Brief Physical Activity Intervention for Older People With Multimorbidity

NCT ID: NCT05287932

Last Updated: 2022-09-27

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

16 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-05-09

Study Completion Date

2022-08-31

Brief Summary

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Physical activity is an important determinant of health and well-being in older people. However, many older people do not achieve recommended physical activity levels and increasing older people's physical activity is challenging. This preliminary study will explore the effects of a brief physical activity intervention on physical activity and physical function in older people with multimorbidity. The findings will be used to inform the design of a subsequent adequately-powered randomised controlled trial.

Detailed Description

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Conditions

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Chronic Conditions, Multiple Old Age; Debility Physical Inactivity

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Pilot randomised controlled trial
Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors
Outcome assessors will be blinded to group allocation, and participants will be asked to not disclose their allocation

Study Groups

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Intervention

Brief physical activity intervention including an initial 45-minute physical activity consultation, telephone support after 2 weeks (approx. 15-minute call), and provision of a pedometer, written information, and a physical activity diary. Embedded behaviour change techniques will include goal setting, self-monitoring, building self-efficacy and social support, and overcoming barriers.

Group Type EXPERIMENTAL

Brief physical activity intervention

Intervention Type BEHAVIORAL

See arm/group descriptions

Wait-list control

The control group will not receive any active or placebo intervention during the 4-week study period. They will also not receive any trial contacts during this period. They will however continue to be able to access their usual care from primary, secondary, community, and social services. After the final (4-week) follow-up assessment, this group will receive the full physical activity intervention.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Brief physical activity intervention

See arm/group descriptions

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* aged ≥60 years
* 2 or more chronic conditions
* able to walk outside the home
* able to attend the study visits

Exclusion Criteria

* living in a residential or nursing home
* housebound
* ≥3 falls in previous year
* dementia or significant cognitive impairment (unable to follow simple instructions)
* contraindication to increasing physical activity
* unable to read or speak English
* unable to provide consent
* no more than one person per household
Minimum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Northumbria University

OTHER

Sponsor Role lead

Responsible Party

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Garry Tew

Professor Garry Tew

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Garry A Tew, PhD

Role: PRINCIPAL_INVESTIGATOR

Northumbria University

Locations

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Northumbria University

Newcastle, , United Kingdom

Site Status

Countries

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United Kingdom

Other Identifiers

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HLSGT030322

Identifier Type: -

Identifier Source: org_study_id

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