Living With a Parastomal Bulge - a Phenomenological-hermeneutic Study of Patients Lived Experiences
NCT ID: NCT02889536
Last Updated: 2016-10-21
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
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COMPLETED
20 participants
OBSERVATIONAL
2016-06-30
2016-10-31
Brief Summary
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Detailed Description
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A bulge may be relatively obvious or extremely difficult to diagnose. Most parastomal bulging occurs within two years of stoma formation but is seen up to 20 years post-surgery. Despite advances in primary surgical and repair techniques a rising incidence of parastomal bulging is expected in the future due to increased survival of cancer patients with an ostomy and limited dissemination of new techniques. Approximately one in three patients with a parastomal hernia requires a surgical hernia repair. However, the majority of patients are referred to non-surgical treatment by the enterostomal therapist in the outpatient clinic or do not seek professional help to manage the bulge. Previous studies report that quality of life as well as physical, psychological and social function are affected in patients with parastomal bulging.
Descriptions of symptoms vary from 'asymptomatic', 'symptomatic' to 'high symptom load'. Most frequently reported symptoms include ostomy leakage, skin problems, difficulty with ostomy appliance, limitation of activity, difficulty with clothing, cosmetic complaints, social restriction, erratic action of the stoma and a bearing down sensation at the site of the stoma. Rare, but serious complications include complete obstruction, strangulation or incarceration. However, there is a lack of knowledge of patients' lived experiences with parastomal bulging. Insight into patients' experiences of symptoms in relation to parastomal bulging and the impact on everyday life may help identify issues of importance from the patient perspective. This, in turn, may help professionals to better understand and support patients with PB, and be of help when identifying patients' symptoms and determining relevant treatment strategies.
Purpose: The aim is to study stoma patients experiences of parastomal bulging and symptoms in everyday life (in relation to an ileostomy and colostomy)
Conditions
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Study Groups
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Focus group interview, stoma clinics
Qualitative data collection. Patients attending stoma clinics in the capital region
Focus group interviews
Focus group interviews. Two groups with patients referred to repair of parastomal bulging and three groups with patients attending the outpatient stoma clinics
Focus group interview, referred
Qualitative data collection. Patients referred to repair surgery at a specific hospital in the capital region
Focus group interviews
Focus group interviews. Two groups with patients referred to repair of parastomal bulging and three groups with patients attending the outpatient stoma clinics
Interventions
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Focus group interviews
Focus group interviews. Two groups with patients referred to repair of parastomal bulging and three groups with patients attending the outpatient stoma clinics
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
PB diagnosed by stoma care nurse
Ability to speak and understand Danish
Exclusion Criteria
Major incisional abdominal hernias
18 Years
ALL
No
Sponsors
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Herlev Hospital
OTHER
Rigshospitalet, Denmark
OTHER
Responsible Party
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Marianne Krogsgaard
RN, MHS
Principal Investigators
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Thordis Thomsen, PhD, RN
Role: STUDY_CHAIR
Abdominal Centre, Rigshospitalet, Copenhagen Denmark
Locations
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Marianne Krogsgaard
Copenhagen, Copenhagen, Denmark
Countries
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Other Identifiers
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PreParE-qualitative
Identifier Type: -
Identifier Source: org_study_id
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