Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
Physical Activity
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentIntervention Model Description: The study has an active treatment group and an active control groupMasking: Triple (Participant, Care Provider, Outcomes Assessor)Masking Description: Study participants, group leaders, and outcomes assessors will not know the study objectives or hypotheses.Primary Purpose: Basic Science

Participation Requirements

Age
Between 45 years and 75 years
Gender
Both males and females

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 ...

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.

Tracking Information

NCT #
NCT03299348
Collaborators
Johns Hopkins University
Investigators
Principal Investigator: Manfred K. Diehl, PhD Colorado State University