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Factorial Trial Testing Guided Thinking Tasks to Optimize a Physical Activity Intervention

Factorial Trial to Test Unique and Combined Effects of Guided Thinking Tasks to Optimize a Physical Activity Intervention Among Underactive Adults

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05235360
Enrollment
192
Registered
2022-02-11
Start date
2022-02-14
Completion date
2023-07-31
Last updated
2022-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Physical Inactivity

Brief summary

The objective of this study is to optimize a novel, audio-recorded physical activity intervention that is scalable. Using principles of the Multiphase Optimization Strategy (MOST) framework, a full factorial study will test the unique and combined effects of different intervention components to identify which combination of components is optimal for increasing physical activity and mechanisms by which the components are or are not effective. This information will inform decisions about an optimal intervention package that is effective, efficient, and minimizes participant burden.

Detailed description

Eligible participants who provide informed consent will be enrolled in a 6-week study. At the baseline session, participants will be randomized to listen to a brief audio-recording of different guided thinking tasks. The audio-recordings are based on combinations of four different intervention components that will be tested in a 2 (positive affect imagery vs. neutral) x 2 (episodic future thinking vs. recent thinking) x 2 (action planning: yes, no) x 2 (dose: high vs. low) factorial trial. Participants will also complete a 30-minute brisk walking session on a treadmill. Participants will return for weekly visits in which they again listen to their assigned audio-recording and complete a 30-minute brisk walking session.

Interventions

BEHAVIORALAction planning

Participants will listen to a guided thinking task directing them to think about the remainder of their week and when, where, and how they plan to attain their remaining activity for the week.

BEHAVIORALHigh dose

Participants will listen to the audio-recording with the guided thinking tasks 5 times/week.

BEHAVIORALRecent thinking

Participants will listen to a guided thinking task directing them to think about a regular habit or activity they completed in the past week and to imagine that activity in specific and vivid detail.

Participants will listen to a guided thinking task directing them to think about themselves at a future, positive event and to imagine the event in vivid and specific detail.

BEHAVIORALPositive affect imagery

Participants will listen to a guided thinking task directing them to think about positive feelings and associations about physical activity in specific, personal, and positive detail.

BEHAVIORALNeutral imagery

Participants will listen to a guided thinking task directing them to imagine physical sensations (i.e., movements, muscles used) of a routine, daily activity (non-physical activity).

BEHAVIORALLow dose

Participants will listen to the audio-recording with the guided thinking tasks 1 time/week.

Sponsors

National Cancer Institute (NCI)
CollaboratorNIH
University of Kansas Medical Center
CollaboratorOTHER
University of North Carolina, Charlotte
CollaboratorOTHER
Southern Methodist University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 64 Years
Healthy volunteers
Yes

Inclusion criteria

* Adults ages 18-64 * Not currently meeting physical activity guidelines (\<150 minutes/week of self-reported moderate-to-vigorous physical activity) * Capable of providing informed consent * Access to a smartphone with active data plan * Willing to attend all study visits and comply with the protocol * Conversant in English

Exclusion criteria

* BMI \> 40 * orthopedic problems that would limit physical activity * self-reported coronary artery disease, stroke, COPD, chronic bronchitis, emphysema, diabetes

Design outcomes

Primary

MeasureTime frameDescription
Change in Weekly Physical Activity Minutes Across 6 Weeks (accelerometer-assessed)Assessed weekly at Weeks 1-6Amount of weekly moderate-to-vigorous (MVPA) minutes (i.e., minutes of MPVA weighted by intensity) will be determined from accelerometers (ActiGraph wGT3X-BT) worn for one-week periods for six consecutive weeks.

Secondary

MeasureTime frameDescription
Change in Weekly Physical Activity Minutes Across 6 Weeks (self-reported)Assessed weekly at baseline and at Weeks 1-6Amount of weekly self-reported MVPA (i.e., minutes of MPVA weighted by intensity) will be determined using the 7-day Physical Activity Recall (PAR) interview.

Other

MeasureTime frameDescription
Delayed DiscountingAssessed weekly at baseline and at Weeks 1-6The rapid delay discounting task will be assessed after listening to the audio-recording in-person (post-intervention). Will be assessed as a putative mechanism.
Affective Response to ExerciseAssessed weekly at baseline and at Weeks 1-6The Feeling Scale measures affective responses to exercise on a -5 to +5 scale with higher scores indicated a more positive affective response. It will be assessed during- and post-exercise for the in-person brisk walking sessions. Will be assessed as a putative mechanism.
Physical Activity IntentionsAssessed weekly at baseline and at Weeks 1-6The physical activity intentions scale (Conner et al., 2017) measures intentions for physical activity on a 1 to 5 scale with higher scores indicating stronger intentions. It will be assessed after the in-person brisk walking session. Will be assessed as a putative mechanism.
Action PlanningAssessed weekly at baseline and at Weeks 1-6The action planning scale (Sniehotta et al., 2005) measures action planning for physical activity on a 1 to 4 scale with higher scores indicating higher levels of planning. It will be assessed after listening to the audio-recording in-person (post-intervention). Will be assessed as a putative mechanism.
Intrinsic Motivation for ExerciseAssessed weekly at baseline and at Weeks 1-6The intrinsic subscale of the Behavioral Regulations in Exercise Questionnaire measures intrinsic motivation using a 0 to 4 response scale with higher scores indicating greater intrinsic motivation. It will be assessed after listening to the audio-recording in-person (post-intervention). Will be assessed as a putative mechanism.

Countries

United States

Contacts

Primary ContactColin Lamb, BA
colinl@smu.edu2147681545

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026