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Gynecologic Cancer clinical trials

View clinical trials related to Gynecologic Cancer.

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NCT ID: NCT04351139 Completed - Gynecologic Cancer Clinical Trials

Impact of the COVID-19 Pandemic in Gynecological Oncology

COVID-GYN
Start date: May 6, 2020
Phase:
Study type: Observational

The current infection with the Coronavirus SARS-CoV-2 (COVID-19) is an exceptional health situation which requires an adaptation of our management practices in gynecological oncology. Data from the literature suggest that infection with Coronavirus is serious in subjects with cancer with a risk of severe form 5 times higher than that of the population without cancer and a risk of death multiplied by 8. In addition, the risk of infection would be 3 times greater in case of cancer. Faced with the COVID-19 epidemic, the investigator must organize themselves to ensure continuity in the treatment of patients with gynecological cancer but also adapt our practices in the management (CPR, teleconsultation, adaptation of treatment or even postponement of treatment). The objective of the High Council of Public Health is to be able to ensure adequate oncological care avoiding any potential loss of chance concerning the care of cancer: people affected must, despite the pandemic, have care allowing the same level of curability (localized cancers) or the same life expectancy (advanced cancers). This must be done by limiting as much as possible the impact on the organization of the service, the organization of patient follow-up and the psychological impact that these possible modifications could have. The hypotheses of our study are that the exceptional health situation linked to this pandemic leads to a change in the care of patients with gynecological cancer associated with a psychological impact and increased anxiety of patients during their care. Despite the extent of the pandemic, very little existing data makes it possible to define recommendations with a sufficient level of evidence.

NCT ID: NCT04336683 Completed - Gynecologic Cancer Clinical Trials

Feasibility Study for Ultrasound-Guided Interstitial Brachytherapy for Gynecological CancersV2

Start date: February 17, 2015
Phase: N/A
Study type: Interventional

Brachytherapy treatment in gynecological cancers is an essential component to delivering adequate doses of radiation to a tumour while sparing normal tissue. Interstitial and intracavitary brachytherapy is often needed in advanced or recurrent disease, in cases where intrauterine brachytherapy may not deliver the optimal outcome. Interstitial brachytherapy is based on a defined template-and-needle system, and the procedure relies on clinical examination and pre-treatment imaging to guide needle insertion. There is currently no standard image-guided process to help direct needles in the pelvis. The investigators propose a 3D ultrasound device that will provide real-time imaging for the brachytherapy procedure which will aid in avoiding needle insertion into pelvic organs and result in optimal dose coverage to the tumour.

NCT ID: NCT04321135 Completed - Breast Cancer Clinical Trials

Avanzando Juntas: Adapting an Evidence Based Weight Loss Program for Hispanic Breast Cancer Survivors

Start date: November 1, 2019
Phase: N/A
Study type: Interventional

This study examine the feasibility and efficacy of Avanzando Juntas, a four-month community-based lifestyle intervention rooted in the evidence-based Moving Forward lifestyle intervention developed with and for AA breast cancer survivors. This intervention was adapted in collaboration with Hispanic/Latina BC & GC survivors. It will offer twice-weekly sessions aimed at supporting adherence to ACS nutrition and physical activity guidelines to promote weight loss and improved quality of life.

NCT ID: NCT04314284 Completed - Colorectal Cancer Clinical Trials

Patient-Centered Intervention to Reduce Cancer Patients' Financial Toxicity

Start date: May 26, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to incorporate feedback from cancer patients and providers to adapt, implement, and test an intervention. The intervention aims to prompt screening for financial distress, facilitate discussions about care costs with cancer patients, support health insurance selection, and ultimately reduce cancer patients' financial toxicity associated with cancer care.

NCT ID: NCT04298827 Completed - Quality of Life Clinical Trials

Gyn Onc Prehab Study

Start date: July 21, 2020
Phase: N/A
Study type: Interventional

Patients will be randomized to a unimodal or trimodal prehabilitation program prior to surgery for known or suspected gynecologic cancer.

NCT ID: NCT04281043 Completed - Quality of Life Clinical Trials

Quality of Life After Robotic Surgery for Endometrial Cancer

QoL
Start date: June 15, 2019
Phase:
Study type: Observational

The purpose of this study is to investigate how robotic assisted laparoscopic surgery affects the quality of life of women who are treated with primary surgery for endometrial cancer. So far, very little has been published and basically no long-term follow-up. Included patients respond to questionnaires preoperatively, 2 weeks after surgery and 3 months and 12 months after surgery. Each patient thus answers the questionnaires (the same) on four occasions. The questionnaires used are validated and used extensively internationally. The first survey has two parts, QLQ30 and the module for endometrial cancer EN24. In addition the study includes use PHQ -9 and GAD 7.

NCT ID: NCT04168242 Completed - Gynecologic Cancer Clinical Trials

Scalp Cooling in Gynecologic Cancer Patients

Start date: November 11, 2019
Phase: N/A
Study type: Interventional

In gynecologic cancers, many common chemotherapy agents can lead to chemotherapy-induced alopecia. Currently scalp cooling is the most well studied preventive measure. However, its acceptability and its impact on patients' QOL in Asian population is unclear.

NCT ID: NCT04068675 Completed - Ovarian Cancer Clinical Trials

Effects of Centering Pre-operative Counseling on Patient Reported Anxiety

Start date: February 24, 2020
Phase: N/A
Study type: Interventional

The primary objective of the study is to evaluate the effect of pre-operative counseling in a group setting on patient reported anxiety for patients scheduled to undergo surgery for a known or suspected gynecologic malignancy. Patient reported anxiety will be evaluated using a validated Patient-Reported Outcomes Measurement Information System (PROMIS) survey. We hypothesize that the group counseling session will reduce patient reported anxiety by a clinical meaningful level. Secondary objectives will evaluate the effect of the intervention on patient reported depression levels and compare adherence to Enhanced Recovery After Surgery (ERAS) instructions, utilization of unscheduled health care resources, and anxiety/depression levels to historical controls.

NCT ID: NCT03981731 Completed - Breast Cancer Clinical Trials

Management of Perioperative Anxiety by the Cardiac Coherence Technique Coupled With a Hypnosis Session

COHEC
Start date: February 14, 2020
Phase: N/A
Study type: Interventional

the investigator proposes to use the cardiac coherence technique coupled with a hypnosis session to improve post-operative recovery.

NCT ID: NCT03961217 Completed - Prostate Cancer Clinical Trials

Return to Work Among Cancer Survivors With Treatment-induced Survivorship Syndromes

Start date: January 1991
Phase:
Study type: Observational [Patient Registry]

The investigators plan to investigate the consequences of late effects (radiation-induced survivorship syndromes) after radiotherapy in Gynecological and Prostate cancer survivors on return to work (Yes/No) and if RTW happened then time to RTW. In addition, whether general health, type of work (occupation), work environment factors, individual factors (lifestyle, socioeconomic status etc.), contribute to the adverse late effects of radiotherapy and these Gynecological cancer survivors have a higher risk for disability pension/long term sickness absence (NOT Return to work).