Green Exercise for Cancer - Creating Opportunities for Survivors

Status Recruiting

Clinical Trial Summary

The purpose of this study is to assess feasibility and acceptability for a trial to evaluate exercise behaviors, fatigue and exercise motivation in adolescent and young adult survivors of childhood cancer who participate in an outdoor exercise intervention compared to survivors who participate in an indoor exercise intervention. A pilot randomized cross over design will allow participants to be compared to traditional controls as well as self-controls.

Clinical Trial Description

Title: Green Exercise for Cancer - Creating Opportunities for Survivors (GECCOS) Rationale: Exercise is related to lower rates of late effects like fatigue, heart disease and second cancers among survivors of childhood cancer. Yet levels of exercise remain low among survivors. The context where exercise occurs - indoors or outdoors - may affect motivation to exercise and sustained exercise behavior. Yet the effects of exercise context on motivation and maintained behavior remain unexamined. This study aims to pilot test an outdoor exercise intervention for cancer survivors compared to attention controls receiving an indoor exercise intervention. Target Population: Adolescent (13 to 17 years) and young adult (18 to 30 years) survivors of any cancer or hematopoietic cell transplantation for non-malignant disease. Number of Participants : 16 to 20 participants (8 to 10 adolescents, 8 to 10 young adults). Objective: Pilot test, for feasibility and acceptability, a novel outdoor exercise intervention to motivate and maintain exercise in adolescent and young adult survivors of childhood cancer. Using a randomized cross-over design, participants will randomly receive both indoor and outdoor exercise sessions. Study Design: Randomized Cross-over Pilot Trial Measures of Interest: Primary Outcome - Accelerometer measured moderate to vigorous physical activity. Secondary Outcomes - Self-Determination Theory based measures of motivation to exercise from validated survey questions. Fatigue, measured with validated survey questions. Semi-structured qualitative exit interview will be used to assess acceptability and feasibility of the intervention. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03852758
Study type	Interventional
Source	University of Minnesota
Contact	Jonathan Miller, PhD
Phone	651-247-5096
Email	mill5687@umn.edu
Status	Recruiting
Phase	N/A
Start date	May 1, 2019
Completion date	December 1, 2024

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Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

Green Exercise for Cancer - Creating Opportunities for Survivors — GECCOS

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms