Skip to content

Quality of Life in Patients With and Without a Parastomal Bulge

Quality of Life in Patients With and Without a Parastomal Bulge - a Cross-sectional Study of Patients in the Danish Stoma Database Capital Region

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03702478
Enrollment
1453
Registered
2018-10-11
Start date
2018-08-13
Completion date
2018-12-31
Last updated
2019-04-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Parastomal Hernia, Quality of Life

Keywords

Quality of life, hernia, parastomal bulging, stoma, cross-sectional

Brief summary

It is not well-established whether a parastomal bulge impacts stoma patients HRQoL or if HRQOL differs according to the underlying disease or type of stoma. In this large cross-sectinal study stoma patients with and without a parastomal bulge are asked about their health-related quality of life and stomarelated quality of life. Stoma patients are identified in the danish stoma database and contacted two times by email. Non-responders are sent a paper booklet.

Detailed description

A cross-sectional study of patients registered in the Danish Stoma Database Capital Region (DSDCR), with permanent or temporary enterostoma after surgery performed between 2011 and 2016. Via a unique personal identification number registered in DSDCR patients will be contacted by e-mail using the e-Boks system, an official electronic distribution system covering around 80% of the Danish adult population. The e-mail will contain information about the study and a personal link to SurveyXact, an online survey program allowing for direct electronic data entry by patients. First reminder will be sent after one week and a second reminder again one week later. If necessary, a third reminder additionally three weeks later will be sent to patients by post, including a paper booklet of the questionnaires as described below. For patients without e-Boks, DSDCR will be linked to the Danish Civil Registration System via the unique personal identification number, providing information on patient's addresses. Information on the study and a paper booklet of questionnaires will be sent to patients by post. A reminder will be sent by post after three weeks if necessary. Hereafter, no further attempts will be made to contact the patients. To include other relevant variables in the analysis of data, data from the Danish Anaesthesia Database (DAD) and the Danish Colorectal Cancer Database will be linked. Quality of life will be assessed using StomaQol and SF-36. Colostomy Impact score will also be obtained. Patients will self-report a parastomal bulge and information such as education, alcohol consumption, physical activity and civil status.

Interventions

OTHERQuestionnaire

No intervention only observational

Sponsors

The Novo Nordic Foundation
CollaboratorOTHER
Herlev and Gentofte Hospital
CollaboratorOTHER
Rigshospitalet, Denmark
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 110 Years
Healthy volunteers
No

Inclusion criteria

* permanent active sigmoideostomy, transverseostomy, jejunostomi or ileostomy * temporary active sigmoideostomy, transverseostomy, jejunostomi or ileostomy

Exclusion criteria

* age younger than 18 years * stoma closure at follow-up * death

Design outcomes

Primary

MeasureTime frameDescription
Health related quality of life (SF-36 ) and Stoma related Qol (StomaQol) in relation to stoma type or underlying conditionUp to 7 years after stoma formationInvestigate and compare HRQoL in patients with and without a self-reported parastomal bulge in relation to an ileostomy or colostomy. HRQol is measured with SF-36 and StomaQol

Secondary

MeasureTime frameDescription
Relationship between symptoms and HRQOL measured with StomaQolUp to 7 years after stoma formationInvestigate the relationship between symptoms in the Stomaqol scale and overall score
Exploration of the frequency of self-reported parastomal bulgingUp to 7 years after stoma formationInvestigate the frequency of parastomal bulging
Relationship between PB duration and HRQOL measured with StomaQol and SF-36Up to 7 years after stoma formationThe association between duration of PB and overall scores on SF-36 and StomaQol
Relationship between PB size and HRQOL measured with SF-36 and StomaQolUp to 7 years after stoma formationThe association between duration of PB and overall scores on SF-36 and StomaQol

Other

MeasureTime frameDescription
Smoking measured by selfreported smoking status. A non-validated scaleUp to 7 years after stoma formationExploration of the distribution of smoking in stoma patients with and without parastomal bulging. Smoking status is categorised as never smoked, stopped smoking for \> 6 months, stopped smoking \< 6 months, smoking occationally, smoking every day. The category never smoked will be categorised as 'never smoker'. The categories stopped smoking \< or \> than 6 months ago will be categorised as 'previous smoker'. The categories smoking occationally and smoking every day will be categorised as 'current smokers'.
Physical activity measured with high or low intensity questions. A non-validated physical activity scaleUp to 7 years after stoma formation.Exploration of the distribution of high and low intensity physical activity in stoma patients with and without parastomal bulging. High intensity physical activity as for example running, playing football or tennis, measured in minutes (min.) pr week. Scale: 0 min, \<30 min., 30-59 min., 60-120 min. and \>120 min. Values \<30 min. or 0 min. is considered low physical activity of high-intensity. 30-59 min. is considered medium physical activity of high intensity. Values \> 60 min ia considered high physical activity level of high intensity. Low intensity physical activity as for example walking, doing the garden or cleaning the house, measured in minutes pr week. Scale: 0 min., \<30 min., 30-60 min., 61-90 min., 91-150 min., 151-300 min. and \>300 min. Values \<60 min is considered low physical activity of low intensity. Values from 61-150 is considered medium physical activity of low intensity. Values from 151 or more is considered high physical activity level of low intensity.
Alcohol consumption measured by Time-line-follow-backUp to 7 years after stoma formationExploration of the distribution of alcohol consumption in stoma patients with and without parastomal bulging.

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026