Life expectancy in people with hemophilia has increased since the 1950s due to advances in management and improvements in factor replacement therapy.1 There is now concern that, as more people with hemophilia reach older age, there will be an increase in age-related disorders such as overweight, obesity, cardiovascular disease, and cancer. Research suggests that the prevalence of age-related disorders among people with hemophilia is probably at least comparable with that of the general population,2-4 though not uniformly so.5, 6
The UK government strategy to address cardiovascular risk factors such as inactivity, overweight, and obesity is to be “physically active including at least 150 minutes of moderate intensity activity each week, in bouts of 10 minutes or more, or 75 min of vigorous activity across a week or a mixture of moderate and vigorous activity.”7 Guidelines for the management of hemophilia recommend tailored physical activity focusing on bone health, muscle strengthening, coordination, physical functioning, healthy body weight, and positive self-esteem.8
There is no published evidence on the prevalence of sport participation or physical activity in people with hemophilia in the United Kingdom. In the UK subpopulation of the HERO study (n = 52 people with hemophilia and 50 parents of children with hemophilia), 23% and 12% of adults, respectively, reported swimming or cycling; the figures for children were 70% and 48%.9 In the SO-FIT study using HaemoQoL, 127 boys (aged 8-17) with well-controlled hemophilia self-reported good physical functioning but impairment in the domain “sports and school.”10 In one UK study (n = 50; 64% obese), 64% of adults with hemophilia reported sports participation, and those who did not attributed this to their physical condition (but not obesity) or fear of injury; quality-of-life scores were higher in those who participated in sports.11
These studies suggest that people with hemophilia engage in physical activities and, in this respect, may not differ from the general population, but a large proportion face challenges to participation because of hemophilia. To explore these issues further, a small exploratory qualitative study was conducted in young men with hemophilia (n = 10), several of whom reported a sport-related injury.12 This showed varying levels of motivation to engage in physical activity and differing levels of confidence due to perceived injury risk. It was also highlighted that physiotherapy often did not address a desire to be able to do nonrehabilitation exercise activity such as gym-based weightlifting and higher-level muscle strengthening.
To date, almost all of the published literature concerning exercise in hemophilia relates to hospital-based rehabilitation,13 postsurgical rehabilitation,14, 15 or physiotherapy-led home exercise programs for specific outcomes such as balance.16 Recent reports show no additional injury or bleeding risk from sporting activity in young people with hemophilia,17 but to our knowledge no literature exists that describes nonmedicalized exercise approaches for people with hemophilia such as gym-based weight training. Younger people with hemophilia want to have the option of using gyms for their own self-identified health and fitness goals, but still identify barriers related to their hemophilia.
Personal trainers (PTs) are an increasingly common sight in gyms. They work on an individual basis with people to design strength and physical fitness programs based on identified goals and physical ability. The personalized nature of this kind of training may provide psychological reinforcement around motivation and goal attainment18 and has been shown to positively change attitudes toward exercise and increase physical activity.19 While PTs are professionally trained in health and fitness across a spectrum of physical conditions, their knowledge of rare diseases such as hemophilia would be minimal.
This study was conceived to investigate the feasibility of a PT-led fitness program on motivation and adherence to exercise for young adults with hemophilia. The aims of this study were twofold: Investigate the feasibility, safety, and acceptability of a randomized, PT-led fitness program for young men with hemophilia. Collect and analyze preliminary data (amount of change before and after) with the chosen outcome measures relating to motivation, adherence, self-efficacy, and physical activity. 2 METHODS 2.1 Study designThis was a multicenter, nonblinded, randomized feasibility study.
2.2 ParticipantsPotential participants were identified from registration databases at three large hemophilia centers by physiotherapists. Inclusion criteria specified people with haemophilia A or B of any severity, aged between 18 and 25 years living within 90 minutes’ travel time of the gym location and with good command of written and spoken English. If the local medical team deemed participation in this study as unsafe, participants were not included (Table 1).
