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Search / Trial NCT06662435

GYNecologic Cancer-Related COGnitive Impairment

Launched by NORTHWESTERN UNIVERSITY · Oct 25, 2024

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Cognitive Impairment Gynecologic Cancer Cancer Related Cognitive Impairment

ClinConnect Summary

This clinical trial is looking to help women who have been diagnosed with gynecologic cancers, such as ovarian or cervical cancer, and have finished their chemotherapy treatment. Some of these patients experience difficulties with thinking and memory, often referred to as cognitive impairment. The study is testing a special training program that patients can do at home, designed to improve their cognitive abilities and help them feel better.

To be eligible for this trial, participants need to be women aged 18 and older who have completed chemotherapy and have reported some issues with their thinking skills. They must also speak and write in English and have internet access to take part in assessments. However, women with certain pre-existing mental health conditions or those currently involved in other cognitive training programs won’t be able to participate. If you join the study, you can expect to receive support tailored to your needs as you work on improving your cognitive skills from the comfort of your home.

Gender

FEMALE

Eligibility criteria

  • Inclusion Criteria:
  • Female; ≥18 years of age
  • Presents to clinic with a confirmed diagnosis of a gynecologic cancer (e.g., ovarian, endometrial, cervical, or vulvar cancer) who have completed adjuvant chemotherapy with at least stable disease at time of screening.
  • Screen positive for subjective cognitive impairment by answering affirmatively to at least one of three screener questions
  • Fluent in spoken and written English
  • Have access to the internet to complete assessments
  • Exclusion Criteria:
  • Patients who have not received chemotherapy
  • Patients with pre-existing neuropsychiatric disorders that would impact cognitive function, such as dementia, Alzheimer's disease, and schizophrenia.
  • Patients with non-gynecologic causes of incurable metastatic cancers.
  • Patients undergoing active interventions in other cognitive trials or patients currently using cognitive training programs such as Brain HQ, Luminosity, Elevate, Peak, Fit Brains, or CogniFit.
  • Patients with self-report of learning disability or an unwillingness to participate in technology-based cognitive training programs.
  • Pregnant women or prisoners
  • Patients with impaired-decision making capacity

About Northwestern University

Northwestern University is a prestigious academic institution renowned for its commitment to advancing medical research and improving patient care through innovative clinical trials. With a robust infrastructure that supports interdisciplinary collaboration, Northwestern leverages its expertise in various fields, including medicine, engineering, and social sciences, to drive groundbreaking studies. The university is dedicated to adhering to the highest ethical standards and regulatory compliance, ensuring that all clinical trials are conducted with the utmost integrity and focus on participant safety. Through its Clinical Trials Office, Northwestern aims to translate scientific discoveries into effective therapies, ultimately enhancing health outcomes and contributing to the broader medical community.

Locations

Chicago, Illinois, United States

Patients applied

0 patients applied

Trial Officials

Emma Barber, MD, MS

Principal Investigator

Northwestern University

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported