- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07312331
SOC-based Behavioral Intervention to Promote Walking (SOCWalk)
December 17, 2025 updated by: Ling Yang
SOC-based Behavioral Intervention to Promote Walking and Well-being Among Older Adults in Jiazhou, China
Drawing on the Selection, Optimization, and Compensation (SOC) model of adaptive development, this study tested whether a structured behavioral intervention could enhance walking activity and well-being through improvements in self-regulatory strategy use.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
350
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Henan
-
Jiaozuo, Henan, China, 454099
- Henan Polytechnic University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Individuals were excluded if they had moderate-to-severe cognitive impairment, medical contraindications for walking, or planned relocation within six months.
Exclusion Criteria:
- Eligible participants were Chinese adults aged 65 years or older, lived in urban areas, could walk independently for at least 10 minutes, and had access to a mobile phone or WeChat (personally or through a family member).
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: SOC
SOC-based walking intervention
|
A structured Selection, Optimization, and Compensation (SOC)-based workshop designed to promote adaptive self-regulation in the domain of physical activity, particularly walking
|
|
Active Comparator: Active control group
active health education control.
|
A general health education program that covered age-related topics such as nutrition, sleep, medication adherence, and mental well-being, but excluded any self-regulatory or goal-setting components.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Walking behavior
Time Frame: From enrollment to the end of treatment at 8 weeks
|
weekly minutes of walking
|
From enrollment to the end of treatment at 8 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Selection
Time Frame: From enrollment to the end of treatment at 8 weeks
|
Use of "SOC (Selection, Optimization, and Compensation strategies)" questionnaire specific to walking, assessed with brief subscales (3-4 items each; 5-point Likert), at T0, T1, and T2.
It assesses the self-regulatory strategies using a 12-item version of the Selection Questionnaire originally developed by Freund and Baltes (2002) and validated for use with Chinese older adults by Chou and Chi (2001).
The instrument comprises three subscales-in this case we use the Selection scale-with four items rated on a 5-point Likert scale (1 = strongly disagree, 5 = strongly agree).
|
From enrollment to the end of treatment at 8 weeks
|
|
Optimization
Time Frame: From enrollment to the end of treatment at 8 weeks
|
Use of SOC "Selection, Optimization, and Compensation strategies Questionnaire" specific to walking, assessed with brief subscales (3-4 items each; 5-point Likert), at T0, T1, and T2.
For this outcome, we use the subscale Optimization, which self-regulatory strategies assessed using a list of Optimization items, originally developed by Freund and Baltes (2002) and validated for use with Chinese older adults by Chou and Chi (2001).
The instrument comprises is rated on a 5-point Likert scale (1 = strongly disagree, 5 = strongly agree).
|
From enrollment to the end of treatment at 8 weeks
|
|
Compensation
Time Frame: From enrollment to the end of treatment at 8 weeks
|
Use of SOC "Selection, Optimization, and Compensation strategies Questionnaire" specific to walking, assessed with brief subscales (3-4 items each; 5-point Likert), at T0, T1, and T2.
We use the Compensation subscale of self-regulatory strategies, that was originally developed by Freund and Baltes (2002) and validated for use with Chinese older adults by Chou and Chi (2001).
The instrument is rated on a 5-point Likert scale (1 = strongly disagree, 5 = strongly agree).
|
From enrollment to the end of treatment at 8 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 1, 2025
Primary Completion (Actual)
June 30, 2025
Study Completion (Actual)
June 30, 2025
Study Registration Dates
First Submitted
November 25, 2025
First Submitted That Met QC Criteria
December 17, 2025
First Posted (Actual)
December 31, 2025
Study Record Updates
Last Update Posted (Actual)
December 31, 2025
Last Update Submitted That Met QC Criteria
December 17, 2025
Last Verified
December 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- SOCWALK2025
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
The protection of the privacy of our respondents does not allow us to share IPD.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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