TABLE 1. Study inclusion/exclusion criteria Participant inclusion criteria Participant exclusion criteriaAged 18-25 years
Diagnosis of hemophilia A or B – any severity
Able to give informed consent
Lives within 90 min travel to the gym study site
Able to understand and read/write English
Adults for whom the study was deemed unsuitable by their medical team
Limited comprehension of English (needed for safe participation)
Travel time >90 min to gym study site
2.3 Recruitment/enrollmentThe recruitment period was for 6 months, from January to June 2018. Potential participants were mailed an information sheet and invited to contact the investigators by phone or email if they wanted to participate. Those who did not respond within 2 weeks were followed up by telephone to check if they had received the study information and if they wished to participate. Final participants were invited to a study workshop held at the gym. Written consent was taken at this point.
2.4 InterventionThe gym location was the YMCA in Central London. Before the study commenced, the gym manager was contacted and agreed to inform all the PTs working there about the project. PTs who expressed an interest in taking part were invited to a study information, education, and training session delivered by the study team in advance of the participant workshop (Table 2). On the day of study commencement, participants were invited to attend a workshop hosted in the gym facilities. Here, they participated in the delivery of a brief education curriculum (Table 2), and a tour of the gym facilities was provided by the PTs. Baseline demographic data was collected by physiotherapists and PTs; health information was provided by each of the participants (Table 3).
TABLE 2. Education curriculum for study participants and personal trainers Project GYM – Curriculum Young men with hemophilia Personal trainers Hemophilia and its effect on joints How to train safely in gym/personal limits How to use equipment safely and effectively Principles of nutrition How to recognize/manage bleeds versus normal physical response to exercise (such as muscle soreness) When to seek professional help Core program of gym-based fitness activities Introduction to fitness opportunities available within gym Basics of hemophilia Psychological and sociological aspects of living with hemophilia The effect of hemophilia on and in a family Rationale for this study Overview of physiotherapy assessments Risk modification Management and outcome assessments Self-activation and behavioral change skills TABLE 3. Participant characteristics at baseline All (n = 19) PT group (n = 9) Gym group (n = 10) Age, y Median 22.1 22.07 21.08 Range 18.1-24.1 19.06-24.06 18.09-24.10 Type of hemophilia A/B 14/5 7/2 7/3 Severity of hemophilia Mild 4 0 4 Moderate 3 2 1 Severe 12 7 5 Treatment Standard half-life factor 15 6 9 Extended half-life factor 3 3 0 Desmopressin 1 0 1 Dose of factor 1500-3500 IU 2000-3500 IU 1500-3000 IU Injection frequency Weekly 1 1 0 Alternate days 6 3 3 On demand 6 1 5 Othera 6 2 4 BMI, kg/m2 Median (range) 23.4 (17.3-39.9) 23.5 (17.6-39.8) 22.3 (17.3-30.9) Body fat mass, % Median (range) 20.6 (4.3-43.3) 14.8 (4.3-43.3) 23.4 (18.8-38.2) Smoker 4 2 2 Hemophilia Joint Health Score (total) Median 0 0 1 Range 0-13 0-13 0-13 Self-reported bleeds in past 6 monthsb Median 1 1.5 1 Range 0-6 0-6 0-3 Comorbidityc Number of participants 4 3 1 Visited family physician in past 4 weeks 2 2 0 Ethnic background White 12 6 6 Black/Black British 1 0 1 Asian 4 1 3 Other 1 0 1 a Daily (1), 2-3 times/week (1), every 3 days (2), weekly (1), twice monthly (1). b Two participants were unable to provide an exact figure; two did not provide data. c May have reported more than one comorbidity: glucose intolerance/diabetes (1), depression/anxiety (2), overweight/obesity (2), lower back pain (2), osteoarthritis (1), musculoskeletal (1), other (1). 2.5 RandomizationRandomization (“gym only” or “gym and PT”) was completed using a sealed envelope system after consent, curriculum delivery, and questionnaire completion.
Those randomized to the PT arm were offered a 12-week tailored, PT-led fitness program. They met the PTs after randomization and were able to choose the PT with whom they wanted to train. In keeping with a real-world approach to using the service of a PT, the participants arranged their own follow-up sessions with their PT. At their first session, they agreed on goals for their program, and the PT designed a bespoke exercise program for them based on this. This enabled a highly individualized and personal program for them, based on their own identified physical needs, interests, and identified goals. As a result, no two participants did the same program. The PTs were also encouraged to contact the specialist hemophilia physiotherapist known to each participant if they felt they needed further advice or guidance. Hemophilia center physiotherapists, however, did not participate in the development of any exercise plans. Participants were allowed one face-to-face session per week for 12 weeks with their PT. They could choose to independently attend the gym as many times as they wished in addition to this. Those assigned to the gym-only arm were provided with a gym induction session and encouraged to do self-directed gym activity for 12 weeks. Both groups were advised to follow their programs for a further 12 weeks (24 weeks in total).
