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Acceptability and Efficacy of the Zemedy App for Irritable Bowel Syndrome

University of Pennsylvania logo

University of Pennsylvania

Status

Completed

Conditions

Irritable Bowel Syndrome

Treatments

Behavioral: Zemedy App for Irritable Bowel Syndrome

Study type

Interventional

Funder types

Other
Industry

Identifiers

Details and patient eligibility

About

The purpose of this research is to assess if a new self-help app for IBS is an acceptable and effective intervention for improving the overall quality of life in patients with Irritable Bowel Syndrome.

Enrollment

146 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosis of IBS. Own a smart phone. Speak English

Exclusion criteria

  • Under age of consent (18) Diagnosed with another GI disorder (e.g. celiac disease, inflammatory bowel disease)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

146 participants in 2 patient groups

Immediate Treatment
Experimental group
Description:
Participants will have immediate access to the self-help app. They will take 8 weeks to work through the content at their own pace.
Treatment:
Behavioral: Zemedy App for Irritable Bowel Syndrome
Waitlist Control
No Intervention group
Description:
Participants in the waitlist will receive no intervention for 8 weeks, other than a few "check in" emails from study personnel. At the end of 8 weeks, they will be crossed over to the active treatment group and will be given access to the app.

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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