The PAC Study: Parents as Agents of Change in Pediatric Weight Management (PAC)

February 19, 2014 updated by: Geoff Ball, University of Alberta

The Canadian pediatric obesity epidemic has led to great interest in evaluating weight management care for obese children and families. Investigation is warranted since obesity is linked to risk factors for chronic diseases including type 2 diabetes mellitus (T2DM) and cardiovascular disease (CVD). Over the past 25 years, many interventions have studied the role of healthy lifestyle behaviours to help obese children achieve and maintain a healthy weight. A contemporary view of pediatric weight management interventions includes parents as a fundamental recipient of treatment. These interventions recognize the influence parents have on the lifestyle behaviours of their children. While such parent-based interventions have helped establish the role of education and behavioural theory in facilitating lifestyle changes, we believe an equally important intervention element is a focus on the role of cognitions in helping to interpret behaviour change and change maintenance. Our study incorporates cognitive behaviour theory (CBT) into an intervention for parents of obese children and compares it to a more traditional modality based on psycho-education (PEP).

Hypothesis: Obese 8 - 12 year old children (n=45) whose parents complete a 16-session, group-based, CBT intervention will achieve greater reductions in adiposity as well as improvements in physiological risk factors for T2D, lifestyle behaviours, and psychosocial outcomes at post-intervention as well as 6- and 12-months follow-up versus children (n=45) whose parents complete a 16-session, group-based, psycho-education intervention .

Primary Objective: To compare the impact of two weight management interventions (CBT versus PEP) for parents of obese children on child BMI z-score.

Secondary Objective: To measure a comprehensive set of physiological, behavioural and psychosocial outcomes in obese children and parents pre- and post-intervention.

We expect obese children whose parents complete the CBT intervention will experience greater reductions in BMI z-score vs. children whose parents complete the PEP intervention. We anticipate that improvements in parenting style, family stress, and lifestyle behaviours will be important to improve adiposity, lifestyle behaviours, and risk factors for T2DM and CVD in obese children.

Study Overview

Study Type

Interventional

Enrollment (Actual)

63

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Alberta
      • Edmonton, Alberta, Canada, T5K 0L4
        • Pediatric Centre for Weight and Health

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

8 years to 12 years (Child)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria: Boys and girls (n = 90) between 8 - 12 years of age with a sex- and age-specific BMI ≥95th percentile are eligible for this study. Children are referred to the Pediatric Centre for Weight and Health (PCWH) at the Stollery Children's Hospital (SCH) (Edmonton, AB, Canada) only if their BMI percentile meets or exceeds this threshold. At least one parent/guardian per family is required to participate in one of the two group-based interventions as agents of change for their family.

Exclusion Criteria: Obese children referred to the PCWH <8 years old will be referred to an outpatient dietitian for nutrition counselling; obese boys and girls >12 years old will be eligible for other weight management interventions at the PCWH. Children who do not have a parent/guardian interested in participating or possess an age- and sex-specific BMI <95th percentile will be ineligible. Children diagnosed with an endocrine disorder (i.e., Polycystic Ovarian Syndrome, Prader-Willi Syndrome, hypothyroidism) will be referred to the Endocrine Clinic at the SCH. Parents or children who are identified at screening as having severe mental health conditions or psychosocial circumstances that could limit their ability to participate in the interventions will be referred to appropriate agencies and services. Impaired ability to participate in either intervention may include substantial difficulties in attendance or implementing changes at home. Referral services may include psychological/psychiatric services, welfare services, and private nutrition or exercise counselling. Dr. Rachel Keaschuk (PCWH Psychologist and Co-I) will perform psychological interviews (75 - 90 minutes) with all families to determine family appropriateness and will lead family discussions regarding referral services (if indicated).

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Cognitive Behavioural Therapy (CBT)
Group-based lifestyle counseling for parents
Clinical research supports the use of CBT-based interventions in weight management for adults and children. However, the current study will advance the existing knowledge-base by combining CBT with the parents as agents of change approach for pediatric weight management. CBT is a theoretically-based therapy that focuses on the role that cognitive processes play in the maintenance of problem behaviours, mood states, and habits. CBT highlights the relationship between thoughts, feelings and actions, and utilizes techniques involving motivation, goal-setting, problem-solving, and knowledge/skill acquisition that can facilitate sustainable behaviour changes.
Other Names:
  • CBT
PEP is a knowledge-based intervention that is modelled after traditional nutrition and health education programs. Research has demonstrated that knowledge based programs can improve health behaviours and outcomes in overweight and obese populations. In relation to CBT, PEP is a more passive intervention and there is limited focus on active skill building. While PEP does not represent a true control group, its content and delivery are consistent with what many clinicians provide for weight management.
Other Names:
  • PEP
Experimental: Psycho-Education Program (PEP)
Group-based lifestyle counseling for parents
Clinical research supports the use of CBT-based interventions in weight management for adults and children. However, the current study will advance the existing knowledge-base by combining CBT with the parents as agents of change approach for pediatric weight management. CBT is a theoretically-based therapy that focuses on the role that cognitive processes play in the maintenance of problem behaviours, mood states, and habits. CBT highlights the relationship between thoughts, feelings and actions, and utilizes techniques involving motivation, goal-setting, problem-solving, and knowledge/skill acquisition that can facilitate sustainable behaviour changes.
Other Names:
  • CBT
PEP is a knowledge-based intervention that is modelled after traditional nutrition and health education programs. Research has demonstrated that knowledge based programs can improve health behaviours and outcomes in overweight and obese populations. In relation to CBT, PEP is a more passive intervention and there is limited focus on active skill building. While PEP does not represent a true control group, its content and delivery are consistent with what many clinicians provide for weight management.
Other Names:
  • PEP