Participants on prophylaxis adjusted their treatment regimen, in agreement with their medical team, to allow factor administration before gym activity. All participants had free gym membership for the duration of the study, with an optional extension at study completion at a reduced price for a further 6 months.
2.6 MeasurementsThe Hemophilia Joint Health Scores (HJHS) for each participant were requested from the physiotherapist at their hemophilia center. Those with mild or moderate hemophilia without a recent HJHS were invited by the physiotherapist to attend this review before starting the study.
Participants completed baseline study questionnaires (Table 4) that focused on assessment of readiness to change (the Stages of Change questionnaire),20, 21 degree of self-efficacy for management of their chronic disease (the Self-Efficacy to Manage Chronic Disease Scale [SEMCD]),22 generic health-related quality of life (EQ-5D),23 type and intensity of physical activity in daily life (the International Physical Activity Questionnaire [IPAQ]),24 and a measure of self-esteem (Rosenberg’s Self-Esteem Scale).25
TABLE 4. Questionnaires used in the study Stages of change Assesses readiness to change behaviour through a series of characteristic stages (precontemplation, contemplation, preparation, action, maintenance, and relapse) toward adopting and maintaining a new habit. Self-Efficacy to Manage Chronic Disease Scale Assesses self-efficacy for managing chronic disease using six items on a visual analogue scale (VAS; 0–10). Higher scores indicate higher self-efficacy. International Physical Activity Questionnaire (IPAQ) – short form Assesses the types and intensity of physical activity and sitting time that people do in their daily lives. The IPAQ short form has seven questions to self-report physical activity in the preceding seven days. The score is calculated by multiplying the time and level of activity; higher scores indicate greater activity. Rosenberg’s Self-Esteem Scale Consists of five positively and five negatively worded statements, that individuals score using a 4-point scale, from strongly agree to strongly disagree. Scores range from 0 to 30; scores below 15 suggest low self-esteem. EQ-5D-5L Standardized generic instrument that comprises five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression, which together can be used to calculate a respondent’s health status. A visual analog scale (where 0 is worst and 100 is best health status) is also included. Higher scores represent higher health.All participants were issued a Fitbit Versa 2 activity tracker and instructed on how to connect to the “Fitabase” data collection system and how to upload their activity data. The consent form included permission for the study team to access activity data (step count and heart rate) for the duration of the study. To minimize any potentials bias, participants were only informed they could keep the Fitbit after they completed all the study procedures and had been assigned to their randomized group.
At 6 months, participants were invited to a follow-up workshop, completing the same questionnaires as at baseline. Follow-up HJHS assessments were also requested. All participants were contacted for an interview with one of the study team, either face to face or over the phone, to discuss their experience of the study and whether they had maintained any changes in activity. A telephone call was made at 12 months to ascertain if any gym activity continued.
2.7 Feasibility outcomes These were identified as: Recruitment rate (how many were eligible and ability to recruit planned number [n = 20] in time period) and follow-up rate (how many were successfully followed up at 6 and 12 months). Acceptability of study procedures, chosen outcome measures, and randomization (assessed through post-study interviews). Safety of intervention (assessed by number of recorded bleeds, for any reason) and any other adverse events (such as injury). 2.8 Statistical methodsData are presented as descriptive, with median and range data, and interquartile range where appropriate. Statistical analysis was done using SPSS (version 25;IBM, Armonk, NY, USA). Interviews were recorded and transcribed verbatim; transcripts were coded and analyzed thematically.
2.9 Sample sizeBecause this was designed as a feasibility study, there was no need to achieve a desired power to detect any effect. The study aimed to see if this could be done in the way it was conceived and delivered.
The study was approved by the Ethics Committee and Health Research Authority in accordance with local governance and legal requirements (IRAS project ID: 241384; REC reference 18/WA/0179). The study was registered with the Research and Development Office of the Royal Free Hospital, London, UK.
