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NCT03776253Completed

Conquer Fear SUPPORT Intervention in Supporting Patients With Stage III-IV Lung or Gynecologic Cancer

Conquer Fear SUPPORT: A Psychosocial Intervention in Patients With Advanced Cancer

Source: ClinicalTrials.gov · Last updated 28 Oct 2026

Brief summary (registry, in English)

This trial will pilot a psychosocial intervention called Conquer Fear Support (CFS) in patients with stage III-IV lung or gynecologic cancer who are experiencing fear of cancer progression. The intervention is adapted from a novel program called "Conquer Fear" which was developed by researchers in Australia. CFS may help in reducing worries, fears, and uncertainty in patients with advanced lung or gynecological cancer.

Status (registry)
Completed
Study type
Interventional
Enrollment
39 (actual)
First submitted
31 Oct 2018
Start date
13 Nov 2018
Primary completion date
26 Jul 2024
Lead sponsor
City of Hope Medical Center
NCT number
NCT03776253

What you commit to

  • Study type: Interventional
  • Participants enrolled: 39
  • From 13 Nov 2018 to the primary completion date, 26 Jul 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients who are currently receiving ongoing psychiatric treatment

Other illness

  • Current severe depression or psychosis; significant cognitive impairment
  • Patients enrolled in hospice care or who opt to receive no further disease-focused treatment

Other

  • Non-English speaking

Who the study is looking for

  • Patients with gynecologic (GYN) and lung cancer will be recruited
  • Stage III or IV disease
  • At least 3 months from initial diagnosis
  • Receiving disease-focused treatment or active surveillance mode
  • A score of ≥ 34 on the Fear of Progression Questionnaire-Short Form (SF) or ≥ 24 on the Impact of Event Scale-Revised
  • All subjects must have the ability to understand and the willingness to sign a written informed consent

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
City of Hope Medical Center
Coordinator of this site? Confirm its status
DuarteUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.