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Use of Video Consultation in Follow-up Care for Patients With a Neuroendocrine Tumor: a Feasibility Study

Use of Video Consultation in Follow-up Care for Patients With a NeuroEndocrine Tumor: a Feasibility Study (VIDEO-NET Study)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02147106
Acronym
VIDEO-NET
Enrollment
26
Registered
2014-05-26
Start date
2014-05-31
Completion date
2017-03-31
Last updated
2024-05-06

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

Conditions

Neuroendocrine Tumor

Keywords

Neuroendocrine tumor, Videoconsultation, Feasibility

Brief summary

Rationale: Patients with neuroendocrine tumors (NET) have a rare disease. Due to treating patients with a neuroendocrine tumor in 'NET knowledge centers' patients often have to travel long distances for follow-up visits at the outpatient clinic. Patients whose medical condition allows videoconsultation could save time by replacing outpatient clinic visits through videoconsultation for receiving follow-up care. Therefore, in this study we aim to introduce videoconsultation as a alternative for follow-up outpatient clinic visits in NET patients. Objective: The primary objective is to assess if use of videoconsultation in follow-up care for NET patients is feasible. We hypothesize that videoconsultation is a suitable medium for providing follow-up care in NET patients. Secondary objectives are to explore the amount of time videoconsultation takes in comparison with outpatient clinic visits and the acceptability and satisfaction of physicians and patients with using videoconsultation in follow-up care. Study design: The present study is a single-centre prospective feasibility study. Study population: Adult NET patients under surveillance or treatment of the department Medical Oncology at the University Medical Centre Groningen (UMCG) whose medical condition allows videoconsultation will be invited to participate. Intervention: Patient who give informed consent will participate in the study. Participants will receive follow-up care through videoconsultation instead of conventional visits at the outpatient clinic. Main study parameters/endpoints: The main endpoint is the feasibility of videoconsultation for follow-up care in NET patients. We hypothesize that videoconsultation is a suitable medium for providing follow-up care.

Interventions

Sponsors

University Medical Center Groningen
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Signed informed consent * Age ≥ 18 yrs * Grade I or II (low and intermediate grade) NET with any primary tumor type or disease stage * Have access to required equipment/technology for performing videoconsultation

Exclusion criteria

* Newly referred NET patients, who are visiting the department of Medical Oncology at the UMCG for the first time * Recently diagnosed NET patients, who are in the diagnostic phase of the disease * NET patients who frequently require blood tests, consultation or physical examination * A hearing or visual impairment, which would make videoconsultation difficult

Design outcomes

Primary

MeasureTime frameDescription
Feasibility1 yearParticipation rates, reason for declining participation, number of completed videoconsultations, dropout rate and reason for dropout will be noted in study records to evaluate feasibility of videoconsultation

Secondary

MeasureTime frameDescription
Amount of time1 yearThe amount of time NET patients are spending with videoconsultation in comparison with conventional outpatient clinic visits.
Acceptability and satisfaction of patients1 yearThe acceptability and satisfaction of patients with the use of videoconsultation will be assessed with a questionnaire and open-ended questions.
Acceptability and satisfaction of physicians1 yearThe acceptability and satisfaction of physicians with the use of videoconsultation will be assessed with a questionnaire and open-ended questions.

Countries

Netherlands

Outcome results

None listed

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