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Clinical Trials/NCT05457660
NCT05457660UnknownNot Applicable

Transverse Study About QOL for Colostomized or Ileostomized Patients During Their Home Hospitalization

Fondation Sante Service1 site in 1 country100 target enrollmentStarted: February 15, 2022Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Sponsor
Enrollment
100
Locations
1
Primary Endpoint
Measuring the quality of life of colostomized or ileostomized patients in home hospitalization

Study Overview

Brief Summary

The goalf of the study is to have a basis about QOL for colo-stoma and ileo-stoma for patients which are hospitalized at home. The QOL measurement is done with a questionnaire of several items made by stomatherapist and also using EQ5D QOL form.

After reviewing of the data, our goal is to create or improve some solutions to improve their QOL during their home hospitalization.

Study Design

Study Type
Observational
Observational Model
Other
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 99 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Colo-stomy or Ileo-stomy patient
  • Patient hospitalized at home by Fondation Sante Service (Fr)
  • 18 YO or more
  • Non-opposition to the study

Exclusion Criteria

  • Patient not able to read or properly understand the Information Consent Form and not able to complete the questionnaire for any reason.

Outcomes

Primary Outcomes

Measuring the quality of life of colostomized or ileostomized patients in home hospitalization

Time Frame: 4 months

Secondary Outcomes

  • Identify patient issues and needs.(4 months)
  • Analyze the results by subgroups of patients: according to the type of stoma (ileostomy vs. colostomy; temporary stomy vs. permanent stoma), age of the stoma, age, pathology.(4 months)

Investigators

Sponsor
Fondation Sante Service
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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