Protocol for a Low Threshold Exercise Intervention for Women Experiencing Homelessness and Addiction.

NCT ID: NCT06264895

Last Updated: 2024-05-10

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

ACTIVE_NOT_RECRUITING

Clinical Phase

NA

Total Enrollment

45 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-02-26

Study Completion Date

2024-07-31

Brief Summary

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Background: Frailty is a complex multi-dimensional state of increased vulnerability to adverse health outcomes and is usually associated with older age but there is growing evidence of accelerated ageing and frailty in non-geriatric populations, including those experiencing socio-economic deprivation and extreme social exclusion, such as people experiencing homelessness. Addiction, as a coping mechanism for prior trauma, is common among people who are homeless and can have a gendered dimension. Women experiencing homelessness and addiction have unique needs which require a gendered approach. The aim of this study is to explore the effectiveness of an exercise intervention to target the known physical functioning deficits and frailty which this population experiences.

Methods: This mixed-methods study will explore physical functioning deficits and frailty in women experiencing homelessness and addiction, using a bespoke test battery and an exercise intervention. Physical function (10m Walk Test, 2 Minute Walk Test, Single Leg Stance Test, Chair Stand Test, hand grip dynamometry), frailty (Clinical Frailty Scale and the SHARE-FI) and nutritional status (Mini-Nutritional Status), pain (Numerical Pain Rating Scale) and quality of life (SF 12-V2) will be evaluated. The intervention will involve a 3-times weekly exercise programme with protein supplementation for 10 weeks. Following this, qualitative interviews, which will be thematically analysed using Braun \& Clarke methodology, will be conducted. This study will be conducted in Dublin from February to July 2024.

Discussion: Little is kn own about frailty-focussed interventions in women experiencing homelessness and addiction. This proposed study will help to increase the knowledge base regarding the physical health burden and frailty experienced by this extremely vulnerable population and will deliver a targeted intervention with a gendered dimension to mitigate its affects. The findings of this research will help narrow this research gap and will guide clinicians and policy makers to implement unique gender-based treatment strategies for this population.

Detailed Description

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Previous linked research of exercise interventions in people experiencing homelessness, demonstrated high retention with excellent engagement and feedback from its female participants, yet caution was observed around engaging in a mixed exercised programme with men. Women have traditionally been underserved in research and policy, yet multiple sources cite women as the fastest growing homeless demographic. No study has examined how targeted women-only exercise programmes with nutritional supplementation work in practice in this population.

The overall aim of this study is to explore physical functioning and frailty outcomes of an exercise intervention with protein supplementation in a group of (non-geriatric) women experiencing homelessness and addiction challenges.

The objectives are:

1. To evaluate recruitment, retention and adherence rates, and any adverse effects of the intervention.
2. To evaluate pre- and post-intervention levels of physical, nutritional and frailty status, pain and general health status.
3. To evaluate programme feedback and gain deeper insights into participants perspectives and experiences of the exercise intervention.

This mixed-methods study will involve a single-arm intervention which will take place in Dublin city centre, in a day-service centre which provides services for women who are homeless and/or in addiction. Following the intervention qualitative research in the form of individual exit interviews will be conducted with 20 participants or up to the point of data saturation.

The 10-week intervention will involve a low threshold, three-times weekly exercise programme (two exercise classes with protein supplementation and an outdoor 'Park Walk') delivered over 12 weeks to offer flexibility to participants. It will be delivered by two research physiotherapists who will adhere to all safety procedures. Further flexibility will be facilitated with the provision of a four-week window for pre-intervention evaluations prior to commencement of the programme, and group or one-to one sessions will be delivered based on participant preference. The exercise classes will be multi-modal, with a primary focus on strength and based on core set of resistance exercises. Aerobic, balance and flexibility work will be integrated into the class and the exercises will be individualised based on initial assessment results and presentation of participants. Using a gender-based perspective, the following considerations and adaptions will be built into the class; (i) core-stability exercises to target pelvic floor and/or abdominal muscle weakness, (ii) bone building exercises to target peri-and postmenopausal bone loss and (iii) age-associated muscle mass loss. Music, dance and fun orientated physical activity games, an important feature of prior linked studies, will be incorporated to optimize enjoyment and self-esteem. Borg's Rate of Perceived Exertion Scale will be used to monitor effort and scale the intensity of the workout. To promote post-exercise muscle protein synthesis, a nutritional supplement (200ml pre-prepared 'protein shake', Fresubin) which consists of 20g of protein will be offered immediately post exercise. The 'Park Walk' will focus on the aerobic component of the intervention, using green open space to maximise physical and mental health outcomes. It will be a flexibly arranged 20-30 minute self-paced group or one-to-one walk. To build sustainability beyond the ten week programme brief health promoting and physical activity educational interventions will be included in the exercise class setting to empower people to engage in unsupervised exercise following the study. Following the intervention one-to-one in-person exit interviews will be conducted to enable participants to provide feedback and express personal views, in order to enhance the understanding of behaviours, adherence and retention challenges and to provide insights for future programmes in this area. Interviews will continue until 20 participants are seen or until data saturation is reached. The interviews will be audio-recorded and transcribed verbatim and member checking will be utilised.

Analytic plan: For quantitative data, nominal or ordinal variables will be reported as frequencies and percentages. Continuous variables will be summarised as mean and standard deviation if normally distributed and median and inter-quartile range if non-normally distributed. Data will be tested for normality using the Kolmogorov-Smirnov/Shapiro Wilk test and will be compared across timepoints using the general linear model procedure (normally distributed data) and the Friedman's test (non-normally distributed data). Chi-squared t-tests will be used where appropriate and some data may be categorised to investigate relationships between variables. Exploratory regression models will be developed to explore correlates and predictors of frailty and poor physical functioning. A p-value of \<0.05 will be considered significant. For the qualitative data, Braun and Clarke thematic analysis methodology will be employed to provide an in-depth analysis of the exit interview data.

Conditions

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Social Exclusion Chronic Disease Physical Disability Addiction

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

single -arm longitudinal cohort study
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Evaluation of an exercise intervention for women experiencing homelessness and addiction.

A 3 times weekly exercise intervention with protein supplementation will be delivered to all study participants for 10 weeks.

Group Type EXPERIMENTAL

Exercise

Intervention Type BEHAVIORAL

three times weekly exercise intervention with protein supplementation

Interventions

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Exercise

three times weekly exercise intervention with protein supplementation

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Adult women (18-65 years) accessing services in Jane's Place who consent to participation.

Exclusion Criteria

* Any person not meeting the age eligibility criteria.
* Any person identifying as a male.
* Any person lacking capacity to give consent.
* Any person with major physical/medical or cognitive challenges which would preclude ability to safely complete the assessment or
* Any person with insufficient English language ability to give fully informed consent.
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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University of Dublin, Trinity College

OTHER

Sponsor Role lead

Responsible Party

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Julie Broderick

Dr. Julie Broderick, Assistant Professor, Head of Discipline of Physiotherapy

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Julie Broderick, PhD

Role: PRINCIPAL_INVESTIGATOR

Trinity College, University of Dublin, Dublin, Ireland

Locations

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Trinity College Dublin, University of Dublin

Dublin, , Ireland

Site Status

Countries

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Ireland

Other Identifiers

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Trinity College Dublin 211202

Identifier Type: -

Identifier Source: org_study_id

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