Skip to main content
OpenTrials
Completed

NCT Number: NCT03906162

A 12-week Intervention With Motivational Interviewing and Physical Activity Monitoring, to Enhance the Daily Amount of Physical Activity in Community Dwelling Older Adults - a Randomized Controlled Trial

To investigate if motivational-interviewing will enhance the expected effect from physical activity monitors, on physical activity in older adults, we will conduct a two-arm randomized controlled trial in 2019.

Both groups in the trial will receive a physical activity monitor for everyday use in the 12-week intervention period and a folder with information about the benefits of physical activity in older age. Participants in the intervention group will in addition to the use of the physical activity monitors receive a motivational feedback session by phone of about 20 minutes constructed from the theoretical framework of Motivational interviewing by Rollnick, Miller & Butler and Social Cognitive Theory by Bandura. The content of the session focuses on investigating the most relevant possibilities and barriers for the participant to increase his or her levels of PA.

The primary outcome will be between group difference in average steps per day throughout the intervention period, measured objectively by the physical activity monitor (Garmin Vivofit 3). Secondary outcomes include participant reported outcome measures such as 'International Physical Activity Questionnaire', 'Nordic Physical Activity Questionnaire', 'EQ5D Quality of life questionnaire', 'UCLA Loneliness Scale', 'Self Efficacy for Exercise', and 'Outcome expectancy for Exercise'. To ensure 80% power with an alpha-level on 0.05, we will include 128 participants. The study will enroll in March 2019.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Aging Behavior Motor Activity Older Adults Physical Activity

Age range

70 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Rasmus Tolstrup

Copenhagen, 1663, Denmark

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

Participants must:

  • Be minimum 70 years of age at the time of inclusion
  • Own and use an Apple/Google/Microsoft smartphone device compatible with the Garmin Connect™ Mobile application.
  • Own use an e-mail account
  • Live in Denmark and have a Danish postal address and be able to receive the intervention content.
  • Be able to walk independently with or without assistive devices.

Exclusion criteria

Participants cannot

  • Receive active cancer treatment
  • Have major cognitive impairment (e.g. dementia or alzheimers).
  • Parkinson's or Multiple Sclerosis (or similar disease) affecting their mobility in such a way that the participants cannot walk on a daily basis.

Treatment and study plan

Motivational interviews

Behavioral

During the 12-week intervention, the participants will receive seven telephone calls from a physical therapist. The interviews will be held in week 1, 2,3,5,7,9, and 12.

The telephone call will consist of a motivational interview focused on enhancing the daily level of physical activity in the participants.

MI is a form of counselling aiming at prompting increases in self-efficacy, which may leave people more open to and invested in changing their behaviours and shows potential for significant effects for exercise behaviour change.

In addition to the telephone based motivational interviews, the experimental group will also receive the "base intervention" which is described in detail under the "control intervention paragraph".

Base intervention

Behavioral

The "base intervention" consists of a physical activity monitor (PAM) for everyday use in the intervention period and a pamphlet with information about Danish recommendations on physical activity in aging populations. The PAM will be the Garmin Vivofit 3 monitor linked to a pre-specified Garmin Connect account. The participants will be asked to install the Garmin Connect application on their smartphone and use the given ID/password in the app. The participants will be asked to wear the monitor 24-hours a day for the 12-week intervention period. The participants can use the PAM as they like but they will be asked to try to use the PAM and the application to enhance their daily level of physical activity.

Primary outcomes

  1. Individual intervention period average of PAM measured steps per day

    Time frame: A daily average of the 12 weeks of intervention

    Daily step counts will be objectively measured by the PAM.

Secondary outcomes

  1. International Physical Activity Questionnaire

    Time frame: Baseline + end point at 12 weeks + follow up at 6 months and 12 months

    Questionnaire: The seven-item IPAQ-SF measure assesses the types of intensity of physical activity and sitting time that people has done the past seven days as part of their daily lives are considered to estimate total physical activity in MET-min/week and time spent sitting.

  2. Nordic Physical Activity Questionnaire

    Time frame: Baseline + end point at 12 weeks + follow up at 6 months and 12 months

    Questionnaire: It is developed to monitor compliance with the WHO recommendations on PA.

  3. EQ5D Quality of life questionnaire

    Time frame: Baseline + end point at 12 weeks + follow up at 6 months and 12 months

    Questionnaire: The EQ-5D-5L is a generic health-related quality of life (HRQoL) measure developed as a non-disease-specific instrument for describing and valuing health states and comprises five dimensions (mobility, self-care, usual activities, pain/discomfort and anxiety/depression), each of which has three levels (no problems, moderate problems and extreme problems) and a visual analogue scale (EQ VAS). The score for the five dimensions can be combined into a five-digit number that describes the patient's health state. The EQ VAS records the patient's self-rated health on a vertical visual analogue scale, where the endpoints are labelled 'The best health you can imagine' and 'The worst health you can imagine'.

  4. University of California, Los Angeles, Loneliness Scale

    Time frame: Baseline + end point at 12 weeks + follow up at 6 months and 12 months

    Questionnaire: The 20-item UCLA loneliness scale (third version) is a self-report measure of loneliness and social isolation. The scale consists of 11 positive and nine negative items and the total score is calculated by finding the sum of 20 items (0-60), with a higher score indicating more loneliness.

  5. Self Efficacy for Exercise

    Time frame: Baseline + end point at 12 weeks + follow up at 6 months and 12 months

    Questionnaire: The nine-item SEE-DK addresses confidence to engage in regular exercise [44], when challenged by known barriers to exercise. The scale was developed initially for sedentary adults in the community who participated in an outpatient exercise program and was revised to older adults. It is designed to be administered using face-to-face interview. Response categories range from 0 (no confidence) to 10 (very confident). Item scores are used to calculate a total score (0-90), with higher scores indicating higher confidence, or self-efficacy, related to exercise. The SEE-DK is adapted to Danish older adults with acceptable face and content validity, construct validity by acceptable model fit as a unidimensional scale, and test-retest reliability.

  6. Outcome expectancy for Exercise

    Time frame: Baseline + end point at 12 weeks + follow up at 6 months and 12 months

    Questionnaire: The 13-item OEE-2 scale was developed from the original 9-item Outcome Expectations for Exercise scale (OEE) that specifically focused on measuring the positive outcome expectations for exercise (POEE). To complete the OEE2-DK scale the participants are asked, using a Likert scale, to strongly agree, agree, neither agree nor disagree, disagree, or strongly disagree with the stated outcomes to each statement of exercising.

Sponsors and collaborators

Lead sponsor

University of Copenhagen

Other

Registry information

Acronym: MIPAM

Important dates

Study start
2019
Primary completion
2020
Study completion
2020
First posted
Apr 8, 2019
Registry last updated
Oct 8, 2020

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.