ClinicalTrials.gg
Not yet recruitingNCT07937033BRIDGEUpdated Nov 13, 2026

Bridging Rural Inclusion for Dietary Guidance and Education (BRIDGE) Study

An observational study in Eating Behaviors, sponsored by Penn State University. Not yet recruiting at 1 site in United States. Open to participants aged 6 Years to 10 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-11-13.

Sponsored by Penn State University · Observational

Updated Nov 13, 2026Newly registeredGo to Updates ↓

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Study type
Observational
Model
Ecologic or community
Time perspective
Prospective
Enrollment
100
Ages
6 Years to 10 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-14

Among 37 studies in Feeding Behavior by Penn State University — 3 open to participants now, 3 under way, none of them phase 3. Feeding Behavior · Penn State University.

Started
2026
with 1 other
Observational
6 of 37
1 open now
Registered
37th of 37
by date

Among the 37 studies in Feeding Behavior by Penn State University, this one is one of 2 that started in 2026, is one of 6 observational ones, and was the 37th registered.

Feeding Behavior

987 studies on the registry are indexed under Feeding Behavior; 179 are open to participants now.

Browse Feeding Behavior studies →

Open to participants now

3 of the 37 studies in Feeding Behavior by Penn State University are open now, in 1 country. Recruiting first, the newest first:

By country, each count listing its studies:

All 3 open studies →

Where they have run

Who these studies take

Of the 114 Feeding Behavior studies recruiting now, 36 (32%) set no upper age limit and 72 (63%) stop at 75 or younger; 42 take children under 18; 72 take healthy volunteers.

This study: 6 Years to 10 Years · all sexes · healthy volunteers too.

The full table on the hub →

This tab as a report to print or save as PDF → With an account.

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Watch this landscapeDownload CSVNarrow it in search →With an account: a weekly mail of what changed among 37 studies in Feeding Behavior by Penn State University, or all of them as a file.
02

Study summary

This study will test the acceptability and feasibility of the Wear-IT app for sending healthy eating messages and collecting questionnaires, photos, and videos via smart phone.

Read the detailed description

This study will be observational. Recruitment of 100, 6-10-year-old child-parent dyads from rural Appalachia will use approved advertisements on popular internet sites, mom's groups, Facebook, family-oriented periodicals, online recruiting databases (e.g., Research Match) and paid recruitment (Build Clinical, Meta). Interested parents will complete an initial screening via REDCap to determine if families fit the inclusion and exclusion criteria. Prior to answering screening questions, the parents will be provided with a brief study description. Once parents complete the screening questions, they will be scheduled for an Onboarding videoconference call (e.g., Zoom). At the Onboarding session, a parent will sign a full study Consent form and children will provide written Assent. Parents will then select locations on a map to mark their home address and any locations they commonly shop for foods. Researchers will also help parents install the Wear-IT app on their own smartphone devices and complete a training protocol. After the Onboarding session, parents will complete an online survey on demographic information, parental feeding practices via the Child Feeding Questionnaire and the Family Food Behavior Survey, both of which have been validated. Neighborhood Impact on Kids Study questionnaire will be used to assess family food rules and parents' perception of the neighborhood food environment. Child appetitive traits will be assessed using the Children's Eating Behavior Questionnaire, which has been validated against laboratory food intake. Lastly, parent eating behavior will be assessed using the validated Three Factor Eating Questionnaire. Parents will use the Wear-IT app for three weeks. During the 3-week period, parents will receive ecological momentary assessment (EMA) prompts and just-in-time adaptive intervention messages related to the three primary diet-related health behavior categories: 1) home food environment; 2) home meals; and 3) food shopping. Specifically, participants will complete weekly home food inventories and meal videos, at-home meal surveys 3 times a week, and daily end-of-day check-in surveys. They will also be prompted to take a picture of their receipt whenever they go to an identified food shopping location. Parents will rate the acceptability of each of the messages sent via Wear-IT using the Intervention Appropriateness Measure. Upon completion of the 3-week Wear-IT period, parents will repeat the online questionnaire they completed after on-boarding. They will also rate the acceptability and validity of Wear-IT's EMA using the Acceptability of Intervention Measure and the Feasibility of Intervention Measure, respectively.

03

Conditions studied

  • Eating Behaviors

Browse trials for

Keywords

  • Acceptibilty
  • Feasability
  • Appropriateness
04

Who can participate

Ages eligible
6 Years to 10 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Participants will include children and their parents who live in Appalachia.