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Child BMI Z-score
Time Frame: Pre-intervention
Pre-intervention
Child BMI Z-score
Time Frame: post-intervention
post-intervention
Child BMI Z-score
Time Frame: 6-months post-intervention
6-months post-intervention
Child BMI Z-score
Time Frame: 12-months post-intervention
12-months post-intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Lifestyle behaviours
Time Frame: Pre-intervention
Nutrition (4-day food records; child and parent) and physical activity (7-day pedometer logs; child and parent) behaviours
Pre-intervention
Parental stress
Time Frame: Pre-intervention
Parental stress index (PSI)
Pre-intervention
Cardiometabolic risk factors
Time Frame: Pre-intervention
Blood pressure, fasting glucose, fasting insulin, HDL-C, LDL-C, total cholesterol, triglycerides (child only)
Pre-intervention
Family functioning
Time Frame: Pre-intervention
Family Adaptability and Cohesion Scale-IV (FACES-IV); completed by parents
Pre-intervention
Lifestyle behaviours
Time Frame: post-intervention
Nutrition (4-day food records; child and parent) and physical activity (7-day pedometer logs; child and parent) behaviours
post-intervention
Lifestyle behaviours
Time Frame: 6-months post-intervention
Nutrition (4-day food records; child and parent) and physical activity (7-day pedometer logs; child and parent) behaviours
6-months post-intervention
Lifestyle behaviours
Time Frame: 12-months post-intervention
Nutrition (4-day food records; child and parent) and physical activity (7-day pedometer logs; child and parent) behaviours
12-months post-intervention
Parental stress
Time Frame: post-intervention
Parental stress index (PSI)
post-intervention
Parental stress
Time Frame: 6-months post-intervention
Parental stress index (PSI)
6-months post-intervention
Parental stress
Time Frame: 12-months post-intervention
Parental stress index (PSI)
12-months post-intervention
Cardiometabolic risk factors
Time Frame: post-intervention
Blood pressure, fasting glucose, fasting insulin, HDL-C, LDL-C, total cholesterol, triglycerides (child only)
post-intervention
Cardiometabolic risk factors
Time Frame: 6-months post-intervention
Blood pressure, fasting glucose, fasting insulin, HDL-C, LDL-C, total cholesterol, triglycerides (child only)
6-months post-intervention
Cardiometabolic risk factors
Time Frame: 12-months post-intervention
Blood pressure, fasting glucose, fasting insulin, HDL-C, LDL-C, total cholesterol, triglycerides (child only)
12-months post-intervention
Family functioning
Time Frame: post-intervention
Family Adaptability and Cohesion Scale-IV (FACES-IV); completed by parents
post-intervention
Family functioning
Time Frame: 6-months post-intervention
Family Adaptability and Cohesion Scale-IV (FACES-IV); completed by parents
6-months post-intervention
Family functioning
Time Frame: 12-months post-intervention
Family Adaptability and Cohesion Scale-IV (FACES-IV); completed by parents
12-months post-intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Geoff Ball, PhD, RD, University of Alberta
  • Principal Investigator: Amanda Newton, PhD, RN, University of Alberta

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

September 1, 2010

Primary Completion (Actual)

September 1, 2013

Study Completion (Actual)

January 1, 2014

Study Registration Dates

First Submitted

December 16, 2010

First Submitted That Met QC Criteria

December 23, 2010

First Posted (Estimate)

December 24, 2010

Study Record Updates

Last Update Posted (Estimate)

February 20, 2014

Last Update Submitted That Met QC Criteria

February 19, 2014

Last Verified

February 1, 2014

More Information

Terms related to this study

Other Study ID Numbers

  • PCWH01-2009
  • CIHR-MSH83715 (Other Grant/Funding Number: Funded by the Canadian Institutes of Health Research (CIHR))

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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