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The Impact Of A Patient Support Community On Patients With Neuroendocrine Cervical Cancer: NECC Peer Support

The Impact Of A Patient Support Community On Patients With Neuroendocrine Cervical Cancer: NECC Peer Support

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07532954
Enrollment
40
Registered
2026-04-16
Start date
2026-04-13
Completion date
2028-11-01
Last updated
2026-05-18

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

Conditions

Neuroendocrine Cervical Cancer, Patient Support

Brief summary

To learn about the effects of a participant support community on illness perception, emotional well-being, and feelings of isolation among participants with NECC.

Detailed description

Primary Objective 1\. To assess the impact of a participant support community on illness perception, emotional wellbeing and feelings of isolation among participants diagnosed with NECC. Secondary Objectives 1. To understand how peer support affects communication with healthcare providers. 2. To explore how the support community affects coping strategies. 3. To evaluate the perceived value and acceptability of the support community structure and delivery. 4. To identify unmet needs and challenges experienced by participants with NECC.

Interventions

OTHERQuestionnaire

Demographic questionnaire

Sponsors

M.D. Anderson Cancer Center
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

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

Inclusion criteria

Eligibility Criteria * Histologically confirmed NECC. * Aged 18 years or older. * English proficient. * Provision of signed and dated informed consent form. * Stated willingness to comply with all study procedures and availability for the duration of the study. * Access to necessary resources for participating in a technology-based intervention (i.e., computer, smartphone, internet access).

Exclusion criteria

None

Design outcomes

Primary

MeasureTime frameDescription
Demographic questionnaireThrough study completion; an average of 1 yearThis questionnaire will collect basic information including age, marital status, number of children, disease stage at diagnosis, and current disease status and treatment.

Countries

United States

Contacts

CONTACTLarissa Meyer, MD
lmeyer@mdanderson.orgMeyer
PRINCIPAL_INVESTIGATORLarissa Meyer, MD

M.D. Anderson Cancer Center

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 19, 2026