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

In order to be enrolled, children must:

  • Speak fluent English
  • Be of good health based on parental self-report
  • have no learning (e.g., dyslexia) or neurodevelopmental disabilities (e.g., ADHD)
  • between the ages of 6-10 years-old at enrollment.
  • Live in the Appalachian region of the United States.

Parents will be included if:

  • Speak fluent English
  • They report being the primary parent responsible for feeding decisions
  • Have a smart-phone device that has an active phone service plan
  • Live in the Appalachian region of the United States.

Exclusion criteria

Exclusion criteria:

Children would be excluded if they:

  • Do not speak fluent English
  • are \<6 years old or > 10 years-old at baseline
  • have any of the following: a learning disability, ADD/ADHD, language delays, autism or other neurological or psychological conditions
  • have a pre-existing medical condition such as type I or type II diabetes, rheumatoid arthritis, Cushing's syndrome, Down's syndrome, food allergies, severe lactose intolerance, Prader-Willi syndrome, , cancer, renal failure, or cerebral palsy.
  • Do not live in the Appalachian region of the United States.

Parents will be excluded if:

  • Do not speak fluent English
  • They report not being the primary parent responsible for feeding decisions
  • Does not have a smart-phone device with an active phone service plan
  • Do not live in the Appalachian region of the United States.

Secondary research subjects (other family members who may appear in video and consent to incidental recording): will be excluded if:

  • They did not agree to have their identifiable images included in the home meal video
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

05

Study design

Observational model
Ecologic or community
Time perspective
Prospective
Enrollment
100 participants (estimated)
Patient registry
No

Interventions

  • BehavioralMobile behavioral health

    The Wear-IT app will deliver intervention messages and information about healthy eating behaviors and information to participants own mobile devices regardless of connectivity.

06

What researchers measure

Primary outcomes

  1. Intervention Acceptability

    The Acceptability of Intervention Measure will assess the acceptability of the intervention. No summary score/scoring available. Range from Completely disagree to completely agree.

    Time frame: immediately after the 3-week intervention period

  2. Intervention Appropriateness

    The Intervention Appropriateness Measure will asses the appropriateness of the intervention. No summary score/scoring available. Range from Completely disagree to completely agree.

    Time frame: immediately after the 3-week intervention period

  3. Intervention Satisfaction

    The Satisfaction Survey will assess the participants' satisfaction with the intervention. Scored from 1 (Not at all) to 5 (Absolutely).

    Time frame: immediately after the 3-week intervention period

  4. Intervention Feasibility

    The Feasibility of Intervention Measure will assess participants' perception of the feasibility of this type of intervention. No summary score/scoring available. Range from Completely disagree to completely agree.

    Time frame: immediately after the 3-week intervention period

  5. Daily appropriateness of messages

    Ecological momentary assessment surveys will be completed daily to assess the appropriateness of each intervention message received that day. No summary score/scoring available. Range from Completely disagree to completely agree.

    Time frame: end of each intervention day at time chosen by participant

Other outcomes

  1. Home Food Environment

    Fulkerson Home Food Environment survey will be complete weekly for the 3 weeks of the study to assess types of food available in the home

    Time frame: Once each week of the 3-week intervention period on a day chosen by parents

  2. Child Eating Behaviors

    Video recordings of children eating at home will be coded to extract various child eating behavior metrics such as bite rate.

    Time frame: Once each week of the 3-week intervention period on a day chosen by parents

  3. Home Meal Information

    As part of a daily EMA surveys, parent will report on home meal environments and participants in home meals.

    Time frame: end of day after receipt of intervention messaging throughout the day

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: Yes

Supporting information: Study protocol, Analytic code

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Nov 2026; primary completion for May 2028, 18 months later.

Of 100 non-industry observational studies under Feeding Behavior, half reached primary completion within 25 months of starting (the median), counting those still running; a quarter within 9 and three quarters within 62. This study's planned 18 months is below that.

Counting every sponsor, half of 101 studies reached it within 24 months; a quarter within 8 and three quarters within 62.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 16, 2026
First posted
Nov 13, 2026
StartEst.
Nov 2026
Primary completionEst.
May 2028
CompletionEst.
May 2029
Last update
Nov 13, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Nov 13, 2026
Show all 1 update
  1. Nov 13, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07937033
Responsible party
Alaina Pearce (Principal Investigator, Penn State University) — Principal investigator
First posted
Nov 13, 2026
Start date
Nov 2026 (estimated)
Primary completion
May 2028 (estimated)
Completion
May 2029 (estimated)
Last update
Nov 13, 2026

Study contacts

Alaina Pearce, PhD
Contact
azp271@psu.edu
814-863-2120

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Nov 2026. You cannot join it, but the record below documents what was studied.

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Discussion

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