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AgingPLUS: Promoting Physical Activity in Adults

Testing Psychological Mechanisms to Promote Physical Activity in Adults

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03299348
Enrollment
402
Registered
2017-10-03
Start date
2018-05-01
Completion date
2023-05-31
Last updated
2025-06-19

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

Conditions

Physical Activity

Keywords

Psychological Mechanisms, Social-Cognitive Mechanisms

Brief summary

This study examines the efficacy of a psycho-educational intervention program, AgingPLUS, with regard to increasing middle-aged and older adults' engagement in physical activity.

Detailed description

AgingPLUS is a multi-component intervention program that addresses negative views of aging (NVOA), low internal control beliefs, and deficient goal planning as a risk cluster that keeps adults from engaging in health-promoting behavior. The program focuses on engagement in physical activity (PA) as the health behavior of choice. Engagement in PA is widely recognized as the best non-pharmacological, non-invasive, and cost-effective method of health promotion. Yet, only 20% of the adult population meets the recommended PA guidelines. This suggests that messages about the benefits of PA alone are not effective. Rather, it is essential to address the social-cognitive and motiva-tional mechanisms that prevent adults from adopting and maintaining a regular PA regimen. NVOA, low internal control beliefs, and deficient goal planning represent such a cluster of social-cognitive and motivational mechanisms. Given this background, the specific aims and hypotheses of the proposed research are: Aim 1: To conduct a randomized controlled trial examining the efficacy of the AgingPLUS program. Aim 2: To test a conceptual model of the mechanisms underlying the intervention effects. Aim 3: To conduct a 6-month follow-up to examine the longer-term effects of AgingPLUS. Upon completion of this project, we expect to have successfully established evidence for the efficacy of the AgingPLUS program (Stage II of the NIH Stage Mode). The long-term goal is to develop AgingPLUS into a full-fledged evidence-based program that can be implemented in community settings (e.g., senior centers), and can serve as a fairly brief and cost-effective public health tool to promote healthy and successful aging.

Interventions

BEHAVIORALAgingPLUS

The program consists of 2-hour meetings for a total of 4 weeks (total of 8 hours) and discusses (a) how negative views on aging and negative age stereotypes undermine adults' health-promoting behaviors; (b) how adults can take control of their own aging; and (c) how personal goals can be achieved through more effective goal planning and action plans.

BEHAVIORALActive Control Group

The program consists of 2-hour meetings for a total of 4 weeks (total of 8 hours) and discusses (a) four major health conditions that affect the lives of many middle-aged and older adults (e.g., cardiovascular disease, cancer, type 2 diabetes; clinical depression); and (b) how these conditions can be managed successfully.

Sponsors

Johns Hopkins University
CollaboratorOTHER
National Institute on Aging (NIA)
CollaboratorNIH
Colorado State University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
TRIPLE (Subject, Caregiver, Outcomes Assessor)

Masking description

Study participants, group leaders, and outcomes assessors will not know the study objectives or hypotheses.

Intervention model description

The study has an active treatment group and an active control group

Eligibility

Sex/Gender
ALL
Age
45 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

* Adults who engage in less than 60 minutes of PA per week and who intend starting a physical exercise program. * English speaking. * Willingness to be randomized to one of two programs. * Willingness to take part in the physical fitness tests and wear an accelerometer. * Willingness to commit to follow-up testing (i.e., not moving out of the area during the study period). * Physician clearance to take part in a submaximal exercise test and to begin an exercise program.

Exclusion criteria

* Signs of cognitive decline (defined as more than 4 errors on the Short Portable Mental Status Questionnaire). * Severe vision and/or hearing loss (obtained by self-report). * Serious problems with mobility. * A history of neurological, mental, or substance abuse disorders.

Design outcomes

Primary

MeasureTime frameDescription
Increased physical activityThis effect should be observable (1) at the Week-4 post-test, (2) the Week-8 post-test, and (3) the 6-Month post-test.We expect that participants significantly increase their engagement in physical activity as assessed by an accelerometer.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026