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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03840720
Other study ID # PR-1.0
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 1, 2019
Est. completion date December 31, 2019

Study information

Verified date April 2020
Source Vastra Gotaland Region
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

"The patient's journey" is an interview based study assessing the patients' experience from the first symptoms to a final diagnosis focusing on patients with small intestinal neuroendocrine tumors.


Description:

The project focus on patients with small intestinal neuroendocrine tumors (SiNET's) with an incidence of 1-2/100 000 yearly. The primary tumor(s) are often small and symptoms usually arise when the disease has become metastatic with hormonal symptoms and/or symptoms due to local growth. As the tumors grow slowly and the symptoms in many cases are rather diffuse and develops gradually over a long time period there is often a long delay from onset to a final diagnosis both depending on "patient's delay" and "doctor's delay" The aim of the current project is to map and analyze the patient's journey from the first appearance of symptoms to the time point of a final diagnosis and to try to identify factors contributing to a delayed process.

The method is interview based and the interviews will be analyzed through the Design Thinking Methodology


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date December 31, 2019
Est. primary completion date July 31, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients living in Western Sweden

- > 18 years of age

- Performance status 0-3

- Expected remaining survival of > 6 months

- Diagnosed with a small intestinal neuroendocrine tumor during 2016-2018

Exclusion Criteria:

- Not able to read and/or understand Swedish language

- Dementia/memory loss

- Performance status >3

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Sweden Dept of Oncology Gothenburg

Sponsors (2)

Lead Sponsor Collaborator
Vastra Gotaland Region Novartis

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary Initial symptoms Mapping of patients initial symptoms and their time points through indepths interviews by design thinking methodology October 2019
Primary Health care actions Mapping of corresponding health care actions and their time points regarding the investigations of symptoms October 2019
Primary Reasons for a delayed diagnosis Mapping of herdles and delays in reaching a final diagnosis through design thinking methodology analysing the patients symptoms and the corresponding Health care actions October 2019
Secondary Patients' efforts Mapping of actions taken by the patient, trying to be diagnosed correctly, through indepths interviews by design thinking methodology October 2019
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