C.A.P.A.B.L.E. (CrossFit® and Physical Activity: A Better Life Experience)

Официальное название

Does High-Intensity Functional Training Improve Patient Movement and Quality of Life? A Study of CrossFit® in Cancer Survivors

Обзор

This study will introduce cancer survivors to cross-training with the expectation that the program proposed will ultimately result in superior improvements in functional performance, body composition and quality of life compared with the current American Cancer Society (ACS) guidelines for cancer survivors.

Подробное описание

A 12-week pilot intervention study introducing a high-intensity functional training program to 100 cancer survivors and evaluate the effects of this program on patient quality of life, functional capacity, and body composition. Response rates will be determined using various recruitment methods and estimate differences in response rates by patient characteristics including race, gender and age. Barriers to participation in the program in contacted patients who do not enroll as well as patients who enroll and do not complete the program will be described, as will participant satisfaction with enrolled participants who complete the program. The goal of this pilot study is to help refine the recruitment and program methods for a larger intervention study to test the superiority of a high-intensity interval functional training program compared with current American Cancer Society guidelines in improving functional capacity, body composition and patient reported quality of life.

Surveys will be completed by each participant weekly and physical assessments will be completed monthly.

Вмешательства

• Поведенческое 12 week pilot intervention study.
  Participants will begin a 12-week high-intensity functional training program conducted at CrossFit® in the D, located in downtown Detroit, Northville Athletix in Northville and Five Lakes CrossFit® in Farmington Hills.

Первичные конечные точки

• Enrollment rates [Срок оценки: Baseline]
• Change in functional performance and variability in functional performance among adult cancer survivors enrolled in a high-intensity functional training program [Срок оценки: Baseline to 12 weeks]
• Change in functional performance and variability in functional performance among adult cancer survivors enrolled in a high-intensity functional training program [Срок оценки: Baseline to 12 weeks]
• Change in functional performance and variability in functional performance among adult cancer survivors enrolled in a high-intensity functional training program [Срок оценки: Baseline to 12 weeks]
• Change in self-reported health-related quality of life (HRQOL) and variability using the FACT questionnaire [Срок оценки: Baseline to 12 weeks]
• Change in Body Composition [Срок оценки: Baseline to 12 weeks]
• Change in Body Composition [Срок оценки: Baseline to 12 weeks]
• Change in Body Composition [Срок оценки: Baseline to 12 weeks]
• Change in Body Composition [Срок оценки: Baseline to 12 weeks]
• Change in Body Composition [Срок оценки: Baseline to 12 weeks]

Критерии участия

Критерии включения

• Aged 18 years or older at time of program recruitment
• Diagnosed with any cancer
• Cleared from their physician to participate in the program (We assume that most patients will have completed treatment, however if a patient is currently under treatment, this should be their oncologist. If the patient is not currently undergoing treatment, this could be primary care physician or oncologist).
• Available transportation to and from the facility on session days

Критерии исключения

• Widely metastatic cancers to the brain or bone may be excluded.
• Patients using mobility assistance devices may be excluded. Exclusionary criteria will be reviewed on a case-by-case basis and patients with these limitations may be included with approval from Dr. Beebe-Dimmer and the referring physician.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение

Не применимо

Модель

Одна группа

Маскирование

Открытое

Основная цель

Лечение

Центры проведения

США · 1 центр

• Barbara Ann Karmanos Cancer Institute — Detroit

Идентификаторы

NCT: NCT03750981 · 2018-091

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

Открыть это исследование на ClinicalTrials.gov ↗