ClinicalTrials.gg
CompletedNCT01768533TIDEUpdated Jan 15, 2013

Pediatric Behavioral Informatics to Prevent Cancer

An observational study in Obesity, sponsored by University of Massachusetts, Boston. Completed at 1 site in United States. Open to participants aged 21 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2013-01-15.

Sponsored by University of Massachusetts, Boston · Observational

Study type
Observational
Model
Family-based
Time perspective
Cross-sectional
Enrollment
305
Ages
21 Years and older
Sex
All
01

Study summary

The goal of this study is to do formative research which will lead ultimately to the development of a computer-based system called Tailored Information for Diet and Exercise or TIDE for short. TIDE will target energy balance behaviors to prevent the onset of obesity in children. The system will be used by physicians and parents/primary care givers in pediatric primary care practices with the aim of improving parent-pediatrician interactions related to counseling and anticipatory guidance on energy balance behaviors. The aim of this study is to develop a one-two page, paper-pencil proxy questionnaire that is used to query the parent of the child in the waiting room and assesses topic areas related to energy balance behaviors (EBB). The questionnaire will be referred to as the energy balance behaviors questionnaire (EBB-Q). This will require focus groups, cognitive testing of the questionnaire, and survey administration.

02

Conditions studied

  • Obesity

Keywords

  • pediatric
  • obesity
  • prevention
  • health behaviors
  • guidelines
03

In context

Obesity

6,570 studies on the registry are indexed under Obesity; 1,718 are open to participants now.

This study's enrollment of 305 is above the median of 132 across 1,338 observational studies indexed under Obesity.

Browse Obesity studies →

Lead sponsor

University of Massachusetts, Boston is the lead sponsor of 23 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
21 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

General population of parents with children ages 4-10 years who reside in the Greater Boston area. Parents are defined as primary care givers or legal guardians who take primary responsibility for the child's health which includes attending the child's well-care visits.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • primary care givers or legal guardians of children 4-10 years of age who has attended the last two well-child visits with their child

Exclusion criteria

Exclusion Criteria:

  • parent cares for a child who is on a special diet prescribed by pediatrician
05

Study design

Observational model
Family-based
Time perspective
Cross-sectional
Enrollment
305 participants (actual)
Patient registry
No

Groups and cohorts

  • Survey

    A lifestyle survey was administered to primary-care givers or legal guardians who take their children 4-10 y/o to the pediatric well-child visits.

06

What researchers measure

Primary outcomes

  1. sugar-sweetened beverages

    Behavioral outcome measure of the amount of sugar-sweetened beverages consumed.

    Time frame: one time point (baseline only)

Secondary outcomes

  1. BMI

    weight status as defined by body mass index (BMI)

    Time frame: one time point (baseline only)

Other outcomes

  1. Physical activity

    amount of time spent in moderate or greater physical activity

    Time frame: one time point (baseline only)

  2. fruit and vegetables

    amount of fruit servings and vegetable servings consumed per day.

    Time frame: one time point (baseline only)

  3. screen time

    amount of time spent watching television or recreational videos or computers

    Time frame: one time point (baseline only)

07

Study locations

1 site
  • UMass Boston
    Boston, Massachusetts 02155, United States
08

References and documents

Publications

  • Wright JA, Whiteley JA, Watson BL, Sheinfeld Gorin SN, Hayman LL. Tailored communications for obesity prevention in pediatric primary care: a feasibility study. Health Educ Res. 2018 Feb 1;33(1):14-25. doi: 10.1093/her/cyx063. PubMed 29112721 ↗
  • Wright JA, Adams WG, Laforge RG, Berry D, Friedman RH. Assessing parental self-efficacy for obesity prevention related behaviors. Int J Behav Nutr Phys Act. 2014 Apr 22;11:53. doi: 10.1186/1479-5868-11-53. PubMed 24750693 ↗
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 15, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT01768533
Lead sponsor
University of Massachusetts, Boston
Responsible party
Julie Wright (Assistant Professor, University of Massachusetts, Boston) — Principal investigator
First posted
Jan 15, 2013
Start date
Sep 2009
Primary completion
Aug 2011
Completion
Aug 2011
Last update
Jan 15, 2013

Study contacts

Julie A Wright, PhD
principal investigator · UMass Boston

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2013. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion