Skip to main content
OpenTrials
Completed

NCT Number: NCT07323212

Occupational Impacts of Resistance Training in Older Adults

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.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Resistance Training Older Adults (65 Years and Older)

Age range

65 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Washington Regional Center for Exercise

Fayetteville, Arkansas, 72703, United States

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Compound Resistance Training

Other

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.

Primary outcomes

  1. Canadian Occupational Performance Measure

    Time frame: Baseline and 10 weeks

    Occupational 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.

  2. Patient Health Questionnaire-9

    Time frame: Baseline and 10 weeks

    Mental 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

  3. Perceived Stress Scale-10

    Time frame: Baseline and 10 weeks

    Mental 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.

  4. Reported perceptions of exercise, self-confidence, and confidence in gym environment

    Time frame: baseline and 10 weeks

    Qualitative data: word associations, open responses, takeaways from study. Thematic analysis and coding for frequency of themes

Sponsors and collaborators

Lead sponsor

University of Arkansas

Other

Collaborators

  • Washington Regional Medical Center

Registry information

Official study title

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

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Jan 7, 2026
Registry last updated
Jan 7, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Related clinical trials

Published trials that share one or more normalized conditions with this study.