Living With a Parastomal Bulge - a Phenomenological-hermeneutic Study of Patients Lived Experiences

Sponsor
Rigshospitalet, Denmark (Other)
Overall Status
Completed
CT.gov ID
NCT02889536
Collaborator
Herlev Hospital (Other)
20
1
4
5

Study Details

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Focus group interviews

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)

Study Design

Study Type:
Observational
Actual Enrollment :
20 participants
Official Title:
Living With a Parastomal Bulge - a Phenomenological-hermeneutic Study of Patients Lived Experiences
Study Start Date :
Jun 1, 2016
Actual Primary Completion Date :
Oct 1, 2016
Actual Study Completion Date :
Oct 1, 2016

Arms and Interventions

Arm Intervention/Treatment
Focus group interview, stoma clinics

Qualitative data collection. Patients attending stoma clinics in the capital region

Other: 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 Names:
  • Qualitative data collection
  • Focus group interview, referred

    Qualitative data collection. Patients referred to repair surgery at a specific hospital in the capital region

    Other: 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 Names:
  • Qualitative data collection
  • Outcome Measures

    Primary Outcome Measures

    1. Patients' experiences of symptoms in relation to parastomal bulging and the impact on everyday life [1 day]

      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

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    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

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Marianne Krogsgaard Copenhagen Denmark 2100

    Sponsors and Collaborators

    • Rigshospitalet, Denmark
    • Herlev Hospital

    Investigators

    • Study Chair: Thordis Thomsen, PhD, RN, Abdominal Centre, Rigshospitalet, Copenhagen Denmark

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Marianne Krogsgaard, RN, MHS, Rigshospitalet, Denmark
    ClinicalTrials.gov Identifier:
    NCT02889536
    Other Study ID Numbers:
    • PreParE-qualitative
    First Posted:
    Sep 5, 2016
    Last Update Posted:
    Oct 21, 2016
    Last Verified:
    Oct 1, 2016
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Keywords provided by Marianne Krogsgaard, RN, MHS, Rigshospitalet, Denmark
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 21, 2016