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Experiences and Needs of Patients, Their Informal Caregiver and Healthcare Professionals Regarding LARS

Rectal Cancer Survivorship, the Struggle of the Low Anterior Resection Syndrome (LARS). Experiences and Needs of Patients, Their Informal Caregiver and Healthcare Professionals

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04896879
Enrollment
69
Registered
2021-05-21
Start date
2016-11-22
Completion date
2020-12-31
Last updated
2021-05-21

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

Conditions

Low Anterior Resection Syndrome, Rectal Cancer

Keywords

low anterior resection syndrome

Brief summary

Exploration of the experiences and needs of patients with the low anterior resection syndrome, their informal caregiver and health care professionals. This is a qualitative study where semi-structured interviews will be conducted with patients and informal caregivers. next to that focus groups will be performed with healthcare professionals from different professions.

Interventions

BEHAVIORALinterviews

semi-structured interviews will be conducted in patients with major LARS and their informal caregiver to explore their experiences and needs. Focus groups will be perfomed with healthcare professionals of several professions.

Sponsors

Kom Op Tegen Kanker
CollaboratorOTHER
AZ Sint-Jan AV
CollaboratorOTHER
AZ Delta
CollaboratorOTHER
AZ Sint-Lucas Gent
CollaboratorOTHER
University Hospital, Ghent
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

PATIENTS Inclusion Criteria: * adult patients (18+) * confronted with major low anterior resection syndrome after rectal cancer surgery

Exclusion criteria

* stoma at time interview * abdominal perineal resection INFORMAL CAREGIVERS Inclusion criteria * Adults (18+) * Nominated by the participating patient as their principal caregiver

Design outcomes

Primary

MeasureTime frameDescription
needs and experiences of patients with major lars and their informal caregiver through individual semistructered interviewsInterview will last about 60 minutesExploring needs and experiences of patients with major lars and their informal caregiver through individual semistructured interviews
Needs and experiences of healthcare professionals caring for patients with LARS through focus groupsFocus group will last about 60 minutesExploring needs and experiences of healthcare professionals caring for patients with LARS

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 12, 2026