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临床试验/NCT05649371
NCT05649371尚未招募不适用

A Multiphasic Prehabilitation Exercise Program For Allogeneic Hematopoietic Stem Cell Transplant Recipients

University of Calgary0 个研究点目标入组 60 人开始时间: 2023年1月最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
60
主要终点
Feasibility of Implementing an Exercise Program for Patients Undergoing Allogeneic-HSCT, Measured by Participant Attendance

研究概览

简要总结

The purpose of this study is to implement a prehabilitation intervention to enhance recovery for people undergoing allogeneic stem cell transplant for hematologic malignancies. All participants in this study will receive a prehabilation intervention in addition to usual care (no change to their chemotherapy protocols or transplant) and several quality of life and fitness scores will be measured throughout the intervention.

研究设计

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

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adult patients, 18 years or older, undergoing an allo-HSCT for acute leukemia.
  • Approval to engage in exercise as per screening by the CSEP or ACSM certified CEP and/or clinician
  • Ability to provide written informed consent and understand study information.

排除标准

  • Less than 18 years old
  • Diagnosed with acute leukemia but not undergoing work-up for allo-HSCT
  • Unable to read/communicate in English (i.e., unable to complete experimental procedures such as patient-reported outcomes).
  • Neurological or musculoskeletal comorbidity inhibiting exercise.
  • Diagnosed psychotic, addictive, or major cognitive disorders.
  • Severe coronary artery disease (Canadian Cardiovascular Society class III or greater).
  • Significant congestive heart failure (New York Heart Association class III or greater).
  • Severe thrombocytopenia (platelets <10) - ok if transfused platelets prior to exercise.

结局指标

主要结局

Feasibility of Implementing an Exercise Program for Patients Undergoing Allogeneic-HSCT, Measured by Participant Attendance

时间窗: 6-9 months

Review participant attendance/participation in the program and the questionnaires.

次要结局

  • Amount of Physical Activity Measured With Activity Tracker(6-9 months)
  • Exercise Behaviour Measured with Modified Godin Leisure Time Exercise Questionnaire(6-9 months)
  • Patient Quality of Life Measured with the Functional Assessment of Cancer Therapy-Bone Marrow Transplant and EuroQol 5 Dimension 5 Level Questionnaire(6-9 months)
  • Level of Fatigue Measured with the Functional Assessment of Chronic Illness Therapy Fatigue Scale (FACIT-F) Questionnaire(6-9 months)
  • Amount of Anxiety and depression Measured with the Hospital Anxiety and Depression Scale (HADS) Questionnaire(6-9 months)
  • Amount of Symptom burden Measured with the Edmonton Symptom Assessment System-revised (ESAS-r) Questionnaire(6-9 months)
  • Patient's Performance Status Measured by the Eastern Cooperative Oncology Group (ECOG) Scale(6-9 months)
  • Handgrip Strength Measured by Handgrip Dynamometry(6-9 months)
  • Balance Measured by Single Leg Stance Test(6-9 months)
  • Lower Limb Muscular Endurance Measured with 30-second sit-to-stand Test(6-9 months)

研究者

申办方类型
Other
责任方
Sponsor

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