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Motivational Interviewing With Dyslipidemic Adolescents Together With a Parent Versus With Adolescents Alone: A Mixed Methods Clinical Trial

Primary Purpose

Dyslipidemias

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Motivational Interviewing/Counselling
Sponsored by
The Hospital for Sick Children
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Dyslipidemias focused on measuring Motivational Interviewing

Eligibility Criteria

10 Years - 17 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age at randomization: 10-17 years old
  • 12 hour fasting lipid profile with triglycerides ≥39 mg/dL (1.0 mmol/L) or HDL-C ≤46 mg/dL (1.2 mmol/L), and with non-HDL-C ≥123 mg/dL (3.2 mmol/L)
  • Waist to height ratio ≥0.5.

Exclusion Criteria:

  • On lipid lowering medication
  • non-English speaking
  • Developmentally delayed

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    Intervention Group

    Control Group - Active Comparator

    Arm Description

    Group A (Parent-adolescent dyads)

    Group B (Adolescents only)

    Outcomes

    Primary Outcome Measures

    Changes in total cholesterol to HDL-C ratio

    Secondary Outcome Measures

    Full Information

    First Posted
    March 31, 2016
    Last Updated
    April 5, 2016
    Sponsor
    The Hospital for Sick Children
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02730559
    Brief Title
    Motivational Interviewing With Dyslipidemic Adolescents Together With a Parent Versus With Adolescents Alone: A Mixed Methods Clinical Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    April 2016
    Overall Recruitment Status
    Completed
    Study Start Date
    November 2012 (undefined)
    Primary Completion Date
    June 2014 (Actual)
    Study Completion Date
    undefined (undefined)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    The Hospital for Sick Children

    4. Oversight

    5. Study Description

    Brief Summary
    The primary focus of this proposal is to address growing concern of overweight/ obese adolescents with hyperlipidemia. The proposed study is a 2-arm randomized controlled clinical trial to compare the effectiveness of Motivational interviewing (MI) interventions with the parent and adolescent dyad versus adolescent (10-17yr) alone. The patients will be recruited from the Lipid clinic at Sick Kids. The study hypothesis is that parent child dyad will have more success due to the possible synergetic effect compared to adolescents alone. The study's primary outcome is cholesterol levels (Triglycerides/HDL ratio) and secondary outcomes include overall improvement in their lifestyle and their responses to the MI intervention.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Dyslipidemias
    Keywords
    Motivational Interviewing

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    32 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Intervention Group
    Arm Type
    Experimental
    Arm Description
    Group A (Parent-adolescent dyads)
    Arm Title
    Control Group - Active Comparator
    Arm Type
    Active Comparator
    Arm Description
    Group B (Adolescents only)
    Intervention Type
    Other
    Intervention Name(s)
    Motivational Interviewing/Counselling
    Intervention Description
    Motivational Interviewing/Counselling
    Primary Outcome Measure Information:
    Title
    Changes in total cholesterol to HDL-C ratio
    Time Frame
    Initial clinic visit (baseline); Repeated 6 months after baseline;

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    10 Years
    Maximum Age & Unit of Time
    17 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Age at randomization: 10-17 years old 12 hour fasting lipid profile with triglycerides ≥39 mg/dL (1.0 mmol/L) or HDL-C ≤46 mg/dL (1.2 mmol/L), and with non-HDL-C ≥123 mg/dL (3.2 mmol/L) Waist to height ratio ≥0.5. Exclusion Criteria: On lipid lowering medication non-English speaking Developmentally delayed

    12. IPD Sharing Statement

    Learn more about this trial

    Motivational Interviewing With Dyslipidemic Adolescents Together With a Parent Versus With Adolescents Alone: A Mixed Methods Clinical Trial

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