1. Introduction
Clinical screening tests play a significant role in the rapid assessment of individuals in the day-to-day clinical practice of manual therapists. Although clinical tests are routinely taught and evaluated in physical therapy, the development and validation of standardized assessment methodologies is still far from complete. The prone hip (leg) extension test (PHET) has been widely used for decades as a self-perturbation task to evaluate the stability and function of the lumbopelvic region, as well as to simulate the muscle recruitment pattern of hip extension during gait [
1,
2,
3]. It has been considered a test with good reliability for detecting deviations of the lumbar spine [
4], showing substantial inter-rater agreement [
5], and high specificity, albeit poor sensitivity [
6].
Janda suggested that imbalances between phasic and tonic skeletal muscles may result in a “functional pathology of the motor system,” associated with changes in movement patterns and motor regulation [
1]. These alterations can be observed through the performance of functional tests [
2]. Such muscular imbalances can lead to dysfunctions of the musculoskeletal system and are also associated with changes in both the musculoskeletal and nervous systems, a perspective also supported by Sahrmann [
3]. Although research has mainly focused on the sequence of muscle recruitment patterns—with no clear consensus to date [
4,
7,
8,
9,
10]—rather than on kinematics, some authors have reported kinematic differences. For example, Arab et al. [
11], observed differences in lumbar lordosis angle between patients with and without low back pain. Moreover, the clinical usefulness of the test has been proposed to extend beyond muscle recruitment patterns or kinematics alone: patients perceived “difficulty” in performing the task has been suggested as a clinical indicator of dysfunctional neuromuscular control in individuals with low back pain [
6].
The PHET, as originally described by Janda et al. [
2], has been modified over time with variations in initial and final joint positions. Initial positions have ranged from the classical neutral position [
2,
6,
7,
10,
11,
12,
13], to 30° of hip flexion returning to neutral [
4,
14]. End positions have also varied from neutral [
4], to fixed distances such as 15.4 cm [
9,
10], and 20 cm above the table [
6], as well as to each individual’s maximum hip extension range of motion (ROM) [
13], sometimes with added knee flexion to control lumbar lordosis [
11].
The evolution of the PHET protocol reflects attempts by researchers and clinicians to obtain more detailed information from the test and to adapt it to different clinical settings. To compare the influence of active and passive elements on movement kinematics—which can affect not only joint flexibility but also force production—we administered the test both actively and passively through the full hip extension ROM of each participant, while minimizing trunk compensation. Therefore, the purpose of this study was to examine the differences between active and passive PHET and to investigate how the initial and final hip positions in active and passive conditions correlate with the neuromuscular function of the lower limb.
3. Results
For this study, a sample composed of 7 healthy college students of both genders (2 females and 5 males) was selected. All subjects expressed right lower limb dominance. Anthropometric characteristics regarding age, height and weight are expressed in
Table 1.
The comparison between right and left limbs, whether performed actively or passively, showed no statistically significant differences between dominant and non-dominant limbs actively, with increased abduction and internal rotation in the active test, in the initial positions for right and left legs for adduction/abduction and internal/external rotation for both the initial and final position on the right and for the final on the left leg as shown in
Table 2.
When comparing the difference between the tests performed actively or passively, significant statistical differences were observed only in the FP for rotational movements in both left and right hips and for IP on the right. Significant differences were also observed for the IP in the adduction/abduction movements of the right and left hips. The initial position of the right and left hip in both active and passive tests was in abduction. The FP for the right hip in the active test was external rotation while the FP for the passive test was internal rotation.
Isokinetic variables were correlated with initial and final hip positions in order to understand if initial and final hip positions in the parasagittal plane could influence lower limb neuromuscular functional parameters at different isokinetic speeds (
Table 3,
Table 4,
Table 5 and
Table 6).
The analysis of leg flexion parameters at 180°/s towards flexion showed a significant correlation with the right hip final position in the passive PHET for all parameters except for time to peak torque (
Table 3). Correlations were negative for all parameters except for deceleration, which was positive. All correlations were very strong except for peak torque/body weight which was moderate.
The final position extension ROM was greater in the passive test than in the active form of the PHET (
Table 2).
