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MI for Physical Activity Among Older Adults

Motivational Interviewing for Physical Activity Among Older Adults

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05179148
Enrollment
7
Registered
2022-01-05
Start date
2022-03-23
Completion date
2023-03-30
Last updated
2022-12-12

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

Conditions

Motivational Interviewing

Keywords

motivational interviewing, physical activity, older adults, virtual

Brief summary

The purpose of this study is to determine the feasibility of VIrtual Motivational INTerviewing (VIMINT) to promote physical activity levels among older adults; post-intervention and at two-month follow-up.

Detailed description

Evidence shows that moderate and regular physical activity is associated with the prevention of non-communicable diseases, increased bone density, reduced risk of dementia, and prevention of falls among older adults. Despite the numerous benefits of physical activity, many older adults do not meet the recommended physical activity guidelines of 150 min/week of moderate-to-vigorous intensity physical activity in Canada. MI is a client-centered counselling style for strengthening a person's own motivation and commitment to change. MI helps evoke the person's own motivation for changes through reflective listening, engaging, evoking, and planning. MI has shown to be promising in the general adult population for improving physical activity levels, however, there were mixed results for the effectiveness of MI among older adults. In addition, based on the available evidence, there are no studies evaluating the potential long-term effects of MI on physical activity levels among older adults. This feasibility study is necessary to explore possible challenges that may be encountered in the future larger trial with a two-month follow-up. Due to the recent pandemic (COVID-19), the intervention will be conducted virtually through the videoconferencing platform (Zoom). Therefore, the purpose of this study is to determine the feasibility of VIrtual Motivational INTerviewing (VIMINT) to promote physical activity levels among older adults; post-intervention and at two-month follow-up. The participants will receive five sessions of the virtual MI over a five-week period through the Zoom platform and each session will last between 45 to 60 minutes. The intervention will be delivered by trained personnel in MI. The MI strategies will include evoking change and guiding participants in establishing goals for improving physical activity. After the 2-month evaluation, counsellors and participants will be invited for a one-on-one Zoom interview. The aim is to explore the perception of the counsellors and participants about the VIMINT study including, views about virtual MI, benefits, and challenges.

Interventions

BEHAVIORALMotivational Interviewing

MI is a client-centered counselling style for strengthening a person's own motivation and commitment to change. MI helps evoke the person's own motivation for changes through reflective listening, engaging, evoking, and planning

Sponsors

University of Manitoba
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* aged 65 years or older * living in the community * able to walk with or without mobility aid for at least 10 metres * physically inactive i.e., less than 150 minutes of moderate-vigorous intensity * ready to participate in physical activity and no medical concerns using the Physical Activity Readiness Questionnaire (PAR-Q+)\* * score of ≥ 18 on the telephone version of the Mini-mental State Exam * able to speak English * able to have access to a computer, tablet or mobile phone capable of running the videoconferencing platform (Zoom) * able to access internet and email

Exclusion criteria

* • receiving on-going treatment for any medical condition that would prevent safe participation in physical activity * living in long-term care * participating in other behavioural interventions that focus on improving physical activity

Design outcomes

Primary

MeasureTime frameDescription
Total number of participants recruited per monththroughout the study, average of 1 yearThe recruitment rate is the number of participants screened, the number of those who provide written informed consent and the percentage of those who attend the baseline assessment
the percentage of participants that remained after the last data is completed at 1 yearafter completion of data collection at 1 yearTotal number of participants that completed the follow-up assessment at 3 months post-baseline divided by the total number of participants that completed the post-intervention assessment at 1 month post-baseline
the counsellor's competence will be assessed using Motivational Interviewing Treatment Integrity Code 4.2.1 after completing the motivational interviewing counselling at 1 month post-baseline assessmentat 1 month post baselineThe counsellor's competence will be assessed by listening to the audio recorded MI sessions using the global score on the Motivational Interviewing Treatment Integrity Code (MITI 4.2.1.) MITI 4.2.1 consists of four global ratings for the counsellor: cultivating Change talk, Softening Sustain Talk, Partnership, and Empathy. Each of the four global ratings are scored on a five-point Likert scale with 1 and 5 as the lowest and highest proficiency respectively.
participant level of satisfaction will be assessed using the Client Satisfaction Questionnaire version 8 at follow-up assessment which is 3 months post baseline3 months post baselineThe Client Satisfaction Questionnaire version 8 is an 8-item scale that is scored using a Likert from 1 (quite dissatisfied) to 4 (very satisfied). The score ranges from 8 to 32, with a higher score representing higher satisfaction