3 RESULTS 3.1 Demographic dataParticipant demographic data are presented in Table 3. Nineteen participants were recruited, with a median age of 22.1 (18.1-24.1) years. Fourteen had a diagnosis of hemophilia A, 12 had severe hemophilia, 3 were moderate, and 4 were mild. Participants were from diverse racial backgrounds, with median body mass index and adiposity (23.4 [17.3-39.9] and 20.6 [4.3-43.3], respectively). Joint health was good: 13 participants had HJHS scores of between 0 and 3, two scored 7 and 8, and three participants had scores of 12 and 13.
3.2 Recruitment and retentionParticipant identification, recruitment, and retention for the study are detailed in Figure 1. Nineteen participants were recruited, compared to the original aim of 20. HJHS data were unavailable for 15 participants (78.9%) at 6-month follow-up. Outcome measure data were not available for two participants (10.5%) at 6 months, as they did not attend the follow-up workshop or return questionnaires by post. Only 10 participants (52.6%) agreed to an interview at 6 months, five over the telephone and five face to face. At 12 months, only seven (36.8%) agreed to a follow-up phone call.
Recruitment and retention of participants in study. HJHS, Hemophilia Joint Health Score
3.3 Attendance ratesParticipants who were randomized to the 12-week PT-led fitness program visited the gym more frequently (median visits, 16; range, 3-83) than those with gym membership only (median visits, 3; range, 3-41).
3.4 Activity levelsPhysical activity levels (reported via IPAQ) showed that in the PT group, activity level increased in five participants, with no change in five. In the non-PT group, there was an increase in activity level for four participants, with no change for three.
At 12 months, seven participants reported that they were still attending a gym, with two individuals continuing to pay for a PT.
3.5 FitbitFitbit activity data were available for 17 of 19 participants at 6-month follow-up. Participants did not synchronize their data regularly with the Fitabase system; therefore, quality of the overall data was poor. Across the group, median total steps per day was 7937 (range, 4287-17 182). Data on heart rate were consistently poor, with multiple missing data points, so we are unable to include it here.
3.6 Joint health in studyThe HJHS remained unchanged at 6-month follow up for 63.2% of participants (n = 12), with a decreased total score in 15.8% (n = 3; range, 1-3 points improvement). It did not increase in any participant. There were no follow-up HJHS data available for four participants.
3.7 Adverse eventsAt baseline, participants were asked to estimate how many bleeds (all bleeds) they recalled having in the preceding 6-month period. A total of 78.9% (n = 15) reported bleeds (range, 1-3), with 21.1% (n = 4) reporting zero bleeds.
Self-reported bleed data were available for only 17 participants (84.2%) at the 6-month follow up. Of these, 68.8% (n = 11; seven participants in the PT group and four in the gym-only group) reported bleeding episodes (median, 2; range, 1-5), with 37.5% reporting no bleeds (n = 6; three in the PT group and three in the gym-only group). The follow-up interviews revealed that none of the reported bleeds were gym related (one shoulder injury, one low back pain, one “ankle problem,” one wrist injury, and one trauma related to a wall-climbing injury).26 Comparing bleeding rate before and after the intervention, 37.5% (n = 6) reported fewer bleeds (range, 1-5), 37.5% (n = 6) reported an increase in bleed rate (range, 1-4), and 25% (n = 4) reported no change. Of those reporting an increase in bleed rate, one had moderate hemophilia; of those reporting decreased or no change in bleed rate, five had severe hemophilia, one had moderate hemophilia, and four had mild hemophilia. None reported this increase as being associated with being part of the study.