When we look at the data for extension at 180°/s, all isokinetic parameters showed significant correlations with right hip final position in the passive PHET (
Table 4). Peak torque/body weight, acceleration and agonist/antagonist ratio showed a moderate negative correlation of ρ = −0.75 while time to peak torque and deceleration time showed a positive very strong correlation of, respectively, ρ = 0.81 and 0.90.
Data for higher speeds, which have a higher representation in the real-world activities, at 300°/s towards flexion, only show significant correlations with passive FP of the right hip PHET with the acceleration and deceleration times. Negative for acceleration ρ = −0.82 and positive for deceleration ρ = 0.90 (
Table 5). Initial position for time to peak torque also showed a moderate negative correlation of ρ = −0.75.
The results for 300°/s towards extension (
Table 6) show significant correlations for all the parameters, except for peak torque/body weight extension, with the FP in extension of the right passive PHET. These correlations are positive and very strong for time to peak torque and deceleration time, with ρ values of 1 and 0.95, respectively. Negative significant moderate correlations are observed for acceleration (−0.75) and agonist/antagonist ratio (ρ = −0.79). Regarding IP, significant strong correlations are observed with IP for passive PHET on the left hip deceleration time (−0.84).
When hip position in the frontal plane (adduction/abduction) is analysed at 180°/s towards flexion, only the right hip FP passive is significantly positive correlated with deceleration time towards flexion with a ρ = 0.82 (
Table 7).
Additional correlations were observed when hip position in the frontal plane (adduction/abduction) was analysed (
Table 8). Correlations are found, similar to hip position in the para-sagittal plane, for the dominant right leg in the active test for the IP and FP for time to peak torque (ρ = 0.81,
p = 0.03/ρ = 0.78,
p =0.04), deceleration time for extension (ρ = 0.90,
p = 0.01/ρ = 0.90;
p = 0.01), as well for the passive test, FP peak torque (ρ = 0.81,
p = 0.03) and IP as well as FP, for deceleration time for extension (ρ = 0.77,
p = 0.04/ρ = 0.88;
p = 0.01). The left hip active FP also showed a negative correlation for deceleration time for extension (ρ = −0.76,
p = 0.05).
The same analyses of hip position in the frontal plane at 300°/s towards flexion (
Table 9) showed a negative correlation in the active IP of the left hip (ρ = −0.81,
p = 0.03) and in the passive IP of the right hip for deceleration time for flexion (ρ = 0.81,
p = 0.03).
When hip position in the frontal plane at 300°/s towards extension is analysed (
Table 10), only the passive test showed any correlation of isokinetic variables with hip position in the frontal plane in the IP and FP for time to peak torque for flexion (ρ = 0.86,
p = 0.01/ρ = 0.79,
p = 0.04), for the right hip and deceleration time flex for the left hip (ρ = −0.83,
p = 0.02).
4. Discussion
The objective of this research was twofold: first, to examine the differences between active and passive PHET; and second, to determine how the initial and final hip positions in both active and passive tests correlate with lower limb neuromuscular function.
Functionally, these correlations suggest that passive hip alignment reflects underlying neuromechanical constraints such as passive tension, eccentric control capacity, and torque-production timing. Because passive PHET removes voluntary motor strategies, it may more accurately represent the structural and mechanical characteristics that influence isokinetic performance.
Manual therapists routinely evaluate their patients by assessing changes in movement. Correlating these observed changes with physical performance measures (PPMs)—often referred to in the literature as functional tests—enables clinicians to identify or predict specific functional characteristics following injury, estimate fall risk, and assess sports performance or injury potential [
29].
Regarding the first objective, no differences were observed between the right and left hips in either the active or passive PHET. Consequently, laterality did not appear to influence the initial position (IP) or final position (FP) in the test. The literature has at times been inconsistent regarding laterality, as several studies have reported asymmetries in various skills, strength profiles, and sport-specific adaptations across different athletic populations [
30,
31,
32,
33]. A systematic review by McGrath et al. [
34], reported pooled symmetry ranging from 94.6% to 99.6% across tests, well above the commonly accepted clinical benchmark of 90%, though the sample was biased toward one gender and consisted of asymptomatic individuals. Similar findings were reported by De Lang et al. [
35], in soccer players. When significant imbalances are present, they tend to be associated with pathology in areas such as the groin [
36], patella [
37], and low back [
38,
39]. The results of the present study are therefore consistent with the literature, given that the sample comprised young, asymptomatic college students with minimal sports participation, unlikely to exhibit notable asymmetries or injuries as described by Velotta, Weyer, and Bahamonde [
40].
