Recruiting

MindWalk Intervention

Sponsor:

University of Illinois at Chicago

Code:

NCT06002919

Conditions

Stress, Psychological

Cognitive Decline

Eligibility Criteria

Sex: All

Age: 45+

Healthy Volunteers: Not accepted

Interventions

MindWalk Intervention

Study Details

Brief summary:

Older South Asian family caregivers experience elevated psychological stress and limited physical activity (PA) due to caregiving responsibilities and additional factors such as lack of access to services, cultural/linguistic barriers, stigma and discrimination. South Asian family caregivers are especially underserved and are a growing ethnic group in the US. Both PA and cognitive training (CT) have shown to improve cognitive function in older adults who experience cognitive function decline because of psychological stress. However, there are no studies using this approach for this population. We propose a randomized control trial pilot study to address this gap. Driven by a Community Advisory Committee (CAC) we will develop this 12-week mindful walking intervention using a participatory methodology in partnership with UIC's Cognition Behavior and Mindfulness Clinic that combines the PA of walking and the CT through mindfulness. We will recruit fifty participants and will randomly and equally assign 25 people to the intervention and 25 people to the control group. The intervention will include: 1) a mindful walking training followed by 2) a prescribed mindful walking regimen, 3) self-reporting of adherence to regimen by the participants using activity logbooks and use of a user-friendly PA tracker (Fitbit) for daily step count, and 4) personalized text messages with reminders and motivational messages for participants to do the mindful walking as prescribed including a weekly check-in call or text message for accountability. The primary aim of the proposed pilot study is to evaluate the feasibility and acceptability of the protocol and intervention implementation. A secondary aim will evaluate the intervention to examine preliminary efficacy in reduction of psychological stress, improvement in cognitive function, increase in physical activity, and increased self-efficacy (self-efficacy for coping with stress, self-efficacy for physical activity, and overall self-efficacy). The findings of this pilot project will provide evidence-based data to support a larger scale study proposal for future funding such as the National Institute on Disability, Independent Living, and Rehabilitation Research (NIDILRR) field initiative award, or the National Institute of Health (NIH) Research Project Grant (R21 NIH Exploratory/Developmental Research Grant Award) award, especially National Institute on Aging (NIA) grants.

Conditions

Stress, Psychological

Cognitive Decline

Study ID

NCT06002919

Start date

Oct 31, 2023

Status verified date

Apr, 2026

Completion date

Dec 31, 2026

Anticipated

Primary completion date

Dec 31, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 45+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Older South Asian family caregivers (45 years or older) caring for a person with cognitive disability of any age
  • Self-reported insufficient physical activity (defined as participating in moderate physical activity less than 60 min/week) and not engaged in mindfulness training
  • Self-reporting of experiencing psychological stress;
  • Own a smartphone with a data plan or Bluetooth-enabled device (e.g., tablets such as iPad) to sync data from the Fitbit tracker to the Fitbit app and to receive text messages
  • Ability to speak, understand, read and write English; ability to provide informed consent

Exclusion Criteria:

  • Non-South Asian caregivers
  • Caregivers less than 45 years old
  • Having self-reported sufficient physical activity (defined as participating in moderate physical activity more than 60 min/week) and engaged in some form of mindfulness training
  • Not owning a smartphone with a data plan or Bluetooth-enabled device (e.g., tablets such as iPad)
  • Mobility limitation
  • Taking medications or other behavioral treatment for stress reduction; acute or chronic diseases at baseline
  • Inability to understand, speak, read, and write English
  • Inability to provide informed consent

Study Design

Enrollment

50 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Other

Interventions and Outcome Measures

Arms

active comparator: MindWalk Intervention

12 week intervention: 1) a mindful walking training followed by 2) a prescribed mindful walking regimen, 3) self-reporting of adherence to regimen by the participants using activity logbooks and use of a user-friendly PA tracker (Fitbit) for daily step count, and 4) personalized text messages with reminders and motivational messages for participants to do the mindful walking as prescribed including a weekly check-in call or text message for accountability.

no intervention: Control group

The participants in the control group will be provided with psychoeducation materials on benefits of walking without any components of mindfulness. The control group will receive neutral text messages with identical frequency and amount of messages that do not include motivational content or reminders related to mindful walking. At the end of study, the control group will also be given access to the recorded virtual mindful walking training (this includes the 30 minutes introductory training and the weekly 10-minute mindfulness topics/modules).

Interventions

MindWalk Intervention

The intervention will include: 1) a mindful walking training followed by 2) a prescribed mindful walking regimen, 3) self-reporting of adherence to regimen by the participants using activity logbooks and use of a user-friendly PA tracker (Fitbit) for daily step count, and 4) personalized text messages with reminders and motivational messages for participants to do the mindful walking as prescribed including a weekly check-in call or text message for accountability.

Primary outcome measure

  • Perceived Stress using the Acceptance and Action Questionnaire-II (AAQ-II) [ Time Frame: Baseline, After 12 weeks and at follow up (20weeks) ]
  • Visuospatial inhibitory attention Using the NIH Toolbox Flanker Inhibitory Control and Attention Test [ Time Frame: Baseline, After 12 weeks and at follow up (20weeks) ]
  • Executive Functioning Using the NIH Toolbox Dimensional Change Card Sort Test [ Time Frame: Baseline, After 12 weeks and at follow up (20weeks) ]

Central Contacts and Locations

Central contacts

Locations

American Association of Retired Asians

Recruiting

Bolingbrook, Illinois, United States, 60440

Contacts

Nazneen Saylawala

nsayla@gmail.com

Sanjeevani 4U

Recruiting

Buffalo Grove, Illinois, United States, 60089

Contacts

Northwestern University

Recruiting

Chicago, Illinois, United States, 60611

Contacts

Apna Ghar

Recruiting

Chicago, Illinois, United States, 60613

Contacts

Radhika Sharma

rsharma@apnaghar.org

South Asian American Policy & Research Institute

Recruiting

Chicago, Illinois, United States, 60640

Contacts

Shobhana Johri Verma

shobhana@saapri.org

Metropolitan Asian Family Services

Recruiting

Chicago, Illinois, United States, 60659

Contacts

Hamdard Health Alliance

Recruiting

Chicago, Illinois, United States, 60660

Contacts

IL Department of Aging

Recruiting

Chicago, Illinois, United States, 60661

Contacts

More Information

Sponsor

University of Illinois at Chicago

Last update posted

May 1, 2026

Last verified

Apr, 2026

Keywords

  • Caregiver of a person with cognitive disability
  • Perceived psychological stress
  • Cognitive Function
  • Mindful Walking
  • Physical Activity
  • Self-efficacy

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-08. This information was provided to ClinicalTrials.gov by University of Illinois at Chicago on 2026-05-01.