1. Introduction
After knee surgery, the treating clinician and other health care professionals (HCPs) are in charge of evaluating the individual course of a patient. Ensuring sufficient and adequate remobilization following surgery requires the clinician to accurately monitor the patient’s mobility and physical activity. However, it is difficult for HCPs to observe the mobility a patient has reached in daily life if they have to rely on patients’ self-reports. Such reports may be unreliable due to social desirability or cognitive impairments [
1]. Physical activity trackers (PATs), based on accelerometers and other sensors, are promising to provide objective information concerning patient mobility [
2], and validated user-friendly tools are commercially available [
3,
4]. Consequently, HCPs have, today, the opportunity to use PATs within their clinical routine, as well as for purposes other than monitoring. There already exist 39 systematic reviews on the intervention effects of PATs [
5] and 15 studies on using commercially available PATs after total knee arthroplasty [
6].
However, it is often unclear whether a specific PAT is indeed suitable for monitoring the changing level of mobility in a surgically treated patient. Early remobilization after surgery—in particular, after surgery of the lower extremities—may be characterized by slow, low-impact, and sporadic movements. In contrast, PATs have often been validated using healthy adults. Thus, they may simply fail to recognize low-level mobility. Indeed, a systematic review found that a specific tracker showed decreased validity when applied in unhealthy populations or at slow walking speeds [
7]. There is an ongoing debate about the validity of PATs during early recovery [
8,
9,
10,
11,
12,
13,
14]. Two studies have explicitly investigated the validity of different step counters at a walking speed of 0.4 m/s, and came to contradictory conclusions [
15,
16]. The use of walking aids seems to be an additional challenge for PATs [
17,
18,
19]. Consequently, it is hard for HCPs to judge the information provided by a specific step count if there is some suspicion that not all steps are counted. Understanding the detection limits of a PAT helps to interpret step counts correctly. This also applies to information provided by a PAT beyond step counts, e.g., activity profiles based on a classification of physical activities, as most physical activities are achieved through short bouts of low-intensity activity.
A further issue arises from the continuous updating of a PAT’s algorithm by the manufacturer in order to improve the measurement process [
20]. Hence, also for validated PATs, there is always some risk that their measurement properties have changed [
21,
22]—especially for unusual user groups, such as patients after surgery. Thus, a quick ad hoc validation is desirable.
It would be useful to have a simple protocol that can be used by HCPs to familiarize themselves with the detection limits for low-impact-steps of a specific PAT. Preferably, such a protocol should also take into account some additional conditions under which patients typically perform physical activities during the recovery phase. For example, many activities are performed indoor at home within a potentially cluttered environment or walking aids may be used. The protocol should be feasible for any HCP. In particular, it should be possible for HCPs to carry out the protocol without the need for additional equipment.
The aim of the current study is to propose and test such a protocol for the specific case of patients after knee surgery. The basic idea is to ask HCPs to wear the PAT, to perform steps similar to those they expect in patients during recovery after knee surgery, to vary the impact and other characteristics of the steps, and to always compare the number of steps they performed with the count shown by the PAT (cf.
Figure 1). The basic approach to testing the protocol is to invite HCPs to carry out the protocol. This allows us to study its feasibility and whether HCPs can identify differences in detection limits across different conditions. In addition, the HCPs were asked to complete the protocol twice in order to study reproducibility.
2. Materials and Methods
2.1. The Protocol
The protocol consists of a series of conditions. Under each condition, the HCP performs twenty steps while wearing the PAT and aiming to mimic the gait of patients at varying stages after knee surgery. After each condition, the HCP inspects the number of steps counted by the PAT, which allows the HCP to make a comparison with the true number of steps.
The conditions are based on combinations of the following factors (Italic font indicates the abbreviations later used to refer to factor levels):
| 1 | Step size intended: | 25%, 40%, 75%, 100% of normal step size. |
| 2 | Direction: | Straight line, turn by 90° after 10 steps; zigzag line, 90° |
| | | shifts after 5, 10, and 15 steps; 360° circle clockwise. |
| 3 | Use of walking aids: | Without walking aids; with walking aids |
| 4 | Footwear: | Street shoes vs. home slippers. |
The following 14 combinations are considered in specific order: S-100, S-75, S-40, S-25, T-75, Z-75, C-75, T-40, Z-40, C-40, W-75, W-40, L-75, and L-40.
