Evaluation of Two Different Delivery Approaches of a GP Exercise Referral Scheme

March 31, 2016 updated by: Paula Watson, Liverpool John Moores University

Theory-informed Evaluation of Two Delivery Approaches of a GP Exercise Referral Scheme

Physical activity (PA) benefits both physical and psychological health, yet the majority of UK adults are physically inactive. "Exercise for Health" (EFH) is a General Practitioner (GP) exercise referral scheme run in Liverpool for people who are inactive with a medical condition. Patients are referred by their GP practice, where they receive 12 weeks of subsidised exercise classes at their local leisure or community centre.

In 2012, one of the thirteen EFH centres (Centre A) introduced some changes to try and improve EFH at their centre. These changes included:

  • a pre-scheme meeting with a health trainer, to help the patient decide if EFH is for them.
  • exclusive classes (gym or activities) available daily for EFH participants (compared to gym only classes two or three times a week in other centres).

This non-randomised study will compare the effectiveness of the adapted EFH (Centre A) with standard EFH delivery (Centre B). All participants referred to centre A (n=100 approx) or centre B (n=100 approx) during the study period will be invited to take part. Changes in self-reported PA, PA self-efficacy and psychological wellbeing will be measured at the end of EFH (12 weeks) and at 12-month follow-up. A subsample of participants (n=15 from each centre) will take part in qualitative interviews to explore the factors that contribute to effectiveness.

A secondary aim is to explore psychological factors contributing to any differences between the two centres. Self-determination theory suggests that where participants feel they are offered choice, feel they are competent at exercise, and feel connected to people they exercise with, they will be more intrinsically motivated and more likely to continue exercising. Therefore it is hypothesised that participants attending the adapted EFH will be more motivated and more likely to continue exercising.

Study Overview

Detailed Description

This mixed-method observational study will compare the short- and long-term effectiveness of two different delivery approaches of an exercise referral scheme (Exercise for Health, EFH). As the intervention is already in widespread use randomisation is not feasible, therefore a case control design is adopted to compare the effectiveness of an adapted EFH scheme (delivered at centre A) with the standard EFH scheme (delivered at centre B). Centre B is selected as the comparison centre due to its similarity to centre A on socio-demographic markers (e.g. number of EFH referrals, socioeconomic make-up of local population).

Although the adapted scheme has not drawn overtly from Self-determination Theory (SDT), it is hypothesised that the adapted scheme promotes greater environmental support of SDT-based psychological needs for participants than the standard EFH scheme. Autonomy is promoted through the increased choice offered through daily sessions and the involvement of the patient in their decision whether to take up the scheme, competence is encouraged through the tailoring of classes to the ability of EFH participants and the opportunity to observe similar others, and relatedness is supported through the social assimilation of participants through regular group activities.

It is hypothesised that:

  1. Both EFH delivery approaches will have beneficial effects on participants' self-reported PA, self-efficacy and psychological well-being post-intervention.
  2. Participants attending the adapted scheme will perceive greater needs support, greater psychological needs satisfaction and more autonomous motivation during and post-intervention; will have higher adherence to EFH; will have higher leisure centre attendance from post-intervention to 12 months and report higher PA levels at 12 months.
  3. Perceived needs support will predict psychological needs satisfaction during the intervention; psychological needs satisfaction during the intervention will predict autonomous motivation and psychological well-being post-intervention; post-intervention autonomous motivation will predict PA at 12 months and leisure centre attendance from post-intervention to 12 months.

Study Type

Observational

Enrollment (Actual)

202

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Merseyside
      • Liverpool, Merseyside, United Kingdom, L3 2AT
        • Liverpool John Moores University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

16 years and older (ADULT, OLDER_ADULT, CHILD)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Inactive adults (16+ years) who have, or are at risk of developing, a medical condition (e.g. hypertension, obesity, depression).

Description

Inclusion Criteria:

  • Individuals attending an EFH induction at centre A or centre B during the recruitment period (anticipated to be between May and July 2014).

Exclusion Criteria:

  • Participants with an insufficient level of English language to understand the participant information sheet (in written or spoken format).

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Adapted scheme
Participants referred by their GP practices to Centre A will take part in the Adapted Exercise for Health (EFH) scheme.

12-week subsidised exercise programme at local authority-run leisure centres. Each participant receives a programme of activities tailored to their needs, based on a standard recommendation of two exercise sessions per week. In February 2012, Centre A introduced some changes to the EFH scheme as follows:

  • Pre-scheme meeting with a health trainer to help the patient decide if EFH is for them.
  • Participants offered specially tailored group classes (exclusive to EFH participants, e.g. low-impact circuits, Zumba) as well as access to the main gym.
  • Opportunities to attend daily.

Although subsidised access to mainstream group classes and swim sessions (i.e. includes all leisure centre members) is also available, this option is not openly advertised on the adapted scheme.

