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Occupational Impacts of Resistance Training in Older Adults

Occupational Impacts of Compound Resistance Training in Community-Dwelling Older Adults

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07323212
Enrollment
6
Registered
2026-01-07
Start date
2025-08-18
Completion date
2025-11-21
Last updated
2026-01-07

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

Conditions

Older Adults (65 Years and Older), Resistance Training

Brief summary

This study aims to assess the impact of compound resistance training on the ability of adults age 65 and older to participate in desired daily activities, their satisfaction with their level of participation, and their overall mental health.

Detailed description

Eligible and consented participants will complete pre-assessment questionnaires: the Patient Health Questionnaire-9, the Perceived Stress Scale-10, and the Canadian Occupational Performance Measure. Participants will also engaged in a semi-structured interview with pre-set questions. Following pre-assessment, all data will be coded and stored in encrypted software through the university. Participants will then engage in a 10-week intervention period consisting of two 1-hour sessions strength training with principal investigator guiding participants for safety, form, intensity, and volume of exercises. Modifications will be made to exercise programming based on individual performance and individual needs, in accordance with occupational therapy best practices. Rate of Perceived Exertion (RPE) will be used as a guide for intensity with the aim being self-reported RPE 7-8 for each exercise. At completion of the intervention period, participants will complete post-assessment questionnaires: the Patient Health Questionnaire-9, the Perceived Stress Scale-10, and the Canadian Occupational Performance Measure. Participants will also engaged in another semi-structured interview with pre-set questions. Data will be analyzed for statistical and clinically significant changes.

Interventions

OTHERCompound Resistance Training

Intervention will take place over the course of 10 weeks, with individual sessions occurring twice weekly for one hour per session with each participant. Each session will consist of personalized strength training sessions, utilizing programming with a focus on compound, multi-joint movements, in keeping with existing literature on the subject.

Sponsors

Washington Regional Medical Center
CollaboratorOTHER
University of Arkansas
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

Quasi-experimental pre-test post-test

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Adult age 65 or older * Living independently in a community dwelling, such as a house or apartment * Able to complete basic daily tasks (i.e. dressing, toileting, transfers) without assistance from another person * Access to transportation to and from sessions for this study * Able to attend two, one-hour sessions per week for the duration of the study * Has a membership to Silver Sneakers, Silver and Fit, and/or Renew Active, or are willing to obtain a paid membership to Washington Regional Center for Exercise

Exclusion criteria

* · Personal history of stroke or heart attack * Limb amputation * Heart failure or arrythmias * Presence of brain or aortic aneurism * Active cancer * Major illness * Physical activity contraindicated as instructed by a physician * Active drug abuse * Moderate to severe cognitive impairment

Design outcomes

Primary

MeasureTime frameDescription
Canadian Occupational Performance MeasureBaseline and 10 weeksOccupational therapy questionnaire Section 1: Performance Participants requested to report their perception of their performance of a given occupation/activity/daily task on a scale of 1 to 10, with 1 being unable to do it at all and 10 being able to do it with no issues at all. Section 2: Satisfaction Participants requested to reported their satisfaction with their currently level of performance with the previously reported occupation/activity/daily task on a scale of 1 to 10, with 1 being completely dissatisfied and 10 being completely satisfied. Higher scores on either or both sections indicate a better outcome.
Patient Health Questionnaire-9Baseline and 10 weeksMental health questionnaire (depression screen) Participants asked to report the frequency of depression symptoms listed on form over the last 2 weeks using a scale from 0 to 3. Reporting 0 indicates not at all, reporting 1 indicates several days, reporting 2 indicates more than half the days, reporting 3 indicates nearly every day. Lower scores indicate a better outcome
Perceived Stress Scale-10Baseline and 10 weeksMental health questionnaire (stress screen) Participants asked to report frequency of stress impacts on daily life by responding how many days in the past month the participant felt or thought a certain way. Answers are on a scale of 0-4. Reporting 0 indicates never, reporting 1 indicates almost never, reporting 2 indicates sometimes, reporting 3 indicates fairly often, and reporting 4 indicates very often. Lower scores indicate better results.
Reported perceptions of exercise, self-confidence, and confidence in gym environmentbaseline and 10 weeksQualitative data: word associations, open responses, takeaways from study. Thematic analysis and coding for frequency of themes

Countries

United States

Outcome results

None listed

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