3.2. Participants
This study utilized a cross-sectional observational research design. The participants were 70 individuals with FHP disorder, aged between 17 - 45. They were selected from physiotherapy centers in Ahvaz city and from among the employees and students of Ahvaz University of Medical Sciences who had FHP (IR.AJUMS.REC.1400.707). These individuals were divided into mild and moderate-to-severe groups based on their craniovertebral angle (CVA). The two groups were similar in terms of variables such as age, sex, height, weight, and body mass index. The method and manner of conducting the test were fully explained to the participants, and they were asked to sign an informed consent form approved by the Ethics Committee of Ahvaz Jundishapur University of Medical Sciences. Then they entered the study.
The inclusion criteria for the study were: Age between 17 - 45 years, suffering from FHP, and no history of neck pain or neck injury in the past 6 months. Individuals who had a history of fracture or surgery in the neck area (
18,
24), vision problems not corrected with glasses (
25), neurological and neuromuscular disorders, inflammatory diseases, rheumatoid arthritis, congenital anomalies (
26), moderate and severe scoliosis, severe thoracic kyphosis or breathing problems (
1,
17,
24), headache or dizziness, vestibular system disorders (
25,
27), lower limb injuries (
1,
17), acute, intermittent, or radiating neck pain (
25,
27), or drug or alcohol use in the previous 24 hours (
27) were excluded from the study.
3.3. Procedure
First, the subjects were asked to stand in a comfortable position with their weight evenly distributed on both feet, looking straight ahead next to a rope hanging from the ceiling and passing in front of their lateral malleolus. Then, based on Kendall's definition, participants who had an ear tragus forward from the shoulder or trunk were diagnosed with FHP (
28). In previous studies, the high reliability of Kendall's diagnostic method has been confirmed with a Kappa coefficient of 0.73 (
1,
29).
Afterward, to determine the severity of FHP, a camera (Canon G10, Japan) was placed on a tripod at a distance of 1.5 meters from the individual at the same height as their shoulders, and the participants were photographed in a side view (
30). Before taking the picture, the tragus points of the ear and the location of the spinous process of the seventh vertebra (C7) were identified and marked using markers. To identify the spinous process of the C7, the participants were asked to flex and extend their heads several times in a full range while standing, and then the spinous process of the C7 was identified (
5).
After that, the CVA was measured by calculating the angle between the horizontal line that passes through the C7 and the line that connects the point of the tragus of the ear to the C7, using Kinovea software (
Figure 1) (
1,
6,
24,
27). A CVA of 45.5 degrees was considered the cut-off point for categorizing mild and moderate-to-severe degrees. People with a CVA less than 45.5 degrees were placed in the moderate-to-severe group, and those with a CVA greater than 45.5 degrees were allocated to the mild group (
10). According to Mostafaee et al.’s study, CVA has good accuracy (AUC = 0.88) in discriminating between individuals with mild and moderate-to-severe FHP. Additionally, this angle has a sensitivity of 0.93 and a specificity of 0.62, making it valuable for correctly identifying mild FHP and screening moderate and severe grades of FHP (
31).
The limits of stability test was performed using a posturography device (NeuroCom, Equitest, USA). The posturography device consists of three main parts: The force plate, the screen, and the main computer body (
4). This test evaluated the individuals' ability to voluntarily move their center of gravity and to assess stability in a dynamic state. Subjects were asked to stand on a force plate in front of a screen set at eye level and to voluntarily move their center of gravity toward fixed target points from different directions as far as possible without stepping or losing their balance (
20). During this test, the force plate remained constant. On the screen, there was a central square target, with eight other squares in primary and secondary directions (front, back, right, left, front-right, front-left, back-right, back-left). These eight squares represented the person's limits of stability in each direction, determined by the computer at 45° intervals around the center of gravity based on the person's height (
21).
Before the main test began, the subject was familiarized with the test and instructed that the position of the human-like character on the screen would move according to their movements and weighting. This character represented the person's center of gravity, which had to be kept in the central square at the beginning of the test. At the start of the test, while keeping their hands at their sides with palms facing the thighs, the participants stood on the specified place on the force plate. After hearing a beep, they moved their weight toward the target with maximum possible speed and accuracy. They maintained the same posture until the target sign disappeared and they heard a second beep, which lasted for 8 seconds. The person's weight transfer during the test focused on the movement of the ankle joint, and they were instructed not to change the position of their legs or bend backward during the test (
Figure 2).
A, The NeuroCom limits of stability test (LOS). The center target is the starting point; B, A participant wearing a safety harness and standing on the dual force plate support surface, looking at the visual surround.
Finally, the device averaged the person's performance using EquiTest software in terms of five indicators: Movement reaction time (RCT), movement velocity (MVL), endpoint excursion (EPE), maximum excursion (MXE), and directional control (DCL) in eight directions: Forward (FW), backward (BW), right (RT), left (LT), forward right (FWRT), forward left (FWLT), backward right (BWRT), and backward left (BWLT) (
20,
21). The definitions of these variables are given below:
- Reaction time is defined as the time between the movement announcement signal and the start of the person's movement, measured in seconds.
- Movement velocity is the average movement speed of a person in degrees per second, calculated during 5-95% of movement (distance from the starting point). To calculate the speed more accurately, the computer removes the first and last 5% where acceleration is increasing and decreasing.
- Directional control is a comparison of the amount of movement in the desired direction (toward the target) to the amount of movement outside the range (away from the target), expressed as a percentage.
- Endpoint excursion is the distance traveled by the person's center of gravity on the first attempt to transfer weight to the target, expressed as a percentage of the person's limit of stability, indicating the person's tendency to move within their limit of stability.
- Maximum excursion is the farthest distance traveled by the center of gravity in each repetition, expressed as a percentage.
3.4. Statistical Analysis
SPSS version 26 was used for statistical analysis. A confidence interval of 95% and a significance level of P < 0.05 were considered for all analyses. To check for the normal distribution of data, the Kolmogorov-Smirnov (K-S) test was used. The results showed that the distribution of data was normal. Therefore, the t-test was used to determine the statistically significant difference between the two groups of individuals with mild and moderate-to-severe FHP in terms of the average values of age, height, weight, and body mass index. Furthermore, for each LOS variable, we performed a separate 2 × 5 mixed model analysis of variance (ANOVA). The between-group factor was group (mild FHP, moderate-to-severe FHP), and the within-group factors were direction of the LOS (Forward, Backward, Right, Left, and Overall). If there was a significant interaction of group-by-direction of the LOS variables, a comparison between groups was performed using independent-sample t-tests.