3.8 Outcome measuresResults are shown in Table 5.
TABLE 5. Global changes in efficacy end points Measure Statistic PT group Gym-only groupPrestudy
[n = 10]
Post-study (6 months)
[n = 10]
Prestudy
[n = 9]
Post-study (6 months)
[n = 7]
Stages of change Change in grouping (start vs end)Precontemplation (0)
Contemplation (1)
Preparation (3)
Action (3)
Maintenance (3)
Precontemplation (0)
Contemplation (0)
Preparation (0)
Action (1)
Maintenance (9)
Precontemplation (0)
Contemplation (0)
Preparation (1)
Action (0)
Maintenance (8)
Precontemplation (0)
Contemplation (0)
Preparation (0)
Action (0)
Maintenance (7)
International Physical Activity Questionnaire (IPAQ) Change in score (start vs end)Low (2)
Moderate (3)
High (5)
Low (0)
Moderate (2)
High (8)
Low (2)
Moderate (4)
High (3)
Low (0)
Moderate (2)
High (5)
Self-efficacy Change in score (start vs end)Median = 41
Range = 19-60
Median = 54
Range = 25-60
Median = 53
Range = 25-60
Median = 49.5
Range = 43-60
EQ-5D index score Change in score (start vs end)Median = 0.74
Range = 0.41-1.00
Median = 0.82
Range = 0.51-1.00
Median = 0.84
Range = 0.69-1.00
Median = 0.79
Range = 0.62-1.00
EQ-5D VAS Change in score (start vs end)Median = 72.5
Range = 15-97
Median = 80
Range = 45-98
Median = 75
Range = 40-100
Median = 80
Range = 55-96
Self-esteem Change in score (start vs end) Total score Median = 23 Range = 12-30Median = 24
Range = 13-30
Total score Median = 22
Range = 14-28
Median = 26
Range = 18-30
In the PT group, the median change in the SEMCD from baseline to study end (six months) was 41 (range 19–60) and 54 (range 25–60), compared to the non-PT group which was 53 at baseline (range 25–60) and 49.5 (range 43–60) at study end.
For the EQ-5D-5L index score, the PT group had a median change from baseline to post-study of 0.74 to 0.82 compared with a slight decrease of 0.84 to 0.79 for the non-PT group.
Self-esteem score in the PT group had a median change from baseline to post-study of 23 (range, 12-30) to 24 (range, 13-30), with a slightly larger change found in the non-PT group of 22 at baseline (range 14-28) and 26 (range, 18-30) at study end.
3.9 AcceptabilityAt the 6-month follow-up, only 10 participants (52.6%) agreed to be interviewed about their views and opinions on their experience of the study, and as such only a limited evaluation is possible here. Participants reported that the measures chosen were acceptable in terms of time to complete and assessment type. Activity monitoring via Fitbit was acceptable, even though there was low adherence to uploading data. Reasons for poor adherence to wearing/using the Fitbit included losing it and remembering to charge it. One preferred a different device as it was part of his health insurance plan. All reported they were happy to be randomly assigned and understood its purpose. One participant randomly assigned to PT failed to contact the PT, stating that he was “happy just to have access to the gym to do his own thing.” Fifty percent of this group (n = 5) were happy with the gym location. Reasons given by participants for the gym location being problematic included living too far away to travel and trying to get there after work.
4 DISCUSSIONAlthough exercise is broadly recommended for people with hemophilia, private gym-based exercise activity has yet to be fully investigated. To our knowledge, this is the first time such an approach has been attempted. As such, response and adherence to self-structured exercise (as opposed to hospital-based rehabilitation or prescribed home exercises) remains unknown. This feasibility study demonstrates that self-directed and PT-supported gym activity is safe, that joint health (HJHS) was not negatively affected, and that PT-led activity encourages increased participation.
Health equity for people with hemophilia is intrinsically associated with access to prophylaxis – allowing normal mobility and participation in work, school, and family life without restriction.27 This normalization of lifestyle also normalizes the risk of trauma associated with an active lifestyle. This applies to the cohort in this study whereby the overall benefit of being physically active outweighs risk of inactivity associated with hemophilia.
Recent reviews of exercise for people with hemophilia have been broadly encouraging with regard to its safety as an intervention. Poor-quality studies and lack of reporting of methods and findings mean that care must still be taken with such recommendations.28, 29 However, as shown in our findings, safety in participation with gym-based exercise programs was demonstrated. It is noteworthy that none of the studies included in these two reviews used private gym facilities – they were either home exercise programs or physiotherapy rehabilitation facilities. It remains that exercise in people with hemophilia is heavily medicalized even when not associated with an acute clinical episode. In contrast, recent findings from a Dutch cohort suggest that nonmedicalized sports participation appears to be a safe activity in young people with good joint health receiving adequate prophylaxis.17
Being physically active as a child predicts increased participation in physical activity in adulthood,30 with activity that has been supported by parents, peers, and teachers enhancing self-awareness and confidence in activity as an adult.31 For many adults with hemophilia, normal parti
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