months after treatment begin and to post assessment eight months after treatment begin
Title
Change in intelligence: Sequential & Simultaneous Processing, Achievement (K-ABC)
Description
The Kaufman Assessment Battery for Children (K-ABC) is a standardized test that assesses intelligence and achievement in children aged 2;6 to 12;6 years. It is comprised of four global test scores that include: sequential processing scales, simultaneous processing scales, achievement scales and mental processing composite. There is an additional nonverbal scale.
Time Frame
Change from pre- assessment to post assessment four months after treatment begin.
Other Pre-specified Outcome Measures:
Title
finger prick test to measure the PUFA blood concentration
Description
It will taken a blood sample (finger prick test) to measure the omega-3/omega-6 fatty acids levels.
Time Frame
Change from pre- assessment to post assessment four months after treatment begin

10. Eligibility

Sex
All
Minimum Age & Unit of Time
3 Years
Maximum Age & Unit of Time
6 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age: 3 - 6 years Visit of a preschool (Kindergarten) Parents have a command of the German language Screening score >90th percentile in a combined parent and teacher screening questionnaire Exclusion Criteria: Hypersensitivity or inability to components of the study product (fish oil, primrose oil, natural strawberry flavouring, bovine gelatine) Consumption of omega fatty acids preparation Consumption of fish oil-capsules
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Manfred Doepfner, Prof. Dr.
Email
Manfred.doepfner@uk-koeln.de
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Manfred Doepfner, Prof. Dr.
Organizational Affiliation
Department of Child and Adolescent Psychiatry Univ. Cologne
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Child and Adolescent Psychiatry at the University Cologne
City
Cologne
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Manfred Doepfner, Prof. Dr.
Email
Manfred.doepfner@uk-koeln.de

12. IPD Sharing Statement

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Efficacy of Omega-3/Omega-6 Fatty Acids in Pre-school Children at Risk for ADHD

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