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临床试验/NCT07643389
NCT07643389已完成不适用

EXCEL-Punjabi: Tailored Exercise Oncology for the South Asian Population

University of Calgary1 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2025年7月1日最近更新:
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
12
试验地点
1
主要终点
Measurement Completion

研究概览

简要总结

The goal of this pilot feasibility study is to explore the feasibility and exploratory effects of a culturally-tailored exercise oncology intervention in Punjabi-speaking individuals of South Asian heritage and their support persons. The main questions it aims to answer are:

  1. What is the feasibility and acceptability of the EXCEL-Punjabi intervention?
  2. What are the exploratory effects (i.e., psychosocial and physical changes) before and after program delivery?

Participants will take part in a 12-week exercise oncology intervention consisting of twice weekly hour long multimodal circuit-based exercise sessions. They will also complete questionnaires and functional fitness assessments pre- and post- 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
Supportive Care
盲法
None

入排标准

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

入选标准

  • •Punjabi-speaking
  • •Self-identified as being of South Asian heritage
  • •over the age of 18
  • •pre-, post-, or currently receiving cancer treatment or a support person of an individual living with and beyond cancer
  • •cleared to participate in, at minimum, mild intensity exercise by a Clinical Exercise Physiologist
  • •Able to provide informed consent

排除标准

  • •under the age of 18
  • •not cleared to exercise by a Clinical Exercise Physiologist

研究组 & 干预措施

EXCEL-Punjabi

Experimental

Culturally Tailored Exercise Oncology Intervention

干预措施: EXCEL-Punjabi (Behavioral)

结局指标

主要结局

Measurement Completion

时间窗: Baseline to the end of the intervention (12 weeks)

Participants who completed all pre- and post- questionnaires and functional assessments

次要结局

  • Referrals(Baseline to end of intervention (12 weeks))
  • Consented(Recruitment to end of intervention (12 weeks))
  • Enrolled(Baseline (week 0))
  • Attendance(Baseline to end of intervention (12 weeks))
  • Adverse Events(Baseline to end of intervention (12 weeks))
  • Time Required to Deliver and Implement Intervention(From recruitment to end of intervention (12 weeks))
  • Physical Activity Level(Baseline to end of intervention (12 weeks))
  • Cancer related symptoms(Baseline to end of intervention (12 weeks))
  • Health Related Quality of Life(Baseline to end of intervention (12 weeks))
  • Fatigue(Baseline to end of intervention (12 weeks))
  • Cancer Related Quality of Life(Baseline to end of intervention (12 weeks))
  • Exercise Barriers Self-Efficacy(Baseline to end of intervention (12 weeks))
  • Cognition(Baseline to end of intervention (12 weeks))
  • Aerobic Capacity(Baseline to end of intervention (12 weeks))
  • Lower body strength(Baseline to end of intervention (12 weeks))
  • Upper extremity flexibility(Baseline to end of intervention (12 weeks))
  • Balance(Baseline to end of intervention (12 weeks))

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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