In order to allow HCPs to get an idea of the intended changes in step size, a video illustrating the conditions S-100, S-75, S-40, and S-25 is provided (publicly available at
https://osf.io/yrz7c (accessed on 29 October 2025)). It is recommended that HCPs watch this video and familiarize themselves to the conditions by performing some practice trials prior to executing the protocol. In addition, it is recommended that HCPs wear a bandage on one knee to remind them to perform the gait in a somewhat asymmetric manner.
2.2. Elaboration of the Protocol
Walking speed is well known to influence a number of gait-related variables, and its impact on a PAT’s ability to detect steps has been previously demonstrated [
7]. Consequently, the first factor is aimed at controlling walking speed. As it is hard to directly standardize the speed of steps without external equipment, we decided to phrase the differences with respect to step size. Furthermore, low-impact steps typical for patients after knee surgery are not only characterized by reduced step sizes, but also by other aspects, such as reduced motor control, which manifest as clumsiness and heightened cautiousness. Consequently, we produced a video explaining the intended differences in speed and reminding users of the protocol to mimic the gait of patients after knee surgery.
In contrast to laboratory-based gait studies, in which steady walking on a straight line is usually examined, patients after knee surgery may perform the majority of their physical activities at home with obvious spatial restrictions. Hence, 20 steps taken in a straight line are unlikely to represent a typical behavior. Consequently, as the second factor, we consider a variety of deviations from a straight-line gait, which differ in the frequency and abruptness of the directional changes. These variants may have an additional impact on the detection properties of PATs to that of walking speed alone. Finally, two additional aspects are taken into account that are related to the recovery process—the use of walking aids—or to the home environment of the patients—the use of slippers. These constitute the third and fourth factors, respectively.
As a full factorial design covering all 64 possible combinations does not seem to be feasible, an incomplete factorial design is suggested. Regarding the combination of a straightforward direction at a step size of 75% or 40% with no walking aids and street shoes as the two core conditions, these two conditions are systematically varied with respect to one of the four factors, resulting in 14 conditions.
With respect to the sequence of the conditions, we suggest starting with S-100, reflecting “normal” gait in a patient, and to reduce the step size sequentially such that the HCP becomes more familiar with the step sizes also used later. We then focus on the three variants in walking direction at step size 75%, followed by the same three variants at 40% step size. We prefer to vary the direction in the first place, as we regard this as conceptually simpler than a change in step size. The placement of the four final conditions reflects the need to use specific equipment.
We do not specify the use of a specific walking aid. This way the HCP can choose the walking aid preferred in her or his patient population or which is at hand for the HCP. The four step sizes are not equidistantly chosen in order to have a sufficient difference in step size when considering only two step sizes while varying factors 2 to 4.
2.3. Study Population and Recruitment
Aiming at a protocol suitable for all HCPs in contact with patients after knee surgery, we included three different groups of HCPs, varying in the type of contact: orthopedic surgeons, physiotherapists, and sport scientists. All HCPs were required to have experience with managing patients after knee surgery.
Members of the project team—located at a multi-disciplinary clinic specialized in orthopedics and sport medicine—approached colleagues by email and invited them for participation. Interested HCPs were provided written study information and signed informed consents at the study visit. The study visits took place between 12 March and 26 June 2024.
2.4. PATs Used
HCPs were required to simultaneously wear four different PATs during the protocol. The four PATs selected are described in
Supplemental File S1, together with the criteria for their selection. They comprise a sensor integrated within a shoe
sole, a sensor attached to the
knee, a sensor which can be worn in the
trouser pockets, and a sensor to be worn at the
wrist (
Supplemental Figure S1). We refer to them in the following sections by their wearing location. They also involve different technologies to identify steps such as force-sensitive resistors, inertial measurement units, triaxial accelerometers, gyroscopes, magnetometers, temperature sensors, and barometers. Due to the differences in technology and wearing position, we expected differences in the ability to detect steps across the four PATs.
2.5. The Experimental Setup
Participants were invited to a single 90 min visit at the Biomechanics Lab at the crossklinik, Basel, Switzerland. Each participant was asked to wear their “usual” shoes and to bring a pair of slippers. The conduct of the study activities at the Biomechanical Lab was guided by varying instructors supported by varying assistants from the sport science group of the crossklinik. They had been partially involved in the development of the protocol.
