Hypermobility spectrum disorders (HSDs) and the hypermobile subtype of Ehlers-Danlos syndrome (hEDS) are conditions that predominantly affect females [1]. While the true prevalence of these conditions is unclear and thought to be underestimated [2], the combined prevalence of HSD/hEDS has been reported to be 1 in 500 (Wales, United Kingdom), and recent unpublished data have shown a prevalence of 1 in 227 (Northumberland, United Kingdom) [1,3]. HSD/hEDS may be characterized by recurrent joint injuries, chronic pain, generalized fatigue, and muscular weakness [4]. As a result, many individuals with HSD/hEDS report a fear of new or reinjury due to movement (kinesiophobia), and many tend to be physically inactive [5-7]. Inactivity may further exacerbate HSD/hEDS symptoms [6,7], prompting a vicious cycle of symptoms reinforcing sedentary behavior and vice versa.

Physical activity (PA) is defined as any movement that increases energy expenditure above resting levels [8,9]. PA may be categorized as structured (exercise, sports, and occupational activities) or unstructured (play, household, or leisure activities, and functional daily movements such as walking or climbing stairs) [9]. Exercise is a structured form of PA that is repetitive, structured, and purposeful for improving health or fitness [9]. PA has known health benefits, including improved cardiovascular, bone, and mental health [8]. As the physical and cognitive benefits of PA may improve quality of life in HSD/hEDS [5], a better understanding of optimal guidance and prescription of PA for this population is needed, particularly around the salient risks and tangible benefits of PA.

Females with HSD/hEDS have reported worsening symptoms and more frequent joint injuries during puberty, pregnancy, and at various points in their menstrual cycles [10]. Symptom severity and injury frequency have also been reported to improve after menopause [10]. Changes in symptoms and injury risk during these times may impact an individual’s ability to participate in PA. To our knowledge, there has been no mention of female sex hormones, puberty, the menstrual cycle, pregnancy, or menopause in previous reviews of structured exercise in HSD/hEDS [11-17].

The World Health Organization International Classification of Functioning, Disability, and Health (ICF) is an internationally recognized classification system that provides a conceptual framework to determine outcomes relevant to daily function, including physical, cognitive, social, and environmental domains [18]. An ICF model has been developed specifically for Ehlers-Danlos syndromes based on clinical presentations and patient experiences, revealing that HSD/hEDS impacts each domain of the ICF [5,7]. Therefore, the ICF provides a relevant framework to categorize PA-associated outcomes related to quality of life for individuals with HSD/hEDS.

Guidance as to what PAs are safe, appropriate, and beneficial for living with HSD/hEDS may help reduce pain and fear associated with PAs in this population. Prior reviews have focused on exercise interventions as part of physical therapy treatment in HSD/hEDS, including therapeutic exercise and strength training alongside manual therapy or other modalities for rehabilitation [11-17,19]. However, multiple knowledge gaps remain. Prior reviews did not consider children, older adults, effects of female sex hormones, or times of female hormonal changes during the lifespan, unstructured PA, or any structured activities outside of physical therapy and rehabilitation, such as different sports or occupational activities. Therefore, this scoping review will help identify what PAs are appropriate and safe for individuals with HSD/hEDS outside of a physical therapy session, if PA should be adapted during specific times of female hormonal changes, and how PA across the lifespan may be affected. This will help guide clinicians in PA counseling for symptom management and improved quality of life in this patient population [5].

This protocol will detail the methodology of the proposed scoping review, which will appraise the evidence regarding the safety and impacts of structured and unstructured PA for individuals of all ages with HSD/hEDS. Categorizing the effects of PA in HSD/hEDS based on ICF domains will provide a comprehensive description of the impacts on quality of life. As female sex hormones may influence symptoms of HSD/hEDS, it is also important to consider hormonal changes across the lifespan when assessing the safety and impacts of PA. Based on the state of the literature, a scoping review is justified [20].

The aims and research questions are listed in Textbox 1.

This proposed scoping review will follow the methodology described by Arksey and O’Malley [20], Peters et al [21], and the PRISMA-ScR (Preferred Reporting Items for Systematic Reviews and Meta-Analyses extension for Scoping Reviews) [22]. Any deviations from this protocol will be included as an update within the OSF (Open Science Framework) registration and a supplementary document in the final review. Ethics approval from an institutional review board was not necessary, as this review will only pursue secondary use of publicly available published data.

Eligibility criteria will be defined according to the PCC (population, concept, and context) format [22] (Table 1).

Databases to be searched include MEDLINE, Embase, CINAHL, SPORT Discus, and Scopus with a search end date of September 5, 2025. Study designs such as randomized controlled trials, nonrandomized controlled trials, prospective and retrospective cohort studies, case-control studies, cross-sectional studies, qualitative studies (phenomenology, ethnography, qualitative descriptions, etc), and case studies will be included. Systematic reviews and meta-analyses that meet eligibility criteria will be excluded but flagged for citation chaining. Study designs that will be excluded from this review include conference abstracts or proceedings, editorials, commentaries, and gray literature. Citation chaining will be used for the studies included in the data extraction phase.

