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Childhood Cancer Survivors clinical trials

View clinical trials related to Childhood Cancer Survivors.

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NCT ID: NCT05641636 Completed - Clinical trials for Childhood Cancer Survivors

Cardiovascular Disorders and Risk Factors in Childhood Cranial and Craniospinal Tumors Survivors

Start date: November 11, 2019
Phase:
Study type: Observational

The purpose of research is to study to adverse cardiovascular disorder and risks factors in childhood cranial and craniospinal tumors survivors. In this research the investigators investigate cardiological instrumental diagnostic, such as electrocardiography, echocardiography with the determination of global longitudinal strain, cardiopulmonary exercise test, and diagnostic of endothelial function by Angioscan for the prediction of cardiovascular complications after cranial and craniospinal radiotherapy and chemotherapy.

NCT ID: NCT05562193 Recruiting - Clinical trials for Childhood Cancer Survivors

Exercise and Pain in CCS

Start date: September 30, 2022
Phase: N/A
Study type: Interventional

The purpose of this study is to demonstrate that integration of exercise intervention into standard post-cancer directed treatment care will improve patient reported pain, decrease the need for medications to manage chronic pain and improve functional and psychosocial outcomes in survivors of cancers in children and adolescents. Our central hypothesis is that integration of exercise interventions into standard post-cancer directed treatment care will be acceptable and feasible while improving patients' pain, decreasing the cumulative dose of pain medication and improving patients' functional and psychosocial outcomes as compared to patients who only receive standard post-cancer directed treatment care.

NCT ID: NCT05527392 Recruiting - Clinical trials for Childhood Cancer Survivors

Virtual Health Insurance Navigation Pilot Program for Childhood Survivors (HINTII)

HINTII
Start date: May 1, 2023
Phase: N/A
Study type: Interventional

The investigators are conducting a Type I hybrid effectiveness-implementation trial to assess the effectiveness of HINT-S (synchronous) compared to enhanced usual care (EUC) in promoting health insurance literacy, thus reducing worry, unmet health care needs, and financial consequences due to medical costs to improve care and long-term outcomes of childhood cancer survivors. The investigators will also compare HINT-S to HINT-A (asynchronous), a prerecorded, asynchronous version of the 5 HINT-S navigator sessions.

NCT ID: NCT05463796 Recruiting - Lung Cancer Clinical Trials

InAdvance: Surveillance, Prevention, and Interception in a Population at Risk for Cancer

Start date: April 25, 2023
Phase:
Study type: Observational [Patient Registry]

This research study is creating a way to collect and store specimens and information from participants who may be at an increased risk of developing cancer, or has been diagnosed with an early phase of a cancer or a family member who has a family member with a precursor condition for cancer. - The objective of this study is to identify exposures as well as clinical, molecular, and pathological changes that can be used to predict early development of cancer, malignant transformation, and risks of progression to symptomatic cancer that can ultimately be fatal. - The ultimate goal is to identify novel markers of early detection and risk stratification to drive potential therapeutic approaches to intercept progression to cancer.

NCT ID: NCT04947709 Completed - Clinical trials for Childhood Cancer Survivors

Physical Activity Post-Cancer for Adolescents and Young Adults

PAPAYA
Start date: June 21, 2022
Phase: N/A
Study type: Interventional

The Physical Activity Post-Cancer for Adolescents and Young Adults (PAPAYA) trial aims to carry out a pilot randomized controlled trial among 10-17 year-old adolescents and young adults, at least 1 year and up to 5 years post-cancer treatment. The trial will evaluate the effects of a 12 week physical activity intervention to improve patient reported outcomes and physical function, in comparison to a delayed-intervention control group.

NCT ID: NCT04520061 Completed - Clinical trials for Childhood Cancer Survivors

Developing a Health Insurance Navigation Program for Survivors of Childhood Cancer

HINT
Start date: August 25, 2020
Phase: N/A
Study type: Interventional

Dr. Park and her colleagues published findings in the Journal of Clinical Oncology demonstrating that CCSS survivors, compared to siblings, were significantly more likely to be uninsured and to have difficulties obtaining health insurance. Given the current insurance landscape and the additional insurance burden that childhood cancer survivors face, the present study seeks to develop and pilot a health insurance navigation program targeted at feasibility and acceptability with survivors, and improving health insurance literacy and ameliorating financial distress related to medical costs. The proposed health insurance navigation will involve 4 navigator-led health insurance navigation sessions. The study investigators propose that, compared to the control arm (who will receive a health insurance information guide, but will not receive the navigation intervention), participants in the intervention arm will have improved health insurance literacy and decreased financial distress related to medical costs.

NCT ID: NCT04075734 Completed - Clinical trials for Childhood Cancer Survivors

Feasibility of a Self-Management + Peer Mentoring Intervention for Adolescent and Young Adult Childhood Cancer Survivors

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

The goal of this project is to evaluate the feasibility of the "Managing Your Health" online self-management skills+peer mentoring intervention that focuses on overcoming survivor barriers to self-management of their survivorship care. We will conduct a pilot randomized controlled trial (RCT) of the intervention versus usual care with adolescent and young adult survivors of childhood cancer ages 18-25 years. Participants will complete survey measures at baseline, Time 2 (about 2 months after baseline), Time 3 (about 5 months after baseline), and Time 4 (about 12 months after baseline).

NCT ID: NCT03523377 Recruiting - Clinical trials for Childhood Cancer Survivors

Overnight Fasting After Completion of Therapy: The OnFACT Study

Start date: April 27, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to test whether regularly not eating for at least 14 hours overnight ("intermittent fasting") is feasible and can improve blood sugar.

NCT ID: NCT02355340 Recruiting - Clinical trials for Bone Mineral Density

Bone Mineral Density Status in Pediatric and Adolescent Survivors of Childhood Cancer With History of Bone Fracture

Start date: May 2015
Phase:
Study type: Observational

This research study is evaluating bone mineral density in childhood cancer survivors who have a history of bone fracture.

NCT ID: NCT01948232 Withdrawn - Clinical trials for Childhood Cancer Survivors

Pilot Study of Perindopril in Childhood Cancer Survivors

Start date: September 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the feasibility of conducting a medical intervention trial in childhood cancer survivors with early echocardiographic evidence of cardiac remodeling.