Cancer Survivor

8

Review clinical trials related to Cancer Survivor. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Leading Healthy Eating and Activity Promotion Program

The goal of the LEAP project is to improve the health and well-being of cancer survivors and their co-survivors living in persistent poverty areas by providing healthy behavior change support. This will be done by engaging the community in adapting beneficial approaches for promoting healthy diet and regular physical activity into a program for cancer survivors and co-survivors that is appropriate for the persistent poverty context and social determinants of health.

Participants needed: 100
Trial details
Age: 18-89Biological sex: AllType: InterventionalSponsor: University of Alabama at BirminghamUpdated: May 19, 2026Locations: 1
Eligibility criteria

Between the ages of 18 and 89 [+3]

Serious difficulty hearing [+3]

Status: Recruiting

Better Options for Chronic Cancer Pain

This proposal is relevant to the 240,000 cancer survivors who continue to use opioids long after they have successfully completed treatment for cancer at the VHA, placing them at risk of opioid addiction and overdose, and other opioid-related problems. Yet, there are no programs at the VHA to help them find alternatives to opioids, nor evidence to inform the choice of interventions. This study will meet these needs by examining four interventions that are effective at reducing opioid use in patients with chronic musculoskeletal pain but have yet to be tested in cancer survivors on long term opioid therapy. The proposed work is relevant to the VHA Pain Office's mission to provide Veterans better pain management while limiting the risks of long-term opioid therapy and it aligns with VHA Research and Development's priority to examine clinical interventions for tapering opioids. Successful completion this project will keep VHA at the forefront of the battle against the opioid epidemic with a strategy that may be adapted to address the same needs in non-Veterans.

Participants needed: 294
Trial details
Phase: Phase 4Age: 18-99Biological sex: AllType: InterventionalSponsor: VA Office of Research and DevelopmentUpdated: May 11, 2026Locations: 2
Eligibility criteria

Veterans must have had a qualifying solid tumor (bladder, breast, colorectal, he... [+4]

Veterans with total daily opioid doses >= 300 Morphine Milligram Equivalents (MM... [+8]

Status: Recruiting

Nutrition and Exercise Interventions for Androgen Deprivation Therapy-Induced Obese Frailty in Elderly and Non-Elderly Survivors of Advanced Prostate Cancer

This trial studies how well nutrition and exercise interventions work in reducing androgen deprivation therapy-induced obese frailty in prostate cancer survivors. Individualized nutrition and exercise advice for prostate cancer patients on androgen deprivation therapy may help to reduce obese frailty and change the levels of myokines in blood.

Participants needed: 50
Trial details
Age: 18+Biological sex: MaleType: InterventionalSponsor: Roswell Park Cancer InstituteUpdated: May 7, 2026Locations: 1
Eligibility criteria

Biopsy-confirmed prostate adenocarcinoma of any stage/grade [+8]

Known clinically significant severe chronic obstructive pulmonary disease (COPD)... [+5]

Status: Recruiting

An Acupuncture Study for Cancer Survivors With Joint Pain

The purpose of this study is to see whether acupuncture is a practical (feasible) treatment for cancer survivors with joint pain.

Participants needed: 60
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Memorial Sloan Kettering Cancer CenterUpdated: Oct 10, 2025Locations: 2
Eligibility criteria

English- or Spanish-speaking adults [+7]

Completed active treatment (chemotherapy, surgery, radiation, transplantation) <... [+6]

Status: Recruiting

Making Healthy Habits Stick

The aim of this project is to help increase physical activity maintenance in cancer survivors.

