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临床试验/NCT02770781
NCT02770781已完成不适用

Feasibility Study of the Addition of a Personal Trainer to the Post-Treatment Regimen of Breast Cancer Survivors

University of Pittsburgh2 个研究点 分布在 1 个国家目标入组 68 人开始时间: 2015年10月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
68
试验地点
2
主要终点
Study recruitment ability

研究概览

简要总结

The purpose is to examine the feasibility and preliminary effectiveness of the role of a personal trainer for non-metastatic breast cancer survivors to improve physical activity and well-being (in terms of quality of life).

详细描述

After breast cancer treatment, many women are faced with effects of treatment such as changes in appearance, fatigue, and reduced quality of life as compared to the pre-disease state. An intervention to increase physical activity may be helpful to improve well-being and outcomes for women treated for breast cancer.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Post active breast cancer therapy (e.g. surgery and/or chemotherapy and/or radiation therapy), but may still be undergoing maintenance cancer therapy.
  • Free of macro-metastatic disease
  • Sedentary pre-cancer diagnosis: Those individuals not participating in a regular exercise program or not meeting the minimal physical activity recommendations from the General Surgeon which is accumulating 30 minutes or more of moderate physical activity on most days of the week
  • Ability to provide informed consent
  • Ability to provide a written physician's clearance
  • Patients must be new to the Survivorship Clinic (within first 12 months).

排除标准

  • Medical conditions that would preclude participation in a weight-training program.
  • Those who plan on relocating outside the Greater Pittsburgh Area in the next 3 months of intervention.

研究组 & 干预措施

Personal Trainer

Experimental

All subjects will meet a set amount of times with a personal trainer over the course of the study to participate in an exercise regimen.

干预措施: Exercise regimen (Other)

结局指标

主要结局

Study recruitment ability

时间窗: Baseline through ~ 6 months of follow-up.

Pilot study

次要结局

  • Physical fitness(Baseline through ~ 6 months of follow-up.)
  • Change in physical activity self-efficacy questionnaire(Baseline and ~ 6 months)
  • Functional Assessment of Cancer Therapy - Endocrine Symptoms(Baseline and ~ 6 months)
  • Change in Paffenberger Exercise habits questionnaire(Baseline and ~ 6 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Van Londen, Gijsberta

Assistant Professor

University of Pittsburgh

研究点 (2)

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