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Ostomy Belt Use Associated Quality of Life

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University of Miami

Status

Completed

Conditions

Stoma Colostomy
Stoma Ileostomy

Treatments

Other: Ostomy belt

Study type

Interventional

Funder types

Other

Identifiers

NCT04715893
20201333

Details and patient eligibility

About

The objective of this study is to elucidate whether the use of an ostomy belt can improve the quality of life in patients with an ostomy.

Enrollment

40 patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Current patients at University of Miami Hospital with stoma willing to trial an ostomy belt
  • 18 - 70 years old
  • Willing and able to sign informed consent

Exclusion criteria

  • Patients without stoma or unwilling to wear ostomy belt.
  • Have any condition that, in the opinion of the investigator, would compromise the well-being of the patient or the study or prevent the patient from meeting or performing study requirements.

Trial design

Primary purpose

Supportive Care

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

40 participants in 1 patient group

Ostomy belt group
Experimental group
Description:
Participants in this group will receive ostomy belts for eight weeks.
Treatment:
Other: Ostomy belt

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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