A Study to Collect the Somatuline® Injector Device Preferences of Patients Living With Neuroendocrine Tumor (NET) and Nurses Involved in the Care of Patients With NET

Ipsen

Status: Terminated

Conditions: Neuroendocrine Tumors

Study type: Observational

Funder types: Industry

Identifiers

NCT05922579

CLIN-52030-458

Details and patient eligibility

About

This study aims to investigate the treatment preferences of patients with Neuroendocrine Tumors (NETS) and nurses who are involved in the care of individuals with NETs. NETs are a type of abnormal growth that can develop in various parts of the body, such as the lungs, pancreas, gastrointestinal tract, or other organs.

NETs originate from specialized cells called neuroendocrine cells, which are responsible for producing hormones in our bodies.

The study focuses on hypothetical preferences regarding the use of two different type of devices for administering Somatostatin analogues (SSAs), which could be used in the treatment of NETs.

SSAs work by imitating the actions of a hormone called somatostatin that naturally exists in our bodies. These treatment help to control the symptoms of NETs by blocking the release of hormones from the tumor cells.

The devices under consideration are a motorized injector versus a manual injector.

Participants in the study will be asked to take part in:

1. An interview based on a draft survey: 60-minute interview over videocall, to examine participants understanding of the online survey; or
2. Final online survey: 30-minute online survey. This involves presenting patients and nurses with different treatment options and asking them to choose their preferred option.

By analysing the choices made by participants, researchers can understand which attributes of the injector devices are most important to patients and nurses.

Individual participation is limited to the interview based on a draft survey (60 minutes) or the final online survey (30 minutes).

No further participation is required beyond this.

Enrollment: 191 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

Patients (cognitive interviews)

• Aged 18 years or over
• Reside in the US or Canada
• Have been diagnosed with NETs by a healthcare professional (based on self-report and confirmed via data quality checks)
• Have any SSA treatment experience in the past 2 years
• Be fluent in spoken and written English
• Have read, understood, and consented to participate in the study
• Be able to complete the survey on a standard-sized tablet device (minimum 10 inches), laptop, or desktop computer
• Be able and willing to screenshare with the interviewer

Patients (online survey and DCE)

• Aged 18 years or over
• Reside in the US or Canada
• Have been diagnosed with NETs by a healthcare professional (based on self-report and confirmed via data quality checks)
• Have any SSA treatment experience in the past 2 years
• Be fluent in spoken and written English
• Have read, understood, and consented to participate in the study
• Be able to complete the survey on a standard-sized tablet device (minimum 10 inches), laptop, or desktop computer
• Have not participated in the cognitive interviews

Nurses (cognitive interviews)

• Reside in the US or Canada
• Nurse with at least 12 months experience caring for patients with NETs
• Have administered at least one long-acting SSA injection to a patient with NETs in the past 12 months
• Be fluent in spoken and written English
• Have read, understood, and consented to participate in the study
• Be able to complete the survey on a standard-sized tablet device (minimum 10 inches), laptop, or desktop computer
• Be able and willing to screenshare with the interviewer

Nurses (online survey and DCE)

• Reside in the US or Canada
• Nurse with at least 12 months experience caring for patients with NETs
• Have administered at least one long-acting SSA injection to a patient with NETs in the past 12 months
• Be fluent in spoken and written English or Canadian French
• Have read, understood, and consented to participate in the study
• Be able to complete the survey on a standard-sized tablet device (minimum 10 inches), laptop, or desktop computer
• Have not participated in the cognitive interviews

Exclusion criteria

• No access to internet