The participants obtained detailed instructions and performed a few trial walks to become familiar with the tasks involved, i.e., using different step sizes, changing directions, performing a reading of the step counts from the different devices, using walking aids, etc. This included a 20-step walk in a straight line with a normal step size. From this walking distance, the assistant then calculated the corresponding distance for 25%, 40%, and 75% step size and marked them to support the later evaluation of whether the intended step size was reached. However, the marking was not communicated to the participant. Participants were asked to wear a bandage (Genumedi, E+Motion) on the right knee, while the knee sensor was placed on the left knee. The factor level “Turn” was implemented as a right turn, whereas the factor level “ZigZag” started with a left turn. Forearm crutches were used as a walking aid and the HCPs were asked to use a partial weight-bearing technique, which was also demonstrated by the instructor.
The trouser and the wrist sensors were set in a mode where steps were counted continuously. Before and after performing the steps under each condition, the participant read off the step count from these two sensors and communicated them to the assistant. The assistant computed the difference and communicated it back to the participant. The sole and knee sensors allowed the assistant to directly read off a step count from the accompanying app and to reset the app after each condition. The numbers were directly communicated to the participant. The two step count differences and the two step counts were recorded on a paper case report form (CRF) by the assistant.
The participants were asked to repeat the walk when the instructor identified that the performance of the task varied markedly from the experimental condition. The assistant counted, in any case, the number of steps performed by the participant and also recorded this on the paper CRF.
After performing the steps under all 14 conditions, the whole procedure was repeated in a second round. After the first round, the instructor asked the participants for the following information: age, gender, profession, and years of experience in working with patients after knee surgery. The information was recorded on the paper CRF. The participants were also asked to assess the value of the protocol and of the sensors by answering the following two questions separately for each PAT on a paper form:
Do you now have an idea of the quality of the different sensors under the conditions used? (A precise idea/Some idea/A vague idea/No idea)
Do you feel this PAT is suited to monitor the physical activity of patients after knee surgery? (This PAT is perfect/This PAT is well suited/This PAT is of limited value/This PAT is of no value)
2.6. Analytical Strategy
Although we aim at a fixed number of steps across all conditions, slight variations in the number of steps performed cannot be excluded. Hence most analyses will be based on the step count ratio, i.e., the ratio between the observed step count and true step count in a specific condition. A ratio close to 1 indicates that the PAT can detect a patient’s low-impact steps for this condition.
The inclusion of different conditions in the protocol aims at allowing the HCP to learn about the varying detection limits of the PAT. It is hence desirable to observe some systematic variation in the step count ratios across the conditions for a single PAT. Consequently, the first analytical step is to compare the distribution of the step count ratios—and, in particular, the mean values—across the different conditions. It is also of general interest to understand the influence of the different conditions on step counts, as this may reflect general limitations in assessing the steps of patients after knee surgery.
A good protocol should ensure that different HCPs come to a similar judgment about the same PAT. Hence, the HCPs should experience similar differences in step count ratios across the different conditions. Consequently, one outcome of interest is the inter-HCP reproducibility of step count ratios across the different conditions within the same PAT. As the sufficient intra-HCP reproducibility of step count ratios is a prerequisite for sufficient inter-HCP reproducibility, we first analyze the intra-HCP reproducibility before analyzing the inter-HCP reproducibility.
Potential participant effects on the step counts were assessed by visual inspection of the raw data. Finally, we report the distribution of the responses of the participants to the two questions about the value of the protocol and the value of the sensors.
2.7. Statistical Methods
Raw data: The raw data of the step count ratios were depicted by dot plots stratified by experimental condition and PAT, with the values of the two repetitions connected by a line. Participants were numbered in the order of their study visits.
Effects of conditions: The effect of conditions on the step counts was analyzed by a zero-inflated negative binomial regression model with the number of true steps as exposure and the experimental conditions as the only covariate. This model takes into account that conditions may influence the detection limit—implying, potentially, that no steps can be detected—and the ability to count steps above the limit correctly to a different degree and that participant effects introduce heterogeneity in counts. A potential dependence between different step count ratios within one HCP was taken into account by basing statistical inference on the Huber–White sandwich estimator [
23,
24]. Selected contrasts for marginal means (based on setting the true step count to 20) were considered to assess the effect of the step size within the categories S, T, Z, C, W, and L and the difference between category S and categories T, Z, C, W, and L, respectively. In addition, the
p-value of testing the null hypothesis of no difference between all conditions was reported. A 5% statistical significance level was used.
