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"Mandometer®" Study for Managing Childhood Obesity

Primary Purpose

Childhood Obesity

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Mandometer
Lifestyle
Sponsored by
University of Bristol
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Childhood Obesity focused on measuring Childhood, Obesity, Behavior modification, Insulin resistance

Eligibility Criteria

10 Years - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Obese children and adolescents aged 10-18

Exclusion Criteria:

Children:

  • Having associated learning difficulties
  • Who have received medication for associated insulin resistance
  • Refusal of parent/legal guardian to give informed consent.

Sites / Locations

  • Bristol Royal Hospital for Children

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Mandometer

Control

Arm Description

Active intervention - one meal eaten per day off Mandometer

Nutritional and activity advice alone

Outcomes

Primary Outcome Measures

BMI SDS or Z-score
Body Mass Index standard deviation (s.d.) scores also called Z-scores, are measures of relative weight adjusted for a child's age and sex. In terms of this score for weight management, a lower score would be viewed a beneficial outcome at the end of the intervention. The change in BMI SDS was calculated as the value at 12 months minus value at baseline ( a negative score being beneficial).

Secondary Outcome Measures

Insulin Sensitivity
Insulin sensitivity was measured by the homeostasis model assessment (HOMA-R) equation: HOMA-R = fasting glucose (mmol/l) × fasting insulin (mIU/l)/22.5. The lower the HOMA-R, the more insulin sensitive the participant is which is considered beneficial to metabolic health.
Speed Food Consumed
Grams of food eaten per minute in Mandometer® arm compared to standard arm at baseline and 12 months. Reducing speed of eating improves satiety and reduces total food consumed at meals in our overall hypothesis.
Percentage Body Fat (Measured Using a Tanita Bio-impedance Monitor Model BC-418MA)
Change in % body fat. Calculated as %body fat at end of intervention minus baseline. A negative value being viewed as beneficial outcome.

Full Information

First Posted
December 1, 2006
Last Updated
September 27, 2019
Sponsor
University of Bristol
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1. Study Identification

Unique Protocol Identification Number
NCT00407420
Brief Title
"Mandometer®" Study for Managing Childhood Obesity
Official Title
Can a Novel Treatment Using "Mandometer®" Technology Improve Weight Loss in a Childhood Obesity Clinic?
Study Type
Interventional

2. Study Status

Record Verification Date
September 2019
Overall Recruitment Status
Completed
Study Start Date
September 2004 (undefined)
Primary Completion Date
October 2009 (Actual)
Study Completion Date
January 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Bristol

4. Oversight

5. Study Description

Brief Summary
We run a successful clinic in Bristol for children with severe obesity who already demonstrate many features to suggest they are at increased risk of early diabetes and heart disease. However, we have found that young children respond better to simple interventions than do adolescents. We have used a new treatment regimen "Mandometer®" to help our most difficult adolescent cases lose weight. We would like to do a study to see if all adolescents might improve weight loss using this technology compared to what we routinely offer
Detailed Description
Childhood obesity is rapidly reaching epidemic proportions in the United Kingdom. Recent studies have indicated a prevalence level for obesity of 15% at 15 years of age. The implications for metabolic, cardiovascular and cancer risk in later life are enormous. The International Obesity Task Force (IOTF) and the European Association for the Study of Obesity (EASO) have identified childhood obesity as a matter for urgent attention. However, there are very few obesity clinics for children in the UK and effective treatment regimens are simply not available. We have developed an obesity clinic at the Royal Hospital for Children in Bristol and observed effective weight reduction in pre-pubertal children. Our simple treatment framework has proved far less effective in adolescence. We have therefore collaborated with an eating disorder clinic from the Karolinska Institute in Sweden to develop a novel therapy to treat obesity using modified equipment originally designed to treat adolescents with DSM-IV eating disorders. Pilot data indicate that adolescents are better able to address the issue of weight reduction within this treatment modality. Having established the software and treatment process we now wish to perform a randomised, control trial to test the efficacy of this new treatment against that currently provided.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Childhood Obesity
Keywords
Childhood, Obesity, Behavior modification, Insulin resistance

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Mandometer
Arm Type
Experimental
Arm Description
Active intervention - one meal eaten per day off Mandometer
Arm Title
Control
Arm Type
Active Comparator
Arm Description
Nutritional and activity advice alone
Intervention Type
Device
Intervention Name(s)
Mandometer
Intervention Description
A computerised device, Mandometer, providing real time feedback to participants during meals to slow down speed of eating and reduce total intake; standard lifestyle modification therapy.
Intervention Type
Behavioral
Intervention Name(s)
Lifestyle
Intervention Description
Typical dietary and activity advice as normally provided in clinic (control).
Primary Outcome Measure Information:
Title
BMI SDS or Z-score
Description
Body Mass Index standard deviation (s.d.) scores also called Z-scores, are measures of relative weight adjusted for a child's age and sex. In terms of this score for weight management, a lower score would be viewed a beneficial outcome at the end of the intervention. The change in BMI SDS was calculated as the value at 12 months minus value at baseline ( a negative score being beneficial).
Time Frame
12 months primary/ 18 months secondary outcome
Secondary Outcome Measure Information:
Title
Insulin Sensitivity
Description
Insulin sensitivity was measured by the homeostasis model assessment (HOMA-R) equation: HOMA-R = fasting glucose (mmol/l) × fasting insulin (mIU/l)/22.5. The lower the HOMA-R, the more insulin sensitive the participant is which is considered beneficial to metabolic health.
Time Frame
12 months
Title
Speed Food Consumed
Description
Grams of food eaten per minute in Mandometer® arm compared to standard arm at baseline and 12 months. Reducing speed of eating improves satiety and reduces total food consumed at meals in our overall hypothesis.
Time Frame
12 months
Title
Percentage Body Fat (Measured Using a Tanita Bio-impedance Monitor Model BC-418MA)
Description
Change in % body fat. Calculated as %body fat at end of intervention minus baseline. A negative value being viewed as beneficial outcome.
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Obese children and adolescents aged 10-18 Exclusion Criteria: Children: Having associated learning difficulties Who have received medication for associated insulin resistance Refusal of parent/legal guardian to give informed consent.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Julian P Hamilton-Shield, MD
Organizational Affiliation
University of Bristol and Bristol Royal Hospital for Children
Official's Role
Principal Investigator
Facility Information:
Facility Name
Bristol Royal Hospital for Children
City
Bristol
ZIP/Postal Code
BS2 8AE
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
20051465
Citation
Ford AL, Bergh C, Sodersten P, Sabin MA, Hollinghurst S, Hunt LP, Shield JP. Treatment of childhood obesity by retraining eating behaviour: randomised controlled trial. BMJ. 2009 Jan 5;340:b5388. doi: 10.1136/bmj.b5388.
Results Reference
result

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"Mandometer®" Study for Managing Childhood Obesity

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