Focus Group Interviews of Patients With Permanent or Temporary Enterostomas
NCT ID: NCT01156506
Last Updated: 2012-12-12
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
22 participants
OBSERVATIONAL
2010-02-28
2010-04-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
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
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
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
See the medical conditions and disease areas that this research is targeting or investigating.
Keywords
Explore important study keywords that can help with search, categorization, and topic discovery.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Patients with permanent enterostoma due to other causes.
* Patients with temporary ileostomy.
Exclusion Criteria
* Patients who do not communicate in Danish.
* Patients with severe hearing impairment.
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Herlev Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Anne Kjærgaard Danielsen
Ph.d.student, RN
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Anne K. Danielsen, Nurse, MaClN
Role: PRINCIPAL_INVESTIGATOR
Herlev University Hospital, department of surgery
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
AKD02
Identifier Type: -
Identifier Source: org_study_id