STICK2IT - Understanding Why People Do or Do Not Stick With Exercise Treatment for Achilles Tendinopathy

April 21, 2026 updated by: East Lancashire Hospitals NHS Trust

STICK2IT: Identifying and Prioritising Determinants of Adherence to Progressive Tendon-Loading Exercise in People With Achilles Tendinopathy

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.

Study Overview

Detailed Description

Achilles tendinopathy (AT) is a common musculoskeletal condition characterised by pain, stiffness and impaired function of the Achilles tendon. Although progressive tendon-loading exercise is recommended as first-line treatment and has demonstrated efficacy in controlled research settings, outcomes in routine clinical practice are often slower, incomplete and variable. A key explanation for this discrepancy is that the effectiveness of loading-based rehabilitation depends on sustained engagement over time. In real-world NHS care, where treatment is largely delivered through supported self-management with limited supervision, patient adherence to prescribed exercise programmes becomes the primary mechanism through which treatment benefit is realised.

Adherence to rehabilitation is a complex behaviour influenced by interacting psychological, social and environmental factors. Existing research in Achilles tendinopathy has identified a range of commonly reported challenges, including fear of causing harm, uncertainty about exercising in the presence of pain, low confidence in performing or progressing exercises, competing life demands, and fluctuating motivation. These determinants are likely to be further shaped by contextual factors such as multimorbidity, socioeconomic constraints, cultural influences and health literacy. Despite this, current evidence remains largely descriptive and lacks a systematic, theory-informed structure that explains how these factors influence behaviour or how they might be targeted in intervention development.

This study addresses this gap by applying a behavioural science approach to understanding adherence. Specifically, it uses the Theoretical Domains Framework (TDF), an integrative framework that synthesises constructs from multiple behaviour change theories into a comprehensive set of domains. The TDF provides a structured method for identifying the underlying mechanisms that influence behaviour and is widely used in implementation and intervention development research. In this study, the framework will be used to organise behavioural determinants influencing engagement with progressive tendon-loading exercise and to support identification of modifiable targets for intervention.

A qualitative design using semi-structured interviews has been selected to enable in-depth exploration of participants' lived experiences of rehabilitation. This approach allows for the capture of nuanced accounts of how individuals interpret their symptoms, respond to exercise-related pain, integrate rehabilitation into daily life, and interact with healthcare services. It is particularly suited to investigating complex behaviours such as adherence, where individual context and meaning play a central role.

Data will be analysed using an abductive thematic analysis approach, combining inductive and deductive processes. Initially, an inductive analysis will identify patterns of meaning within the data, generating themes that reflect barriers and facilitators to adherence as described by participants. This stage ensures that findings remain grounded in lived experience rather than being constrained by pre-existing theory. Subsequently, these themes will be mapped onto the domains of the TDF to provide a structured, theory-informed interpretation of the behavioural determinants identified.

The use of an abductive approach enables both discovery and explanation: it allows new insights to emerge from the data while also situating those insights within an established theoretical framework. This is particularly important for translating qualitative findings into actionable intervention components. By linking identified determinants to theoretical domains, the study will support identification of potential mechanisms of action that can be targeted through behaviour change strategies.

Following mapping, determinants will be prioritised based on their perceived importance, frequency, and relevance to behaviour change. This prioritisation process will involve interpretive discussion within the research team, incorporating clinical expertise, methodological input, and perspectives from patient and public contributors. The aim is to identify a subset of key domains that represent meaningful and potentially modifiable influences on adherence in the context of NHS physiotherapy.

The study places particular emphasis on understanding adherence within the context of underserved populations. Behavioural determinants are not experienced uniformly across populations, and factors such as socioeconomic deprivation, multimorbidity, cultural context, and access to resources may shape both the nature and impact of barriers to engagement. By ensuring that these perspectives are represented and considered in analysis, the study aims to produce findings that are relevant to real-world service delivery and that support more equitable approaches to rehabilitation.

The outputs of this study will provide a structured, theory-informed understanding of the behavioural determinants that influence adherence to progressive tendon-loading exercise in Achilles tendinopathy. This will form the foundation for subsequent intervention development work, in which identified determinants will be translated into targeted strategies to support engagement with rehabilitation. These strategies may include educational, behavioural, and service-level components designed to address identified barriers and enhance facilitators within routine care pathways.

Importantly, the study is designed as an early-stage component within a broader programme of research. Its primary function is to generate the behavioural evidence required to inform intervention design, consistent with guidance for developing complex interventions. As such, it does not seek to test effectiveness but rather to establish what needs to change, for whom, and through which mechanisms, in order to improve adherence.

In the longer term, improving adherence to evidence-based rehabilitation has the potential to enhance patient outcomes, reduce persistence of symptoms, and improve efficiency within musculoskeletal services. By grounding intervention development in both behavioural theory and lived experience, the study aims to contribute to the design of more effective, acceptable and equitable approaches to supporting patients with Achilles tendinopathy in routine NHS practice.

Study Type

Observational

Enrollment (Estimated)

30

Contacts and Locations

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

Study Contact

Study Contact Backup

Study Locations

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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study 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.

Description

Inclusion Criteria:

  • • 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.

Exclusion Criteria:

  • • 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
    • Unable or unwilling to be audio-recorded.

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
Adults with Achilles Tendinopathy undertaking NHS exercise rehabilitation
This cohort includes adults with lived experience of Achilles tendinopathy who have previously received and attempted to follow a progressive tendon-loading exercise programme prescribed within NHS musculoskeletal physiotherapy services. The intervention of interest is progressive tendon-loading exercise (e.g., eccentric or heavy-slow resistance programmes), delivered as part of routine care and primarily undertaken through supported self-management. Participants will take part in semi-structured interviews exploring their experiences of engaging with and adhering to prescribed exercise, including perceived barriers and facilitators influencing adherence in real-world settings. Particular emphasis is placed on including individuals from underserved populations to capture a diverse range of experiences.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Behavioural determinants influencing adherence to progressive tendon-loading exercise in Achilles tendinopathy
Time Frame: 12 months

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).

12 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Prioritised behavioural domains for intervention development
Time Frame: 12 months

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.

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 (Estimated)

May 1, 2026

Primary Completion (Estimated)

September 1, 2026

Study Completion (Estimated)

May 1, 2027

Study Registration Dates

First Submitted

April 21, 2026

First Submitted That Met QC Criteria

April 21, 2026

First Posted (Actual)

April 29, 2026

Study Record Updates

Last Update Posted (Actual)

April 29, 2026

Last Update Submitted That Met QC Criteria

April 21, 2026

Last Verified

April 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Individual participant data will not be shared for external reuse. Due to the qualitative nature of the study, even de-identified data may carry a risk of participant identification. Pseudonymised data may be shared with authorised research collaborators (e.g., University of East Anglia and University of Leicester) for the purposes of analysis. All data will be stored securely by East Lancashire Hospitals NHS Trust and findings will be reported in aggregate form.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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.

Clinical Trials on Musculoskeletal Diseases or Conditions

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