Physical Activity Clinical Trial
Official title:
A Couple-Based Physical Activity Intervention for Cancer Survivors
This pilot study will develop and test a couple-based physical activity intervention among
cancer survivors and their partners.
Aim 1: To determine the feasibility and acceptability of a couple-based physical activity
intervention for cancer survivors. Feasibility will be quantified using rates of study
eligibility, overall accrual, attrition, and adherence to the study protocol. Acceptability
will be assessed via couples' ratings on a standardized measure of treatment effectiveness/
satisfaction, supplemented open-ended questions
Aim 2: To provide preliminary data on the effects of a couple-based physical activity
intervention relative to a wait list control group on survivor outcomes (i.e., level of
physical activity, quality of life, self-efficacy for achieving and maintaining physical
activity goals, perceived partner support for physical activity, and quality of the
survivor-partner relationship). The investigators hypothesize that the intervention will
produce benefits in each of these domains.
Aim 3: To provide preliminary data on the effects of a couple-based physical activity
intervention relative to a wait list control group on partner outcomes (i.e., partner's level
of physical activity, self-efficacy for helping the survivor achieve and maintain physical
activity goals, and quality of the survivor-partner relationship). The investigators
hypothesize that the couple-based intervention will produce benefits in each of these
domains.
Background and Significance:
Physical activity (PA) is an essential part of cancer survivors' treatment plan as it helps
prevent recurrence and improves cardiovascular fitness and downstream cardiovascular risk,
the cause for most deaths in cancer survivors. Additional benefits of increasing PA include
improvements in body composition, physical function, psychological outcomes, and quality of
life. However, most survivors are not sufficiently active and would benefit from an
intervention to promote PA. Prior PA interventions for cancer survivors have had mixed
success. A recent systematic review identified 14 RCTs testing exercise interventions among
sedentary cancer survivors and concluded that there was insufficient evidence that existing
interventions are successful in achieving recommended levels of PA. In particular, there has
been a lack of attention to psychosocial aspects of changing behavior, and to strategies that
promote independent exercise behavior that can be maintained over time. Thus, it is clear
that novel approaches to PA interventions are needed.
Design:
This is a two-arm randomized controlled trial to evaluate a couple-based physical activity
(PA) intervention that systematically trains partners in skills to support the survivor in PA
initiation and maintenance strategies.
Couples randomized to Arm 1 (the Couples-Based Physical Activity Intervention) will receive
four 60-minute intervention sessions via videoconference with Duke staff. Study staff will
provide couples with instructions for use of the iPad computer (if provided by the study) and
videoconference software which will be used to deliver the intervention sessions. Couples
will also be provided with contact information for technical support. The first 3 sessions
will be conducted weekly, with a booster session occurring approximately one month later. The
intervention will include components to (a) encourage couples' favorable outcome expectations
about the benefits of working together to initiate and maintain increases in PA, (b) build
their confidence that they can work together to accomplish their goals, and (c) help them
identify and use communal strategies, such as couple communication and joint decision making
about goals and plans for increasing physical activity, and working through barriers to
making these changes. Finally, the intervention will incorporate important behavior change
techniques that have been found to help people change their exercise behavior, such as goal
setting, self-monitoring of behavior, and prompts for practice, adapting them to a communal
coping approach. Treatment sessions will be audio recorded for QA purposes.
Those randomized to Arm 2 (waitlist control) will have the option to receive the intervention
after they complete the follow-up survey. This version of the intervention will not include
the booster session, so will last approximately 1 month in total. If they choose to receive
the intervention, they will be provided with a tablet computer if they do not have one.
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