About this trial
Achilles tendinopathy is a common condition that causes pain and stiffness in the tendon at the back of the ankle. It can make walking, exercise, work, and everyday activities difficult. The main recommended treatment is a programme of progressive tendon-loading exercises, usually supported by an NHS physiotherapist. These exercises can help improve pain and function, but many people find them hard to continue over time. This means that, even though the treatment can work well, some people do not get the full benefit because they are unable to keep up with the exercise programme as advised.
People with Achilles tendinopathy often describe worries about making the tendon worse, uncertainty about whether pain during exercise is safe, low confidence, slow progress, and difficulty fitting exercises into daily life. These challenges may be even greater for people from underserved groups, including those living with long-term health conditions, financial pressures, language barriers, or other forms of disadvantage. At present, there is limited research exploring these experiences in a structured way, especially in routine NHS care.
The aim of this study is to understand what helps or makes it harder for people to stick with NHS-prescribed progressive tendon-loading exercises for Achilles tendinopathy. The study will focus particularly on the experiences of people who may be at higher risk of poor outcomes or reduced access to support.
Up to 30 adults with experience of Achilles tendinopathy and previous NHS physiotherapy treatment will take part in a one-to-one interview. Interviews will last up to 45 minutes and can take place in person, online, or by telephone, depending on what suits the participant best. Participants will be asked about their experiences of living with Achilles tendon pain, being given exercise treatment, and trying to follow that treatment in everyday life.
The information from these interviews will be analysed to identify the main barriers and supports affecting exercise adherence. The findings will be used to build a clearer understanding of the behavioural factors that influence whether people are able to continue with treatment. This will help inform the future development of a targeted support approach to improve adherence to exercise-based rehabilitation for Achilles tendinopathy in NHS practice.
The long-term goal of the study is to help make treatment more effective, more personalised, and more suitable for people from a wide range of backgrounds, including those whose needs are often overlooked in research and healthcare design.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
• Adults aged 18 years or over with lived experience of Achilles tendinopathy (AT).
Gender representation: A purposive sample including men and women, with inclusion of non-binary participants where self-identified, aiming for broad gender representation rather than fixed quotas.
Ethnic and cultural diversity: Purposive sampling will seek representation from diverse ethnic and cultural backgrounds, informed by local population demographics and service user profiles.
Socioeconomic diversity: Participants will be recruited across high, mid, and low socioeconomic deprivation groups, defined using postcode-derived Index of Multiple Deprivation (IMD) tertiles (lower, middle, upper thirds of national IMD distribution). Recruitment will aim for representation across all three IMD categories rather than predefined percentages.
Disqualifiers
• Under 18 years of age
Inability to confirm previous AT through either ELHT electronic medical records or through discussion with CI
Individuals whose Achilles symptoms are due to a different primary pathology (e.g., Rheumatological, Achilles Rupture)
Unable to provide informed consent
Trial population
The study population will comprise adults aged 18 years and over with lived experience of Achilles tendinopathy who have previously received, and attempted to follow, an NHS-prescribed progressive tendon-loading exercise programme within the past 24 months. Participants will be recruited from NHS musculoskeletal service records, community engagement routes, and individuals who have previously expressed interest in Achilles tendon research. The study will use purposive sampling to achieve diversity in age, gender, ethnicity, socioeconomic background, and clinical characteristics, with particular emphasis on including underserved groups such as people living with multimorbidity, socioeconomic disadvantage, cultural or language barriers, or other factors that may affect engagement with rehabilitation.
Trial design
Other
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Behavioural determinants influencing adherence to progressive tendon-loading exercise in Achilles tendinopathy
Description: Identification of barriers and facilitators to engagement with NHS-prescribed progressive tendon-loading exercise, derived from semi-structured interview data and mapped to domains of the Theoretical Domains Framework. Time Frame: Assessed at a single time point during interview (reflecting participants' experiences within the previous 24 months).
Secondary outcomes
Prioritised behavioural domains for intervention development
Description: Key domains within the Theoretical Domains Framework identified as most influential and modifiable in supporting adherence, based on thematic analysis and research team consensus (including patient and public input). Time Frame: Derived following completion of data collection and analysis.
Sponsors and contacts
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East Lancashire Hospitals NHS Trust
Lead sponsor
University of East Anglia
Collaborator
University of Leicester
Collaborator
This trial is not recruiting at the moment. You can still explore other options: