Focus Group Interviews of Patients With Permanent or Temporary Enterostomas

NCT ID: NCT01156506

Last Updated: 2012-12-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

22 participants

Study Classification

OBSERVATIONAL

Study Start Date

2010-02-28

Study Completion Date

2010-04-30

Brief Summary

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The study seeks to gain knowledge about new and of alternative ways of organizing ostomy training based on informants' own experiences of life with a stoma.

The study is designed and conducted as qualitative focus group interviews with three different groups of patients with enterostomas (5-8 in each group): a) people with permanent enterostoma due to cancer, 2) people with permanent enterostoma due to non-cancer and 3) people with a temporary ileostomy.

Detailed Description

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The study is investigating the perspective of the patients who have actually experienced having surgery and living with an enterostoma.

By applying this method it is possible to gain access and in depth knowledge of complex issues including sensitive data. The dialogue with peers can lead to experiments and associations which might stimulate the informants to produce new insights within the individual and in the group.

The interviews will be transcribed in full and analyzed with qualitative content analysis with a phenomenological and hermeneutical approach

Conditions

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Patient Perspective Living With an Enterostoma Mastery Empowerment

Keywords

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focus group interview quality of life patient education rehabilitation

Eligibility Criteria

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Inclusion Criteria

* Patients with permanent enterostoma due to cancer.
* Patients with permanent enterostoma due to other causes.
* Patients with temporary ileostomy.

Exclusion Criteria

* Patients with severe mental disorders.
* Patients who do not communicate in Danish.
* Patients with severe hearing impairment.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Herlev Hospital

OTHER

Sponsor Role lead

Responsible Party

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Anne Kjærgaard Danielsen

Ph.d.student, RN

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Anne K. Danielsen, Nurse, MaClN

Role: PRINCIPAL_INVESTIGATOR

Herlev University Hospital, department of surgery

Other Identifiers

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AKD02

Identifier Type: -

Identifier Source: org_study_id