The Impact Of A Patient Support Community On Patients With Neuroendocrine Cervical Cancer: NECC Peer Support
Neuroendocrine Cervical Cancer · Patient Support
What this study involves
The registry says this study is recruiting. Individual locations may have different availability.
- Study type
- Observational
- Phase
- Not applicable / not listed
- Age range
- 18 years - Not specified
- Sex eligible
- All sexes
- Healthy volunteers
- Not accepted
- Participants
- 40 Estimated
These are starting points, not an eligibility decision. The research team must review the full requirements.
About the research
To learn about the effects of a participant support community on illness perception, emotional well-being, and feelings of isolation among participants with NECC.
Read the full 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.
Who may be able to participate?
The list below is the sponsor’s full registry wording. It can include conditions, prior treatment, test results and other requirements. A match in search does not mean you qualify.
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
Study population
MD Anderson Cancer Center
Understand screeningTreatment, groups and participation
The registry may describe treatments and study duration without a complete visit calendar. Ask the study team for the exact schedule, procedures, risks, costs and alternatives. Keep your usual care plan unless your treating clinician tells you otherwise.
- Assignment
- Not reported
- Masking
- Not reported
Focus Group
participants will take part in a focus group session to share their personal experiences
Other: Questionnaire
Questionnaire OTHER
Demographic questionnaire
What researchers are measuring
Outcome measures describe what is being studied. They are not proof that a treatment works.
Primary measures
Demographic questionnaire
Time frame: Through study completion; an average of 1 year
This questionnaire will collect basic information including age, marital status, number of children, disease stage at diagnosis, and current disease status and treatment.
Review the complete result tables and limitations in the official record.
Open official results ↗Research locations (1)
The overall study status and a local site’s status can differ. Confirm that location’s availability before traveling.
1 locations
MD Anderson Cancer CenterHouston, Texas, United StatesRecruiting
Study team and timeline
- Lead sponsor
- M.D. Anderson Cancer Center
- Study start
- Apr 13, 2026 Actual
- Primary completion
- Nov 1, 2028 Estimated
- Study completion
- Nov 1, 2028 Estimated
- First posted
- Apr 16, 2026 Actual
- Last updated
- Nov 10, 2026 Actual
Official study contacts
Official study title
The Impact Of A Patient Support Community On Patients With Neuroendocrine Cervical Cancer: NECC Peer Support
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Source: ClinicalTrials.gov API v2. Information is submitted by sponsors and investigators. NLM does not approve the safety or science of all listed studies. Registry disclaimer.
Retrieved: Nov 12, 2026 · Last registry update: Nov 10, 2026