iMETX (Individualized Metabolic RX): a Pilot Study
Ключови думи
Резюме
Описание
Objectives The investigators hypothesize that developing an individualized and dynamic exercise intervention (iMETX) that accounts for factors of the built environment will be feasible for breast cancer patients following primary treatment. This pilot study will assess the feasibility and provide preliminary estimates of effectiveness of the environmental intervention for increasing the energy expenditure and energetic capacity of breast cancer patients. The investigators will also explore patient feedback with this intervention and changes in levels of fatigue and quality of life. Experience and data from this initial pilot study will be used to refine the intervention and design subsequent studies to test its effectiveness.
Primary objective Evaluate the feasibility of an individualized, dynamic, environmental physical activity intervention for early stage breast cancer patients following primary treatment.
Secondary objectives
1. Determine a preliminary estimate of effect size of the environmental intervention on energetic capacity (power envelope) as measured by Power Protocol-B
2. Determine a preliminary estimate of effect size of the environmental intervention on average daily EE as measured by a wearable hybrid GPS/accelerometer physical activity monitor
3. Determine the effect of the environment intervention on the physical parameters of BMI and lean body mass
4. Determine the effect of the environmental intervention on patient reported fatigue and quality of life
5. Determine the persistence of changes in average daily EE after the intervention is complete (i.e., when individual movement tasks are no longer suggested).
6. Obtain formal and informal patient feedback throughout and after the intervention to assess satisfaction and perceptions of feasibility
7. Assess safety
Exploratory objectives Blood samples will be collected prior to and following the intervention and banked for future correlative studies, including the following: inflammatory cytokines (high sensitivity C reactive protein and interleukin 6), adipokines (adiponectin and leptin), sex hormones (estradiol, estrone, testosterone, and sex hormone binding globulin), and telomere length. In addition the invstigators will explore correlations of built and social environment characteristics and psychosocial characteristics with pre-intervention and changes in energy expenditure.
Дати
| Последна проверка: | 01/31/2020 |
| Първо изпратено: | 05/15/2017 |
| Очаквано записване подадено: | 05/15/2017 |
| Първо публикувано: | 05/17/2017 |
| Изпратена последна актуализация: | 02/13/2020 |
| Последна актуализация публикувана: | 02/16/2020 |
| Действителна начална дата на проучването: | 05/14/2017 |
| Приблизителна дата на първично завършване: | 03/31/2019 |
| Очаквана дата на завършване на проучването: | 03/31/2019 |
Състояние или заболяване
Интервенция / лечение
Behavioral: iMETX intervention
Фаза
Групи за ръце
| Arm | Интервенция / лечение |
|---|---|
| Experimental: iMETX intervention Individualized exercise recommendation | Behavioral: iMETX intervention Pre-intervention the participants will wear the running watch for 3 weeks so that researchers can collect data about their daily routines regarding where and how much energy they expend.
During the intervention participants will wear the running watch for 12 weeks. Every 1-3 days the participants will be given an individualized recommendation for how to increase their activity via the iMETX application. Participants will be able to provide feedback to the researchers throughout intervention period regarding what works and does not in terms of the recommendations for increasing activity.
Post-intervention the participants will wear the running watch for 12 weeks so that researchers can collect data in order to determine whether physical activity changes made during the intervention are sustained. |
Критерии за допустимост
| Възрасти, отговарящи на условията за проучване | 18 Years Да се 18 Years |
| Полове, допустими за проучване | All |
| Приема здрави доброволци | Да |
| Критерии | Inclusion criteria 1. Age ≥ 18 years 2. Diagnosis of DCIS or stage I, II, or III breast cancer 3. Completion of all primary therapy (with the exception of ongoing endocrine or trastuzumab therapy), including surgery, radiation, and/or chemotherapy greater than 4 weeks prior to study enrollment 4. Body weight less than 350 lbs., as dictated by the weight limit for DXA scanner 5. Regular access to a smart phone or computer Exclusion criteria 1. Any condition precluding exercise, including: NYHA class II, III, or IV congestive heart failure, uncontrolled angina, myocardial infarction in the prior 12 months, orthopedic surgery in the previous 6 months or plans for orthopedic surgery during the study period, chronic pulmonary conditions such as uncontrolled asthma (symptoms > 2 days/week) or dyspnea requiring oxygen, symptomatic peripheral vascular disease, symptomatic anemia, uncontrolled psychiatric conditions such as schizophrenia, or any other comorbidity that would interfere with the ability to complete and comply with the study protocol in the opinion of the investigator 2. Locally recurrent or metastatic breast cancer 3. Diagnosis of other active malignancy. Prior treated malignancies in addition to breast cancer are acceptable. 4. Pregnancy 5. Requirement of assistive devices (e.g., cane) for ambulation 6. Plans for moving to a new home or workplace during, pre-, or post-intervention period 7. Elective surgery anticipated during, pre-, or post-intervention period (e.g., breast reconstruction) 8. Inability to comply with the study procedures |
Резултат
Първични изходни мерки
1. Feasibility of intervention [24 months]