Reproducibility of step counts—general considerations: Regarding step count ratios as quantitative measures, the reproducibility can be described by the intra-class correlation coefficient (ICC). However, in this study, step count ratios aimed at distinguishing three possible outcome scenarios for a specific experimental condition and a specific PAT:
The PAT is able to identify steps under this condition. In this case, we expect a ratio close to 1.0.
The PAT is unable to identify steps under this condition. In this case, we expect a ratio close to 0.0.
The experimental condition is close to the limit at which the PAT can detect step counts. In this case, we have to expect the step count ratio to be rather unstable and may cover a rather wide range of values.
Consequently, ICCs are limited with respect to catching the reproducibility of interest, as they expect reproducibility over the whole scale from 0.0 to 1.0. To address this issue, we consider also weighted agreement rates. In determining the degree of agreement between two single step count ratios, the following weights were used:
0.0—If one step count ratio is above 0.8 and the other is below 0.2;
0.5—If one step count ratio is between 0.5 and 0.8 and the other is below 0.2, or if one step count ratio is between 0.2 and 0.5 and the other is above 0.8;
1.0 If both step count ratios are between 0.2 and 0.8, or if one step count ratio is above 0.8 and the other above 0.5, or if one step count is below 0.2 and the other is below 0.5.
The choice of the thresholds 0.2 and 0.8 reflects that even true ratios of 0 or 1 might be affected by some noise. The agreement rate of a set of a pair of step count ratios was then defined as the average weight over all pairs. As pointed out in
Supplemental File S2, such agreement rates can also be transformed into
values following the principle introduced by Cohen [
25]. In verbalizing the magnitude of these
values, we applied the classification into poor, slightly, fair, moderate, substantial, and almost perfect using the cut-off values 0.2, 0.4, 0.6, and 0.8 suggested by Landis and Koch [
26].
Reproducibility of step counts: For each participant and PAT, the intra-HCP reproducibility was assessed by a kappa value and an ICC. These were based on all pairs of step count ratios observed for the same condition across the first and second round in one HCP (
Figure 2). For each PAT, the inter-HCP reproducibility was assessed by a kappa value and an ICC. These were determined by computing these values for each pair of HCPs and each combination of rounds using all pairs of step count ratios observed for the same condition and averaging over all HCP pairs and over all combinations of rounds (
Figure 2).
Computation of the ICC was based on a random effect model with the conditions as random effects using the restricted maximum likelihood (REML) technique. The reporting was omitted if the standard deviation of the random effect was less than 0.1. Reporting of kappa values was omitted if all step count ratios were above 0.5.
Statistical software: All computations were performed with Stata 17.1. The code for the main analyses is documented in
Supplemental Files S3 and S4.
Sample size: In the study protocol, two different scenarios varying in the expected agreement rate between two HCPs were simulated and the precision of the estimates of the agreement rate were compared. It was concluded that 16 HCPs would be sufficient to distinguish the two scenarios.
4. Discussion
4.1. Summary of Main Results
The protocol turned out to be feasible for all participating HCPs. For two PATs, the protocol allowed the HCPs to experience differences in the step count ratio across different conditions.
The sole and the knee sensors performed nearly error-free over all conditions, and this result was shared among HCPs. This also resulted in a rather uniform, favorable judgment about the value of these two sensors. Due to technical problems, however, the knee sensor could only be experienced by 5 of the 14 HCPs.
The trouser sensor was the only device that showed clear differences in the average step count ratios across the conditions. Hence, only for this sensor did we reach a favorable precondition to assess the value of the protocol by considering reproducibility for all participants. We observed, on average, a substantial intra-rater reproducibility, suggesting that essential differences between step count ratios can often be reproduced when repeating the protocol. The inter-rater reproducibility was only fair, indicating some limitations of the protocol with respect to ensuring comparable results across HCPs. However, it is notable that all HCPs were in agreement in providing an unfavorable judgment about the value of the sensor.
With respect to the wrist sensor, the moderate degree of systematic differences between the conditions limited the possibility of investigating the reproducibility in a systematic manner. However, a simple visual inspection of the raw data indicated clear participant effects on the step counts: some participants experienced step count ratios close to 1.0 over all conditions in both rounds, whereas other experienced a substantial variation across conditions and rounds. This variation in experiencing variation across the conditions may also explain the mixed opinions about the value of this sensor.
