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Breast Cancer clinical trials

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NCT ID: NCT04334096 Completed - Breast Cancer Clinical Trials

Long-term Improvement of Quality of Life in Breast Cancer Patients With Quality of Life Diagnosis and Therapy

Start date: May 30, 2016
Phase: N/A
Study type: Interventional

The purpose of the study is the long-term implementation of a system with quality of life diagnosis and tailored therapeutic options in order to improve quality of life of patients with breast cancer during follow-up.

NCT ID: NCT04330716 Completed - Breast Cancer Clinical Trials

Genetic Testing for Breast, Ovarian, Pancreatic, and Prostate Cancers

GeneBOPP
Start date: December 1, 2020
Phase: N/A
Study type: Interventional

This study is evaluating the effect of two pre-test education methods on participants interested in genetic testing for hereditary cancer risk.

NCT ID: NCT04330339 Completed - Breast Cancer Clinical Trials

Prolonged Nightly Fasting in Breast Cancer Survivors

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

This study is being done to examine whether fasting for 13 hours every night is feasible and if it can help breast cancer survivors lose weight and improve their health. - Previous studies have found that women who are overweight or obese when their breast cancer is found (diagnosed) have a greater risk of their breast cancer recurring. Recent research suggests that prolonged nighttime fasting (>13 hours) may improve the risk of recurrence for breast cancer. - This study will examine if fasting for 13 hours per night is doable for participants and will also study what the effect of fasting is on quality of life, mood, fatigue, body size, and markers of health in the blood.

NCT ID: NCT04330040 Completed - Breast Cancer Clinical Trials

Prospective Multicentre Phase-IV Clinical Trial of Olaparib in Indian Patients With Ovarian and Metastatic Breast Cancer

SOLI
Start date: May 30, 2020
Phase: Phase 4
Study type: Interventional

A Prospective, Multicentre, Phase-IV Clinical Trial of Olaparib in Indian Patients with Platinum Sensitive Relapsed Ovarian Cancer who are in Complete or Partial Response Following Platinum based Chemotherapy and Metastatic Breast Cancer with germline BRCA (BReast CAncer gene) 1/2 Mutation

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: NCT04317690 Completed - Breast Cancer Clinical Trials

Online Trial Examining Validity and Reliability of the Shared Decision Making Process Survey

Start date: March 17, 2020
Phase:
Study type: Observational

The purpose of this study is to survey a sample of adults who have recently made a decision about treatment of high cholesterol or high blood pressure or a decision about screening for colorectal cancer, breast cancer, or prostate cancer. The main goal is to gather evidence of the validity and reliability of the Shared Decision Making Process scale. Secondary goal is to gather evidence on the quality of decisions for these common medical situations.

NCT ID: NCT04316156 Completed - Breast Cancer Clinical Trials

Real-time Interactive Digital Healthcare System in Patients With Breast Cancer; Randomized Controlled Trial

Start date: April 1, 2020
Phase: N/A
Study type: Interventional

This study aims to examine the effect of hospital-home linkage short-term rehabilitation therapy using real-time interactive digital healthcare system (Uincare Homeplus) in post-operative patients with breast cancer. This is prospective study. 100 breast cancer patients who underwent axillary lymph node diessection or breast reconstruction following mastectomy will be examined, and those with limited range of motion (ROM) of affected shoulder will be enrolled in the study. Shoulder ROM, Quick-DASH, pain evaluation with NRS, quality of life evaluation with FACT-B and EQ-5D will be evaluated on enrollment, 4-week, 8-week, and 12-weeks after enrollment.

NCT ID: NCT04315012 Completed - Breast Cancer Clinical Trials

Training With Mobile Application in Breast Cancer

Start date: January 10, 2018
Phase: N/A
Study type: Interventional

Endocrine hormonal therapy (EHT) applied to avoid recurrence and metastasis of the breast cancer has also side effects which do not threaten life; however, it does negatively effects quality of life. The objective of this study was to determine the effects on quality of life of a mobile app-based (e-mobile) education for supportive care of patients with breast cancer receiving adjuvant endocrine hormonal therapy. The data were collected to with face to face and/or telephone interviews at 2 time points: prior to the initiation (T0) and after the completion (T1) of mobile app-based education. Patients were received education via mobile app for 12 weeks during which they were contacted in every 15 days; a mobile app-based (e-mobile) education was provided, including information about breast cancer definition, treatment process, symptoms management, adequate nutrition, regular physical activity and coping with stress. In this process, the control group patients were provided with standard care.

NCT ID: NCT04309929 Completed - Breast Cancer Clinical Trials

Description of the Analgesia Obtained With the Anesthesiological Protocols Currently Used in Breast Surgery

Start date: September 12, 2016
Phase:
Study type: Observational

This study aims to describe the pain-relieving effect obtained with the current post-surgery pain control methods used in breast surgery by measuring the painful sensation and the consumption of opioids in the first 24 post-surgery hours. It also aims to describe the appearance of any complications such as post-surgery nausea and vomiting. Current anesthesia involves the combined use of intravenous painkillers and anti-inflammatory drugs such as acetaminophen, ketorolac, tramadol or morphine (the latter via PCA system = patient-controlled analgesia) or for local administration at the surgical site level ( local anesthetics). It is also proposed to describe the intensity and interference of pain in daily activities

NCT ID: NCT04307407 Completed - Breast Cancer Clinical Trials

Exercise in Breast Cancer Survivors

Start date: September 8, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the effects of aerobic exercise to usual care in women treated with chemotherapy and radiation therapy for non-metastatic breast cancer