When comparing active and passive tests across all rotational axes, significant differences were observed only in the frontal plane hip initial position for both right and left limbs, suggesting that lower limb positioning differs depending on whether the movement is performed actively by the participant or passively by the therapist. The same was noted for external rotation of the right limb. In some instances, values were higher (e.g., right passive abduction), while in others they were lower (e.g., left passive abduction and internal rotation on the left versus external rotation performed actively), indicating considerable variability that correlated with only a few neuromuscular parameters. Regarding the final position, only rotational position showed significant differences, particularly when the test was administered by the therapist, seemingly correcting the excessive external rotation observed during active performance. The PHET has demonstrated good reliability in detecting lumbar spine deviation from the midline [
5], and produces lumbopelvic rotation during active limb movement [
41].
These findings may explain the excess external rotation during active testing, in contrast to the internal rotation observed during passive testing, where motor control effects are mitigated by therapist correction.
Few studies in the literature have explored the PHET in terms of movement execution. Most have focused on motor control and low back pain, and to our knowledge, none have examined the relationship between initial and final hip positions and isokinetic neuromuscular variables.
To investigate the potential influence of the rectus femoris and hamstrings—both multiarticular muscles—on lower limb motion and function, knee isokinetic parameters were correlated with hip IP and FP in the sagittal and frontal planes at intermediate (180°/s) and higher (300°/s) isokinetic speeds. Impaired quadriceps function following aerobic exercise has been observed in individuals with recurrent low back pain and healthy knee joints, likely due to a central mechanism arising from poor strength and endurance in spinal musculature [
42]. This may result in repetitive lumbopelvic rotation during active limb movements, a factor implicated in low back pain [
41], and potentially contributing to the frontal plane differences observed here.
Data revealed that at 180°/s, for both extension and flexion, nearly all variables on the right (dominant) side FP showed positive correlations, with the exception of time to peak torque during flexion. Correlations were positive for all variables except acceleration time and agonist-to-antagonist ratio (for both flexion and extension) and peak torque normalized to body weight during extension. At 300°/s during flexion, only acceleration time (negative) and deceleration time (positive) showed significant correlations, whereas during extension, all variables in the passive right PHET were correlated except peak torque normalized to body weight.
Despite the emphasis typically placed on motor control [
5,
13,
43]—where the hamstrings, particularly biceps femoris, have been documented to activate before gluteus maximus in 83% of subjects [
8], consistent with findings from other authors [
10,
43]—our data primarily showed correlations between isokinetic variables and the passive PHET in the right dominant limb. This suggests an important role for passive insufficiency in determining the final position of the PHET, regardless of movement speed.
In the frontal plane, deceleration time was the parameter most consistently associated with significant correlations. At 180°/s during flexion in the passive test of the right limb, and during extension with both IP and FP of the hip (active and passive), significant correlations were observed, as well as with FP in the active test of the left limb. Active and passive hip position in the frontal plane also correlated significantly with time to peak torque, including the IP of the active test at 180°/s. This may partially explain the frontal plane findings, particularly the correlation between FP of the hip and the active right (dominant) limb when compared with isokinetic variables associated with neuromuscular control of agonist-antagonist muscle groups, such as time to peak torque during extension and deceleration time, where significant changes were evident in both IP and FP.
At 300°/s during flexion in the frontal plane, results were less consistent, with the only correlations observed being peak torque normalized to body weight with the IP of the active test on the left, and deceleration time with the passive test on the right. At the same speed during extension, the passive test showed significant correlations with both IP and FP on the right, as well as between FP in the passive test on the left and deceleration time. At higher speeds, the isokinetic component of movement is reduced, which may account for the decreased number of neuromuscular variables correlated with hip IP and FP during the PHET.
Limitations
The PHET is assumed to reflect the muscle recruitment pattern of the hip during functional tasks such as the mid-to-late stance phase of walking and running. The hypothesis that it may influence neuromuscular function of the knee is plausible but requires further investigation. The sample size in this study was limited, and future research should include larger, more diverse samples encompassing both sexes and varying limb dominance profiles. Pelvic rotation should be assessed during initial evaluation to determine whether it influences initial and final PHET positions and whether it correlates with isokinetic neuromuscular function.