4.2. Implications with Respect to the Value of the Protocol
In general, our study confirmed that the protocol has the potential to inform HCPs about the utility of the PATs in detecting specific types of low-impact steps that can be expected in patients after knee surgery: it allows HCPs to observe corresponding differences in step counts for a PAT across the conditions considered—if they exist.
It was our aim to develop a protocol with a sufficient standardization of the input presented to the PATs, such that HCPs can come to similar conclusions about the detection limits of a PAT and its general value. This was the case for the sole and the knee sensors—which is, however, a highly trivial result as the sensor could detect nearly all steps. We were also, to some degree, successful with respect to the trouser sensor with a substantial intra-observer reproducibility on average and nearly moderate inter-observer variability. However, we failed with respect to the wrist sensor with clear differences between HCPs.
When trying to explain the difference between the trouser and the wrist sensors, the paired design of the study is a key element: the steps produced by the HCPs—and actually any movement of the body—were exactly the same. Hence, from this perspective, the “input” to both PATs was the same. Consequently, the wrist sensor must have been sensitive to some information in the input representing noise (relative to the information on the steps), e.g., to other types of body movements we did not control by our instructions. This would indicate an insufficient step counting quality of the sensor in this specific clinical context and not a failure of our protocol. This is in line with our observation that participants could experience substantial variation in step count ratios although the systematic differences across the conditions were small.
It can also be argued that, from the perspective of a single HCP, the main purpose of varying conditions is to generate some meaningful variation in the HCPs gait and to allow the HCP to experience how his or her choice of gait influences the ability of the PAT to detect steps. This aim is still reached even if the interpretation of the instructions and hence the input to the PATs differs from HCP to HCP. On the other hand, it is additionally desirable that HCPs experience at least roughly the same condition in the same manner. If HCPs differ in their impressions about which type of steps a PAT can detect, they will also differ in the interpretation of an activity profile generated by the PAT, and hence potentially in the consequences in managing a patient.
4.3. Potential Improvement of the Protocol
The limited inter-observer variability calls for some measures to further standardize the input to the PATs generated by the HCPs. The use of auditory or visual cuing to control step size and step frequency may be an option. Such approaches may, however, influence other gait parameters and may distract the HCPs from the task of mimicking the gait pattern of patients. Virtual or augmented reality [
27,
28] or biofeedback [
29] may overcome this drawback. In addition, it might be possible to increase the quality of the input with respect to mimicking patients after knee surgery. Instead of a simple bandage, more specific means may be used, e.g., braces or orthotics, or patients could be used in generating the instructional video.
There still remains a need to identify further conditions which may reflect challenges for a PAT to identify steps correctly and which are likely to occur during the recovery period of patients after knee surgery. This can be, for example, other types of walking aids such as walking frames or supporting persons, performing half steps instead of full steps, walking upstairs or downstairs, or to differentiate between open-heeled footwear and closed footwear. Simulating a complete home environment to study the measuring properties of PATs has been recently suggested [
14].
It might also be of interest to extend the protocol by allowing or forcing the HCPs to repeat conditions. This way, we can diminish the risk of false conclusions due to some unintended random variation in the input. In addition, this way, HCPs can take the condition-specific reproducibility of step counts into account in generating an opinion about the reliability of a PAT.
4.4. General Aspects of the Value of the Protocol
It constitutes a basic limitation of the protocol that it cannot be applied to all conceivable PATs. HCPs are typically interested in monitoring patients over time periods of several days and weeks. This may require the pre-processing of measured data and storing relevant information with low sampling frequency. It might be impossible to read off step counts after 20 steps under such conditions. This is the case, for example, with the Active Insights Band (
https://activinsights.com/technology/activinsights-band (accessed on 29 October 2025)), which was especially developed for HCPs.
An advantage of the protocol is that it can be easily adapted by the HCP to meet specific needs or interests. If an HCP has concerns regarding specific gait patterns, corresponding conditions can be simply added to the protocol. The protocol can also be easily adapted to other patient groups, e.g., patients after hip surgery, abdominal surgery, or poly traumata, by generating corresponding videos and adjustments of conditions.
As with any experimental protocol applied to humans, potential risks have to be balanced against the gain in information. Rapid turns, zigzags, and the use of crutches is not without risk. However, as HCPs constitute the intended user group, it seems fair to expect that users can balance risk vs. information gain individually.