Secondary

MeasureTime frameDescription
change from baseline in the mean of task self-efficacy physical activity using 10 items from task self-efficacy physical activity questionnaire at 1 month and 3 months post baseline.baseline, 1month and 3 months post baselinethe self-efficacy physical activity questionnaire is a 10-item, participants will be asked to rate their level of confidence on a scale 0 (not at all confidence) and 100 (completely confident). The ratings will be summed and averaged to give a score of task self-efficacy physical activity score.
change from baseline of self-reported light, moderate and vigorous using Community Healthy Activities Model Program for Seniors (CHAMPS) questionnaire at 1 month and 3 monthsbaseline, 1 month and 3 months post baselineCHAMPS is a 41-item questionnaire. We will administer the CHAMPS questionnaire through the Zoom platform at baseline, 1 month, and 3 months post baseline. The participants will be asked to indicate if they engage in an activity, and if the participants indicate NO they will be scored zero. Any activities the participants indicate YES, we will ask how many times they engage in the activity in a week. Afterward, the participants will be asked to select the total hours/week they engage in the activity from the following six categories: less than 1 hr, 1-2½ hrs, 3-4½ hrs, 5-6½ hrs, 7-8½ hrs, and 9 hrs or more. Each activity on the CHAMPS is assigned a Metabolic equivalent (MET) value as recommended by Stewart et al. (2001). We will compute the total hours/week; a MET value of ≥ 3.0 and ≥ 5.0 will be defined as moderate-vigorous and vigorous intensity physical activity respectively.
change from baseline in the readiness of the participant to change behaviour using readiness-to-change ruler at baseline and 1 month post baselinebaseline and 1 month post baselinethe readiness-to-change ruler is an arbitrary line on a scale of 0 to 10 where 0 means Not ready to change, and 10 means Ready to change''. The readiness-to-change ruler helps to gauge the motivational and ambivalence state of an individual. Typically, the scores are interpreted with 0-3 as not ready, 4-7 as ambivalence or not sure and 8-10 as ready for change.
Change from baseline in the total sporadic minutes per day of the light and moderate-vigorous intensity physical activity and total number of steps per day using activity monitor(GT3X+ model) at 1 months and 3 monthsbaseline, 1 month and 3 months post baselineParticipants will be asked to wear the activity monitor on an elastic waistband over the right hip for at least 10 waking hours for seven consecutive days. low frequency extension (LFE) option to capture the various physical activity intensities. The light and moderate-vigorous intensity physical activity will be analyzed using the cut point of 100-759 and ≥760 counts per minute respectively.
Change from baseline in the quality of life using The Research ANd Development-36 (RAND-36) at 1 month and 3 monthsbaseline, 1month and 3 months post baselineRAND-36 is a 36-item generic measure of the HRQoL that assesses eight health concepts: physical functioning (10 items), role limitations due to physical health problem (4 items), role limitations due to emotional problems (3 items), social functioning (2 items), emotional well-being (5 items), energy/fatigue (4 items), pain (2 items), and general health perceptions (5 items). RAND-36 also assesses change in perceived health during the last 12 months using a single item. Each item has different response categories (1-6), which are then transformed to various values as recommended by Hays and Morales (2001). The score ranges between 0 and 100 (SD =10) with a higher score indicating better physical or mental health.
change from baseline in the mean self-efficacy for exercise using 9-item Self-efficacy for exercise questionnaire at 1 month and 3 monthsbaseline, 1month and 3 months post baselineIt is a 9-item instrument with responses ranging from 0 (not confident) to 10 (very confident), and a higher score indicating higher self-efficacy for physical activity or exercise. The scoring is calculated by summing up the total score and dividing by the number of items (nine).

Countries

Canada

Outcome results

None listed

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