Participants
The participants were a total of 30 physical therapy students (male: 18, female: 12, age: 19.6 ± 0.83 years), including 22 second-year students and eight third-year students at the four-year university in Kumamoto Prefecture, Japan. Participants were asked for their cooperation after verbally explaining the content of this study and how to handle the results in advance while showing them the research manual. Consent was obtained by signing the consent form themselves. This study was approved by the Ethics Committee of the Kumamoto Health Science University (approval number: 22007). By the time they participated in the study, they had completed lectures and exercises on joint range of motion measurements; however, they had never performed ROM measurements on patients during training at a hospital.
Measuring equipment
The participants used a universal goniometer with a handle length of 30 cm and angle marks at 1° increments. In this study, the reference ROM values for the knee joint were measured using ARMS software (ATR-promotions, Kyoto, Japan) based on the measured values obtained by two electronic accelerometers (TSND151, AMWS020; ATR-promotions, Kyoto, Japan). The values measured by the accelerometer were transferred to a computer connected via Bluetooth, and the joint angles were calculated based on these values and displayed on a screen in real time. Previous studies have confirmed the reliability of knee joint angle measurements using electronic accelerometers for various movements such as walking, climbing stairs, and jumping. In particular, high reliability has been reported for measurements in the sagittal plane [46]. For left knee flexion measurements, an accelerometer was attached to the lower limb 5 cm from the lateral epicondyle of the femur along the line connecting the greater trochanter and lateral epicondyle of the femur, whereas the other accelerometer was attached 5 cm from the fibular head along the line connecting the fibular head and lateral malleolus. These landmarks were identified by palpation. In addition, electronic accelerometers were installed using the method described by Yamamoto et al. [45]. All accelerometers were secured with surgical tape, whereas elastic bandages were used to prevent slippage. The joint angles calculated from the accelerometer measurements and saved at a sampling frequency of 1,000 Hz were displayed on a monitor using ARMS software to notify individuals who underwent ROM measurements of the joint angles.
Tasks
Goniometric measurement task
In this study, with reference to the study by Akizuki et al., the task was to measure the ROM of the left knee joint of the subject in the supine position [35]. The landmarks for the ROM measurement of the knee joint were the greater trochanter, lateral epicondyle of the femur, fibular head, and lateral malleolus. The angle formed by the line connecting the greater trochanter and lateral epicondyle of the femur and the line connecting the fibular head and lateral malleolus was measured in 1°steps by the participant using a universal goniometer (Figure 1). No instructions were provided on how to locate the landmarks by palpation, passively bend the joint, or apply a goniometer to the measurement site. During the trials, the right knee joint flexion was set to angles of 60° ± 10°, 75° ± 10°, and 90° ± 10°. The person to be measured watched the display of the software, and when the set angle was reached, announced that “the knee will not bend any further” and resisted the force being applied to flex the knee by the participant. Once the movement stopped, participants measured the joint angle in 1° increments using a universal goniometer. Furthermore, as soon as they completed the measurements, they declared “done” and reported the measurements to the experimenter. The experimenter recorded the time at which the measurement was completed using the time-recording function of the ARMS software. The person to be measured was the same for all participants.
Visual estimation task
The visual estimation task was performed in the same manner as the goniometric measurement task, with only the method of measuring the joint angles being changed. In this task, the subject passively flexed the subject's left knee joint, and when it stopped, observed it directly and estimated the joint angle in 1° increments without using a device such as a universal goniometer.
Procedure
The participants were randomly divided into two groups: a self-control group (SC group) and a Yoked group (Yk group). The number of students in each group was the same. All participants participated in the two-day experiment according to their assigned groups (Figure 2). First, SE before the pretest was measured before practice. Each item was scored on a ten-point Likert scale, with 1 indicating a lack of confidence and 10 indicating complete confidence. Many studies on SE have used the Likert scale, although the scores are not uniform and range from 5 to 10 points [47, 48]. According to Gist et al., with high baseline SE, room for improving SE is low [49]. Therefore, to increase the possibility of score dispersion, we used a ten-point Likert scale, which was also used in the fall efficacy scale [50]. After measuring SE, three trials [60° ± 5°, 75° ± 5°, and 90° ± 5°; in random order) of both the visual estimation and goniometric measurement tasks were conducted as a pretest. The acquisition phase was conducted after the pretest. In the acquisition phase, 12 trials (3 trials × 4 blocks) were conducted, and the three joint angles were randomly set for three trials in each block. During practice, after the visual estimation task, the participants performed the goniometric measurement task while keeping their left knee joint. There was a 30-second break between each trial and a one-minute break between each block.