Participants needed: 260
Trial details
Age: 19+Biological sex: FemaleType: InterventionalSponsor: University of TennesseeUpdated: Oct 1, 2025Locations: 2
Eligibility criteria

woman age of 19 or older [+18]

Metastatic or recurrent cancer [+24]

Status: Recruiting

Studying Health Outcomes After Treatment in Patients With Retinoblastoma

This trial studies health outcomes after treatment in patients with retinoblastoma. Gathering health information over time from patients and family members through vision assessments, samples of tissue and saliva, and questionnaires may help doctors learn more about what causes retinoblastoma, identify long-term health outcomes for patients with retinoblastoma, and find out which therapies may be the best for treating retinoblastoma

Participants needed: 900
Trial details
Biological sex: AllType: ObservationalSponsor: Vanderbilt-Ingram Cancer CenterUpdated: Sep 19, 2025Locations: 11
Eligibility criteria

Unilateral or bilateral intraocular retinoblastoma [+11]

Status: Recruiting

LOG-I - Impact Study of LOG-AFTER Software on Long-term Monitoring of Former Patients (LOG-I - LOG-Impact Study)

Childhood cancer survivors represent a high-risk population that requires risk-based follow-up. Follow-up recommendations have been harmonized. Education and information practices regarding follow-up recommendations should be personalized, to ensure understanding by all survivors, including those with neurocognitive disorders. Individualized follow-up is necessary to detect complications that may increase morbidity and decrease quality of life, or even increase the risk of early mortality. In France, the LOG-AFTER software was developed in 2017 by university hospital of Angers and Epiconcept (approved health data host). The main differences with the European procedure concern radiotherapy information, the link with the General practitioner (GP), and the possible addition of information and/or access to therapeutic education in a video format. Indeed, there is the possibility of creating an GP account allowing to receive notifications concerning the follow-up of his patient to be scheduled, to have access to his file summary and his personalized follow-up plan, various information and blank prescription models. LOG-I is a study of the impact of the LOG-AFTER software for the "patient/GP" couple on adherence to follow-up recommendations. LOG-I is interested in all former patients with at least 3 recommendations in their personalized follow-up plan, taking into account the specific population of patients cured of a brain tumor.

Participants needed: 320
Trial details
Age: 15+Biological sex: AllType: InterventionalSponsor: University Hospital, AngersUpdated: Jul 2, 2025Locations: 1
Eligibility criteria

Previously treated for cancer or malignant hematological pathology before the ag... [+5]

Patient who has relapsed or developed a second cancer with a post-treatment dela... [+2]

Status: Recruiting

Health and Exercise Response in Children With Chronic and Auto-immune Pathologies

The aim of the present project is to assess the effects of the chronic diseases and their associated treatments chronic paediatric diseases (CPD), to further understand their impact on physical fitness for public health perspectives. This is an innovative approach in the treatment of chronic paediatric diseases . This project should yield results that help improving treatments for children and adolescents with chronic paediatric diseases throughout physical activity as therapy, reduced pain, fatigue and inflammation, and improvement in physical fitness and life quality. The originality and novelty of this project is to combine architectural, functional and metabolic components of skeletal muscle to further understand the impact of chronic paediatric diseases as a function of treatment, disease activity and maturation status (prepubertal, pubertal or post pubertal). This study will aim at assessing muscular function (force production capacity and fatigability) in specific or ecologic situations so as to get information about muscle functioning on isolated muscle group (here knee extensors) or during whole body exercise. Moreover, results arising from muscle architecture or quality will allow understanding the decrease in strength or endurance reported in the literature. The data collected will allow us to further understand the impact of the disease on structural, functional and metabolic parameters. Finally, the understanding of these alterations will provide information enabling to establish recommendations in physical activity (PA) to reduce or even counter the effect of the chronic inflammation and prevent at long-term overweight and cardiovascular risks. The long-term objective is to contribute establishing recommendations or guidelines for prescribing physical activity during medical therapy. Values obtained in pathological children will be compared to those of control children matched for gender and maturation.

Participants needed: 300
Trial details
Age: 6-18Biological sex: AllType: InterventionalSponsor: University Hospital, Clermont-FerrandUpdated: May 8, 2019Locations: 1
Eligibility criteria

Aged between 6 and 18-year-old [+8]

Treatment by systemic corticoids (>1 week in the 30 days before test) [+5]