4.5. Further Aspects
Our study confirms that the impact energy of steps can have a substantial influence on the detection of step counts by a PAT. In addition, deviations from moving straight forward, which commonly occur in non-laboratory environments, can influence the performance of a PAT to detect steps. The use of crutches resulted in an average decrease of eight steps counted by the trouser sensor, but no such effects could be observed for the other PATs. This underlines that the effect of walking aids on the detection of steps is device-specific, and the use of crutches may not necessarily constitute a problem.
A nearly optimal overall accuracy indicates that the sole sensor would seem an expedient candidate for further investigation of its usefulness in monitoring the physical activity level of patients. However, the sensor is predicated on the concomitant use of footwear, which may represent a practical limitation to its application in the home environment, where footwear may not be routinely used. A high overall accuracy could also be observed for the knee sensor. Technical problems with the accompanying app do not necessarily reflect an obstacle for its use, as the sensor offers two different modes for short-term and long-term observations.
The inclusion of a popular fitness tracker (the wrist sensor) allowed us to address the potential wish of patients to use their own tracker to monitor post-surgical rehabilitation. For some HCPs, the sensor failed to detect steps under some conditions. This suggests some risk associated with the use of such a tracker, as it may not work well for some patients. This is in line with a reported average relative error rate of more than 40% for step counts from a 100 ft walk in patients after knee surgery when using two popular fitness trackers [
9].
With a few exceptions, the sole sensor consistently underestimated the true number of steps by one step, independent of whether the participant succeeded in 20 steps or not. This probably reflects that there was always a half step at the start and at the end of the 20 steps.
4.6. Limitations of the Study
It was a distinct limitation of this study that only one of the four PATs tested showed clear differences between the different experimental conditions and that two of the sensors worked perfectly for all conditions. This prohibited further analyses planned in the study protocol, in particular, the usefulness of conditions to distinguish between PATs and the similarity of conditions in this respect. This would have allowed us to develop suggestions for removing conditions providing similar information.
The failure to include the slipper condition implies a risk of overlooking a potential challenge to the PATs and the limited amount of data for the knee sensor may have prevented further insights from a high-quality, but still imperfect, sensor.
The limited number of participating HCPs and the distinct association between the four HCP characteristics assessed prohibited an investigation of the latter with respect to a potential influence on step count ratios and inter-rater reproducibility.
It cannot be excluded that the variation in instructors across the participants has contributed to the limited inter-HCP reproducibility. Similarly, the assessment of the ground truth by the assistant need not be error-free, contributing to the underestimation of reproducibility.
The intended sample size of 16 HCPs was not reached. However, the sample size consideration aimed at ensuring that moderate differences between PATs with respect to detection limits could be demonstrated. Fortunately, the differences were rather distinct, and hence 14 HCPs were sufficient to obtain insights.
It can also be seen as a limitation that the participants were asked about their opinion on the value of the protocol and of the sensor only once after the completion of the first round. This choice reflected the wish to catch the intended use in practice, i.e., a single application of the protocol. An additional interrogation prior to executing the protocol would have allowed the assessment of a change in opinion, while an additional interrogation after the second round would have allowed the assessment of the effect of experiencing a repetition.
4.7. Outlook
Our investigation illustrates the feasibility of self-familiarizing health care professionals with the detection limits of a physical activity tracker using specific protocols. At the moment, the proposed protocol has to be used with some care, as it cannot be ensured that all HCPs will come to the same conclusion for all PATs. We recommend trying to reproduce findings when using the protocol in order to judge their reliability. In addition, further research is necessary regarding how individual variations in gait can influence the detection of steps by PATs. This may help us to understand their general usefulness in this patient population and to improve the protocol. Corresponding studies should implement a stricter control of conditions and additional data collection (e.g., video recordings) than the present study, which focused on a proof of principle.
The idea of self-familiarization of HCPs with PATs before offering them to their patients is a rather general one. The use of an experimental protocol to generate the input to PATs is only one possibility. Alternatively, real-world input can be used. For example, to investigate the validity of daily or weekly activity profiles, HCPs may wear the sensors themselves for some days and compare the recorded profile with the activities they actually did.
The lack of concrete protocols to facilitate the clinical application of PATs has been identified as a major barrier to their use to improve patient care [
30]. The development of protocols for self-familiarization can make a contribution to enhance the clinical use of PATs and supplement existing guidelines for the implementation of PATs in clinical practice [
31].