Holistic Intervention for Cancer Survivors
Completed · Not applicable
Conditions studied: Cancer
In brief
There are many components to defining a cancer survivor's true quality of life. Quality of life (QOL) can be conceptualized as the maximum realization of an individual's potential outcomes of the physical, mental and spiritual aspects defining a human being. These levels of optimization are often limited within certain bounds by a survivor's medical history such as the cancer experience; functional capacities; dietary choices, connectedness and cognitive processing, e.g. perceptions about life situations such as stressors. Often, in intervention studies and within traditional Western medicine practice, focus on optimizing outcomes for cancer survivors is often "siloed", overly focusing on only one aspect of QOL and not accounting for improving other equally important aspects of QOL. A holistic approach, tailored to the unique aspects for that particular survivor, is needed to maximize the individuals overall QOL. Precision scientific data needs to be collected, as well as the cancer survivor's self-report perceptions (qualitative) to truly understand the individual's level of QOL. Thus, both quantitative and qualitative approaches are needed within a holistic approach. Many interventions' impact wanes when complete. Often those individuals that participated revert to previous maladaptive health behaviors. This can occur partly from a lack of a sense of ownership. Therefore, a holistic, structured approach is urgently needed, presented in a manner to enhance individual efficacy that enhances ownership. Strategies should also engage the expanded cancer survivor community thereby improving the health of the general cancer population, helping reduce existing cancer-related health disparities, and eliminating unnecessary costs on an already seriously strained public health system. Here the investigators propose a 16-week pilot project to prove the feasibility and initial efficacy of such a holistic approach to optimize outcomes for the physical, mental and spiritual aspects of QOL as measured with standard instrumentation and qualitative self-report for 30 adult cancer survivors in the San Antonio, Texas area. The investigators will conduct pre, post and a six-month follow-up assessment for QOL.
Key facts
- Study ID
- NCT06749938
- Run by
- The University of Texas Health Science Center at San Antonio
- People needed
- 29
- Starts
- 2020-01-15
- Expected to finish
- 2020-09-12
- Last updated by the study team
- 2024-12-27
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Have been given a diagnosis of any cancer in their lifetime; (active treatment or post treatment; but must be post diagnosis). (Even though the participant may be currently under treatment and limited in functionality, they will be included in the study as this pilot intervention is specifically intended to include any level of functionality, using a an individually designed program for optimizing outcome.)
- Have access or use of a mobile phone or computer to complete surveys and respond to text messages.
- Be able to speak understand English or Spanish.
- Oriented to time and place.
You may not qualify if…
- Currently enrolled in a competing protocol.
- Participants will be excluded it they present with any absolute contraindication to exercise testing as detailed by the American College of Sports Medicine Guidelines on Exercise Testing and Exercise Prescription 52. Specifically:
- Known significant change in the resting ECG suggesting significant ischemia.
- Recent myocardial infarction (within 2 days).
- Unstable angina.
- Uncontrolled cardiac arrhythmias causing symptoms or hemodynamic compromise.
- Severe symptomatic aortic stenosis.
- Uncontrolled symptomatic heart failure.
- Acute pulmonary embolus or pulmonary infarction.
- Acute myocarditis or pericarditis .
- Suspected or known dissecting aneurysm.
Where it is running
- Institute for Health Promotion Research — San Antonio, Texas, United States
Full record on ClinicalTrials.gov
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