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Survivorship clinical trials

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NCT ID: NCT04552587 Completed - Clinical trials for Head and Neck Cancer

The HEART Study (Healthy Eating and Recovery Together)

Start date: December 4, 2020
Phase: N/A
Study type: Interventional

Head and neck cancer survivors and their primary caregivers (N=25 dyads) will be enrolled to pilot test a nutrition support system with a care planning clinic visit and a caregiver mobile App. Participants will be asked to complete baseline and 6-week follow-up surveys. The clinic session (offered in person or remotely) will include a needs assessment and a tailored care plan with information, educational materials and referrals about participants' symptoms, behaviors, social concerns and caregiving tasks. After the visit, the program will provide an App for caregivers with follow-up resources and mobile support for one month.

NCT ID: NCT04431921 Completed - Survivorship Clinical Trials

Assessment of Functional Capacity, Pain, Cognitive and Respiratory Functions in Lung Cancer Survivors

Start date: July 17, 2017
Phase:
Study type: Observational

Serious side effects occurs with disease and treatments in survival after lung cancer. For this reason, functional capacity, cognitive status, pain perception and respiratory functions may be affected in lung cancer. The purpose of this study was to evaluate respiratory function, respiratory muscle strength and endurance, functional capacity, pain, cognitive status level, and physical activity in lung cancer patients and compare with the findings of healthy subjects

NCT ID: NCT04430335 Completed - Cancer Clinical Trials

Telephone-Based Intervention to Treat Depression and Anxiety in Hispanic Cancer Survivors

Start date: January 4, 2021
Phase: N/A
Study type: Interventional

The purpose of this research is to assess the feasibility of administering a telephone-based intervention to treat depression and anxiety in Hispanic cancer survivors.

NCT ID: NCT04337203 Completed - Cancer Clinical Trials

Shared Healthcare Actions and Reflections Electronic Systems in Survivorship

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

The primary purpose of this study is conduct a pilot study testing the study protocols, implementation program, and mixed-methods data collection.

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: NCT04227353 Completed - Colorectal Cancer Clinical Trials

Healthy Eating and Active Lifestyle After Bowel Cancer: HEAL ABC

HEALABC
Start date: January 30, 2021
Phase: N/A
Study type: Interventional

Trial Design: This is a feasibility randomised controlled trial. Aim: The study aims to test the Healthy Eating and Active Lifestyle After Bowel Cancer - HEAL ABC intervention and HEAL ABC resources for feasibility and will inform a future definitive randomised controlled trial (RCT). Objectives: 1. Is it practical to run HEAL ABC study as a definitive randomised controlled trial? 2. Adherence to intervention, motivations, barriers and facilitators of CRC survivors to follow HEAL ABC. Study Population: Colorectal cancer survivors who completed surgery and/or active treatment. Intervention: The intervention group will use HEAL ABC resource with supportive telephone calls every two weeks during the intervention period and once a month during the follow up period. Control: Participants follow standard care recommendations. Timing and duration: 3 months intervention with 6 months follow up period

NCT ID: NCT04163042 Completed - Cancer Clinical Trials

Physical Activity Counselling for Young Adult Cancer Survivors

Start date: March 1, 2021
Phase: N/A
Study type: Interventional

Survival rates for cancer are increasing, resulting in more young adult cancer survivors living with lingering side effects. Physical activity has been shown to improve the quality and length of life in young adult cancer survivors; yet, few are active enough, and little is currently being done to promote physical activity in this population. The investigators developed a novel behaviour support intervention to promote physical activity in young adult cancer survivors. In this two-arm pilot randomized controlled trial, the investigators aim to: (1) assess trial and intervention feasibility, (2) assess trial and intervention acceptability, and (3) generate data on physical activity behaviour. Young adult cancer survivors will be randomized to receive either a 12-week behaviour support intervention delivered via videoconferencing or will be allocated to usual care.

NCT ID: NCT04066218 Completed - Sexual Dysfunction Clinical Trials

Sexual Function Screening in Childhood Cancer Survivors

Start date: September 16, 2019
Phase:
Study type: Observational

This is a qualitative research study involving semistructured interviews and Think-Aloud methodology during completion of a clinical screening tool. All participants will undergo the same semistructured interviews.

NCT ID: NCT03993561 Completed - Clinical trials for Head and Neck Cancer

Treatment Summary and Survivorship Care Plans (TSSP)

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

The aim of the study is to establish the highest level of evidence to evaluate treatment summary and survivorship care plans (TSSPs) by piloting the TSSPs on patients with HNC. Hypothesis: HNC patients who receive the intervention of the TSSP will have an increased rate of implementation of recommendations for their needs, greater adherence with follow-up schedules, improved quality of life and improved satisfaction with post-treatment care. Aim 1 (Validation of TSSP): To validate a treatment summary and survivorship care plan (TSSP) intervention specifically tailored to the needs of HNC patients based on the best available evidence. Approach: In the first phase of the project the investigators will pilot the London Heath Sciences Centre TSSP with head and neck cancer survivors and then have the TSSP extensively reviewed and modified by our multidisciplinary head and neck oncology treatment team. Aim 2 (Evaluation of TSSP): To evaluate the implementation of a TSSP in survivors of head and neck cancer compared to usual treatment in a randomized fashion to determine whether TSSPs result in improved implementation of recommendations for HNC survivors and improved quality of life and satisfaction. Approach: In the second phase of the project the investigators will conduct a randomized controlled trial to compare patient reported outcomes in HNC patients who have received the TSSP to patients who have not received the TSSP.

NCT ID: NCT03879096 Completed - Cancer Clinical Trials

Clinical and Functional Variables in Oncology

Oncolab
Start date: May 1, 2016
Phase: N/A
Study type: Interventional

The aim is to analyse the effect of a Therapeutic Exercise and Education programme in several clinical and functional outcomes in cancer patient and survivors