The search strategy was developed in consultation with DWG, CAJ, and RHKM and performed by a health sciences librarian with experience developing search strategies and performing searches for systematic reviews (LD). A preliminary search was conducted in Ovid MEDLINE to refine the keywords and terms used in the search strategy. This involved running the search with the selected MeSH (Medical Subject Headings) terms and text words in MEDLINE and reviewing the results in consultation with all coauthors. We then performed a preliminary screening of 100 papers to further refine the search terms and keywords. The search strategy will include subject headings (MeSH) and text words related to HSD/hEDS and PA such as Ehlers-Danlos, hypermobility, exercise, gymnastics, stretching, dancing, fitness, PA, sports, tai chi, yoga, qigong, running, swimming, walking, activity tracker, step count, pedometer, daily activities, active lifestyle, housework, manual labor, gardening, and yard work. As the tertiary aim is exploratory, there is no need to add additional keywords related to female hormones, as any relevant papers will be identified using the above strategy. The search will be limited to English, and no date limit will be applied. The search strategy will be adjusted for the specific formatting of each database, and results will be uploaded to the Covidence web-based software platform.

Covidence software will be used to manage the reviews. Three reviewers will independently perform title and abstract screening and full-text review. Reviewer training will involve an educational session outlining the aims, inclusion and exclusion criteria, and screening procedures for each step of the review. Reviewers will be asked to read a reference instructional manual specific to these procedures. Following this, title-abstract calibration will be performed using the first 100 abstracts. Reviewers will independently review the abstracts, and then conflicts and questions will be discussed during a formal debriefing session to ensure consistency between reviewers and consensus in understanding the eligibility criteria. If needed, the instructional manual will be updated. Full-text calibration will be similarly performed through reviewing the first 2 manuscripts assigned to reviewers B and C with reviewer A, who will be reviewing all manuscripts (Figure 1). Again, if needed, the instructional manual will be updated. The screening protocol is shown in Figure 1.

Studies must meet eligibility criteria based on the agreement of 2 reviewers at the title and abstract screening stage, as well as at the full-text review stage, to be included for data extraction. For any studies where 2 reviewers are uncertain after screening the title and abstract (maybe-maybe), these studies will be included for full text review for further assessment against the eligibility criteria. Disagreements between 2 reviewers (yes-no, yes-maybe, or maybe-no) at any stage will be resolved by discussion between all reviewers. Journal titles and original study authors will not be blinded. Interrater agreement for screening and full text review will be reported as Kappa scores.

Data extraction will follow the ICF framework. Data items and outcomes according to ICF domains are listed in Table 2. A data extraction template will be created using this framework. Outcomes will be grouped based on the keywords for data items in Table 2. Data extraction will be performed independently by 5 reviewers. Reviewers onboarded for data extraction (D and E) will be trained as described in the screening protocol. Included research studies will be assigned to each of the 4 reviewers (B, C, D, and E), with the fifth reviewer (A) extracting every study to ensure consistency and extraction by the 2 reviewers per paper (Figure 1). Any discrepancies between reviewers will be resolved by consensus discussion between the 5 reviewers. Similar to screening and review, full-text calibration will be performed through extracting the first 2 research studies assigned to each of the 4 reviewers (B, C, D, and E) with the fifth reviewer (A), who will be extracting all included studies. If needed, the instructional manual will be updated. Operational definitions and methods of measurement for each outcome will be extracted and summarized in a table in the final review. Data management will include secure storage of search strategies, the review protocol, reviewer notes, and extracted data in an online Microsoft OneDrive (Microsoft Corp) shared between all authors. The data extraction sheet will be reported as a Multimedia Appendix in the final scoping review. Authors of the original studies will be contacted if information related to the population, concepts, or outcomes is unclear. Three email attempts will be made (once every 2 wk) to the corresponding author to obtain missing information. If no response is received, the missing data will be reported as “not reported” and will not be included in the data synthesis.

Two patient and 4 clinical knowledge users have been involved in the design of this review and the multifaceted integrated knowledge translation plan through formal quarterly meetings. The lived experiences of these knowledge users informed the research questions and specific aims of this review. Specifically, the influence of hormonal contraceptive use on the safety and impacts of PA was included in the research aims based on feedback from these knowledge users. Based on feedback from the knowledge users, the findings of this review will be shared with individuals living with HSD/hEDS, clinicians, and researchers. We will present this at an annual event for patients, researchers, and clinicians and expect attendance to exceed our 2024 event, which was attended by 106 individuals in person and 117 online. We will share the results through a webinar with copresentation with the knowledge users. The knowledge users will also help us craft plain-language summaries of the research findings to be shared on the laboratory websites of the authors. Our research team will generate infographics summarizing the published review to share on social media to reach patients and caregivers. Based on the principal investigator’s laboratory social media metrics, we would expect approximately 300 people to access the infographics. The findings will also be shared with clinicians through 2 local education sessions (1 for physicians and 1 for physical therapists) and 1 provincial education session for physical therapists. Clinicians and researchers will be targeted through presentation at 1 international conference, the publication of this protocol, and the final review.

Findings will be summarized in separate tables related to each research aim. In accordance with the guidelines for scoping reviews [28], quality assessment of methodology and risk of bias will not be performed. Analyses will include frequency counts and descriptive statistics, including percentages or proportions. A narrative summary will be performed to articulate the current state of knowledge regarding the safety, benefits, and harms of PA in HSD/hEDS and patient-specific considerations. This approach has been recommended when including both qualitative and quantitative research designs [29].