Standard scheme
Participants referred by their GP practices to Centre B will take part in the Standard Exercise for Health (EFH) scheme.

12-week subsidised exercise programme at local authority-run leisure centres. Each participant receives a programme of activities tailored to their needs, based on a standard recommendation of two exercise sessions per week.

The scheme includes exclusive EFH gym sessions (i.e. includes EFH participants only) on two to three days of the week, plus subsidised access to mainstream group classes and swim sessions (i.e. includes all leisure centre members).

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in self-reported physical activity (PA)
Time Frame: Baseline, 12 weeks, 12 months
Self-reported PA will be measured using the vigorous PA, moderate PA and walking items of the short version of the International Physical Activity Questionnaire (IPAQ). The short-IPAQ is a 7-day recall self-administered tool that measures intensity, frequency and duration of PA and provides a total estimate of energy expenditure. A total score of MET-minutes/week will be calculated according to the IPAQ scoring protocol, which is available to download from http://www.ipaq.ki.se/ipaq.htm
Baseline, 12 weeks, 12 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in physical activity self-efficacy
Time Frame: Baseline, 12 weeks, 12 months
A two-item measure of PA self-efficacy (SE) was developed to reflect the intervention aims. Item one measures self-efficacy to adhere to the Exercise for Health programme ("how confident are you that you can attend exercise sessions twice a week?"); item two measures self-efficacy to adhere to a physically active lifestyle in general ("how confident are you that you can be moderately physically active for at least 30 minutes on 5 days of the week?"). Participants are asked to rate their confidence on a scale of 0 (not at all confident) to 10 (extremely confident).
Baseline, 12 weeks, 12 months
Change in psychological wellbeing
Time Frame: Baseline, 12 weeks, 12 months
Psychological wellbeing will be measured using the Warwick-Edinburgh Mental Well-being Scale (WEMWBS). WEMWBS is a 14-item positively worded measure containing items related to psychological functioning (e.g. "I've been thinking clearly") and subjective well-being (e.g. "I've been feeling cheerful"). Participants are asked to rate on a likert scale of 1 (none of the time) to 5 (all of the time) how well each statement describes their experiences over the last two weeks.
Baseline, 12 weeks, 12 months
Adherence to the Exercise for Health programme
Time Frame: Between baseline and 12 weeks
Adherence will be expressed as a percentage of the recommended twice weekly leisure centre attendance over 12 weeks.
Between baseline and 12 weeks
Post-intervention leisure centre attendance
Time Frame: Between 12 weeks and 12 months
The number of occasions participants attend either gym sessions, classes or swim sessions between 12 weeks and 12 months will be obtained from computerised attendance records. Two measures will be taken: the absolute number of attendances (regardless of when these occur) and regularity of attendance (i.e. number of months in which participants attend at least once).
Between 12 weeks and 12 months

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Self-determination theory variables
Time Frame: 4 weeks, 12 weeks and 12 months

Needs support (4 weeks and 12 weeks only) will be measured using a 15-item needs support (NS) tool that assesses participant perceptions of the extent to which their exercise referral instructors provide support for autonomy, structure (linked to competence) and involvement (linked to relatedness).

Psychological needs satisfaction will be measured using the Psychological Need Satisfaction in Exercise Scale (PNSE). The PNSE is an 18-item tool designed to measure participants' perceived autonomy, competence and relatedness in an exercise context.

Behavioural regulation of exercise will be measured using the revised Behavioural Regulation in Exercise Questionnaire (BREQ-2), which contains 19 items exploring reasons why people exercise. The scale includes items measuring amotivation, external regulation, introjected regulation, identified regulation and intrinsic motivation of exercise behaviour. Four additional items will be included to assess integrated regulation.

4 weeks, 12 weeks and 12 months
Qualitative interviews
Time Frame: 4 weeks and 12 months

Qualitative interviews with a randomly-selected subsample of participants (15 per centre) will explore the following research questions:

  • What are the facilitators and barriers to exercise adoption for Exercise-for-Health (EFH) participants?
  • How acceptable is EFH to participants and how could it be improved?
  • How well do the processes of referral, induction and EFH activities at each centre support participants' perceived needs for autonomy, competence and relatedness?
  • What factors (EFH and individual) facilitate PA maintenance at 12 months?
4 weeks and 12 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

May 1, 2014

Primary Completion (ACTUAL)

December 1, 2015

Study Completion (ACTUAL)

December 1, 2015

Study Registration Dates

First Submitted

May 16, 2014

First Submitted That Met QC Criteria

May 16, 2014

First Posted (ESTIMATE)

May 20, 2014

Study Record Updates

Last Update Posted (ESTIMATE)

April 1, 2016

Last Update Submitted That Met QC Criteria

March 31, 2016

Last Verified

March 1, 2016

More Information

Terms related to this study

Other Study ID Numbers

  • SPS-14-01
  • 14/YH/0160 (OTHER: National Research Ethics Service)

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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