During practice, participants in the SC group chose whether to receive feedback at the end of each trial and were given feedback on the goniometric measurement task only during the preferred trials. The feedback information was the joint angle displayed on the screen when the subject declared completion of the measurement and the experimenter verbally communicated it to the subject in 1° increments. In contrast, the participants in the Yk group were not given the opportunity to make a choice and received feedback only on trials in which the corresponding participants in the SC group received feedback. In addition, the participants in the Yk group performed the tasks in the same order as the corresponding participants in the SC group.
After completing the practice, SE was measured again, followed by a short-term retention test in the same manner as in the pretest. Approximately 24 h after the end of the short-term retention test, SE was measured, and subsequently, the long-term retention test was conducted in the same manner as the pretest. Furthermore, the participants were not provided feedback on either test.
Figure 2 represents the schematic diagram of the measurement procedure. SE of the ROM was measured before each test. In all the tests, the goniometric measurement and visual estimation tasks were measured in the same manner, with three trials each. In the acquisition phase, the participants practiced each task for a total of 12 trials (3 trials × 4 blocks). In addition, feedback was provided according to the condition of the assigned group only during practice, and no feedback was given to all participants during all tests.
Data processing and statistical analysis
First, because the feedback frequency for the SC group fluctuated with the participants’ choices, the feedback frequency was calculated for each block. Next, we set measurement accuracy and measurement time as indicators of ROM measurement technique. The measurement accuracy indicates the accuracy of the technique, whereas the measurement time indicates the smoothness of the technique. The main results of this study were the measurement accuracy and measurement time of the goniometric measurement and visual estimation tasks in each test and the SE for ROM measurement before each test. First, the accuracy of the goniometric measurement task was calculated as the absolute error between the joint angle measured by an electronic accelerometer and that measured by the student using a universal goniometer. Similar to the goniometric measurement task, the measurement accuracy of the visual estimation task was defined as the absolute error between the joint angle measured using the electronic accelerometer and the student's visual estimation. Next, for both the goniometric measurement and visual estimation tasks, the measurement time was defined as the time from the experimenter's declaration of the start of measurement to the participant’s declaration of the completion of measurement and was measured in milliseconds. These results were averaged for each task in the pretest, short-term retention test, and long-term retention test. SE was defined as the real number on a ten-point Likert scale as the SE of the ROM measurement before each test measurement.
Statistical analysis was performed using IBM SPSS ver.29 (IBM Corp., NY, USA). To verify the changes in feedback frequency, we conducted a one-way analysis of variance with the feedback frequency of each practice block as the dependent variable and the practice block as the independent variable. If a significant main effect was found, a Bonferroni test was performed. Subsequently, an analysis was conducted to determine the degree of learning for each task based on the differences in the accuracy of goniometric measurements and visual estimation and the difference in the way feedback was provided. A three-way analysis of variance was conducted with measurement accuracy as the dependent variable and testing, feedback, and measurement method (3 × 2 × 2) as factors. A sub-test using the Bonferroni method was performed if a significant main effect or interaction was observed. A similar analysis was conducted regarding the measurement time of the goniometric measurement method and visual estimation. Finally, to confirm whether the SE of each group was related to the measurement accuracy of the goniometric measurement task, the measurement accuracy of the goniometric measurement task of each test and the SE before each test were subjected to Spearman correlation analysis. A similar analysis was performed on the measurement accuracy of the visual estimation task. In all analyses, a risk rate of less than 5 % was considered statistically significant.