Living With a Parastomal Bulge - a Phenomenological-hermeneutic Study of Patients Lived Experiences
Primary Purpose
Ostomy, Hernia, Signs and Symptoms
Status
Completed
Phase
Locations
Denmark
Study Type
Observational
Intervention
Focus group interviews
Sponsored by
About this trial
This is an observational trial for Ostomy focused on measuring parastomal hernia, ostomy, qualitative, phenomenological-hermeneutic research, symptoms, parastomal bulging
Eligibility Criteria
Inclusion Criteria:
Permanent or temporary active sigmoidostomy, transversostomy, jejunostomy or ileostomy
PB diagnosed by stoma care nurse
Ability to speak and understand Danish
Exclusion Criteria:
Previous surgical repair for PB
Major incisional abdominal hernias
Sites / Locations
- Marianne Krogsgaard
Arms of the Study
Arm 1
Arm 2
Arm Type
Arm Label
Focus group interview, stoma clinics
Focus group interview, referred
Arm Description
Qualitative data collection. Patients attending stoma clinics in the capital region
Qualitative data collection. Patients referred to repair surgery at a specific hospital in the capital region
Outcomes
Primary Outcome Measures
Patients' experiences of symptoms in relation to parastomal bulging and the impact on everyday life
A funnel-based interview approach will be used, allowing for a less structured, open beginning moving to a more structured ending ensuring that the research question will be answered
Secondary Outcome Measures
Full Information
NCT ID
NCT02889536
First Posted
August 30, 2016
Last Updated
October 20, 2016
Sponsor
Rigshospitalet, Denmark
Collaborators
Herlev Hospital
1. Study Identification
Unique Protocol Identification Number
NCT02889536
Brief Title
Living With a Parastomal Bulge - a Phenomenological-hermeneutic Study of Patients Lived Experiences
Official Title
Living With a Parastomal Bulge - a Phenomenological-hermeneutic Study of Patients Lived Experiences
Study Type
Observational
2. Study Status
Record Verification Date
October 2016
Overall Recruitment Status
Completed
Study Start Date
June 2016 (undefined)
Primary Completion Date
October 2016 (Actual)
Study Completion Date
October 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rigshospitalet, Denmark
Collaborators
Herlev Hospital
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
A parastomal bulge (PB) is a frequent long-term complication after stoma formation. Most parastomal bulging occurs within two years of stoma formation but is seen up to 20 years post-surgery. A bulge may be relatively obvious or extremely difficult to diagnose, and descriptions of symptoms vary from 'asymptomatic', 'symptomatic' to 'high symptom load'. Previous studies report that quality of life as well as physical, psychological and social function are affected in patients with parastomal bulging. 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.
Detailed Description
Stoma formation is a commonly performed procedure in colorectal surgery as part of treatment for malignant- and inflammatory bowel disease. A parastomal bulge (PB) is a frequent long-term complication with an incidence varying from 4% to more than 40% depending on ostomy type, follow-up and definitions.
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)
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ostomy, Hernia, Signs and Symptoms
Keywords
parastomal hernia, ostomy, qualitative, phenomenological-hermeneutic research, symptoms, parastomal bulging
7. Study Design
Enrollment
20 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Focus group interview, stoma clinics
Arm Description
Qualitative data collection. Patients attending stoma clinics in the capital region
Arm Title
Focus group interview, referred
Arm Description
Qualitative data collection. Patients referred to repair surgery at a specific hospital in the capital region
Intervention Type
Other
Intervention Name(s)
Focus group interviews
Other Intervention Name(s)
Qualitative data collection
Intervention Description
Focus group interviews. Two groups with patients referred to repair of parastomal bulging and three groups with patients attending the outpatient stoma clinics
Primary Outcome Measure Information:
Title
Patients' experiences of symptoms in relation to parastomal bulging and the impact on everyday life
Description
A funnel-based interview approach will be used, allowing for a less structured, open beginning moving to a more structured ending ensuring that the research question will be answered
Time Frame
1 day
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Permanent or temporary active sigmoidostomy, transversostomy, jejunostomy or ileostomy
PB diagnosed by stoma care nurse
Ability to speak and understand Danish
Exclusion Criteria:
Previous surgical repair for PB
Major incisional abdominal hernias
Study Population Description
Stoma patients that are routinely followed for at least one year post surgery by stoma care nurses (SCNs) at the outpatient stoma clinics at the five hospitals within the region.
Sampling Method
Non-Probability Sample
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Thordis Thomsen, PhD, RN
Organizational Affiliation
Abdominal Centre, Rigshospitalet, Copenhagen Denmark
Official's Role
Study Chair
Facility Information:
Facility Name
Marianne Krogsgaard
City
Copenhagen
ZIP/Postal Code
2100
Country
Denmark
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Living With a Parastomal Bulge - a Phenomenological-hermeneutic Study of Patients Lived Experiences
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