Perception of Needs of Patients With Chronic Intestinal Failure and Their Practitioners: a Qualitative Study

Qualitative Assessment of the Needs and Knowledge of Patients With Chronic Intestinal Failure of Their Disease as Well as Those of Their Practitioners

Status

UNKNOWN

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT04390633

Acronym

SBS-NEEDS

Enrollment

Registered

2020-05-15

Start date

2020-10-01

Completion date

2022-12-31

Last updated

2020-07-21

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

Conditions

Chronic Intestinal Failure, Small Intestine Disease

Brief summary

The SBS NEEDS Study is a qualitative transversal study aiming to describe and understand the needs and knowledge of patients with Chronic Intestinal Failure as well as the representations of their practitioners Chronic Intestinal Failure (CIF) is the long-lasting reduction of gut function, below the minimum necessary for the absorption of macronutrients and/or water and electrolytes, such that intravenous supplementation is required to maintain health and/or growth. CIF is the rarest organ failure. Home parenteral nutrition (HPN) is the primary treatment for CIF. Semi-structured interviews will be conducted with patients in two nutrition unit and specialized in the small bowel diseases in two French region. 20 situations will be included. After analysing the data of the individual interviews, focus groups will be conducted with health professionals from an accredited home parenteral nutrition department.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

CROSS_SECTIONAL

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* Men and women aged 18 and over * With Chronic Intestinal Failure (CIF) : reduction of the intestinal functional mass below the minimum mass sufficient to ensure the absorption of nutrients to maintain nutritional status * medical follow-up in one of the two nutrition departments of the study * Informed consent stating that the subject understood the purpose and methodology of the study and agrees to participate in the study.

Exclusion criteria

* Persons with proven and significant cognitive impairment preventing the completion of semi-structured interviews * Person who does not speak French easily * Generally, any person unlikely to cooperate in the study * Adults under guardianship

Design outcomes

Primary

Measure	Time frame	Description
20 semi-structured interviews	12 months	Qualitative data analysis - Theorical saturation

Outcome results