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Weighted Blanket to Treat Anxiety Related to Trying New Foods the Pediatric Population (Food Anxiety)

The University of Texas System (UT) logo

The University of Texas System (UT)

Status

Terminated

Conditions

Avoidant Restrictive Food Intake Disorder
Food Neophobia
Picky Eating
Anxiety State

Treatments

Device: weighted blanket

Study type

Interventional

Funder types

Other

Identifiers

NCT06420232
23-0342

Details and patient eligibility

About

This small experimental pilot study addresses the knowledge gap related to the use of weighted blankets for children with anxiety related to food and eating.

Full description

The purpose of the study is to research if weighted blankets might help children with anxiety related to food tolerate new foods better. The parent will be asked to complete a 10-question questionnaire and make a list of the foods the child eats on three occasions (before the study begins, after a control period and after the child uses the weighted blanket). The child will be asked to use a weighted blanket for 5 to 15 minutes prior to at least 3 meals a week for one month, and the child will be asked to complete a 20-question questionnaire taking about 5-12 minutes to complete asking about how they feel on days that they use the weighted blanket and one time a week during the month that they don't use the weighted blanket. The parent will be asked to report any new foods the child tries on the days that they do use the weighted blanket. The parent will be asked to keep the weighted blanket and supervise all use of the weighted blanket for safety. This study will take approximately 2 months total.

Enrollment

6 patients

Sex

All

Ages

8 to 12 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Subject and guardian has provided informed consent in a manner approved by the IRB and is willing and able to comply with the trial procedures.
  2. Subject has identified feeding challenges
  3. Subject has anxiety related to food as reported by caregiver
  4. Subject is between the ages of 8-12
  5. Subject has good reading abilities
  6. Subject weighs 30 pounds or more

Exclusion criteria

  1. Any medical condition that, in the opinion of the investigator, would place the subject at increased risk for participation due to the inability to remove the blanket safely. Examples of diagnoses that would exclude a participant include spinal cord injury, cerebral palsy, and muscular dystrophy.
  2. Concurrent participation on another research study
  3. Participants outside of the ages 8-12
  4. Participants refuse to use the weighted blanket
  5. If the use of a weighted blanket is contraindicated for any reason
  6. Participants lacking the reading ability to complete a questionnaire
  7. Participants who weigh under 30 pounds per parent report and cannot use a commercially available weighted blanket as the minimum weight of a weighted blanket is 3 pounds will be excluded but this exclusion is unlikely due to the inclusion age range

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

6 participants in 1 patient group

Weighted Blanket
Experimental group
Treatment:
Device: weighted blanket

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Heather D Celkis, BS; Claudia A Hilton, PhD

Data sourced from clinicaltrials.gov

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