Chronic pain (CP) is one of the most significant global health challenges due to its high prevalence, impact on disability, and economic burden (
1). Notably, a substantial proportion of CP sufferers are women (
2). The recognition of sex and gender disparities in CP prevalence has been well-established, with numerous epidemiological studies highlighting differences across various CP conditions, including back pain, musculoskeletal pain, headaches, and arthritis (
3). Murray et al. (
4) reviewed 43 studies involving 97,437 young adults from 22 countries, finding an overall pooled prevalence of CP in young adults at 11.6%, indicating that approximately 1 in 9 young adults worldwide experience CP.
In recent years, there has been increasing attention to the link between CP and post-traumatic stress disorder (PTSD) (
5). Post-traumatic stress disorder is a common anxiety disorder that can arise after exposure to traumatic events such as accidents, violence, or war (
6). It is characterized by three primary symptom clusters: Hyperarousal, intrusive memories of the traumatic event, and avoidance of situations and stimuli associated with the event (
7). Post-traumatic stress disorder is associated with an increased risk of both psychological and physical health issues, often leading to significant physical, occupational, and social impairment (
8). Pain is frequently reported among the physical symptoms of PTSD, regardless of the type of trauma experienced (
9).
Åkerblom et al. (
10) found that individuals with both CP and PTSD exhibited higher levels of pain severity, pain interference, depression, and cognitive fusion, along with lower levels of pain-related acceptance and committed action compared to those without PTSD. Similarly, Akhtar et al. (
11) reported that 28% of 300 consecutive CP patients screened positive for PTSD, a rate higher than that of the general population. Those who screened positive were typically younger and experienced greater pain intensity than those without PTSD.
The biopsychosocial approach to CP is widely regarded as the most effective framework for understanding and managing CP (
12). According to this model, numerous studies have emphasized the impact of CP on psychosocial factors, including psychological distress (PD), such as anxiety, depression, and stress (
13,
14). The duration of pain and individuals' beliefs about its persistence play key roles in shaping their experience of pain and PD (
15). Despite the chronic nature of pain and its significant life disruptions, the role of psychological time remains largely unexplored (
16). Psychological distress, a key psychological concern linked to pain, affects various health outcomes (
17). It encompasses a range of emotional states, primarily those related to depression and anxiety (
18). As a concept, distress is positively associated with both poor mental health and clinical psychological disorders, making it an important measure in assessing general well-being (
19).
Beyond its connection to pain, PD emerges as a significant factor in absenteeism and recovery (
20). Unseld et al. (
21) found that 63.5% of cancer patients experienced pain, with 31.2% showing significant PTSD, and notable levels of depression, anxiety, and distress in 13.9%, 15.1%, and 25.3% of patients, respectively. Women were more likely to report these symptoms. Dany et al. (
18) also identified a significant relationship between PD and CP, finding that patients with disorganized thoughts reported higher distress and greater pain intensity.
Patients with CP face an uncertain future, unsure of when or if they will find relief from their illness and the associated disability (
22). This ambiguity can lead to feelings of learned helplessness (LH) and ineffective coping mechanisms (
23). Learned helplessness is particularly important in understanding the high rates of depression and functional limitations observed among CP patients (
24). It is characterized by an attributional style in which individuals perceive minimal control over life events, leading them to respond passively to challenges (
25,
26). Patients may feel incapable of effecting change despite their best efforts, resulting in a passive attitude toward their illness (
27). This feeling often stems from multiple failed attempts to manage their pain. In CP cases, even with proper treatment, results may not be rapid or satisfactory (
28). Learned helplessness closely correlates with depression due to their shared attributional process regarding negative events (
29).
As a result, individuals experiencing negative situations may attribute them to their inability to manage the situation, believing this inability is unlikely to improve (
30). Moyano et al. (
25) conducted a cross-sectional study comparing LH and perceived self-efficacy in patients with fibromyalgia (FM) and rheumatoid arthritis (RA), examining their associations with functional disability, pain levels, and fatigue. Among 215 patients, FM patients exhibited higher levels of LH and depression but lower self-efficacy than RA patients. Similarly, Nowicka-Sauer et al. (
24) explored the relationship between LH and illness perception, depression, and anxiety among lupus patients. They found that LH was positively correlated with illness perception, depression, and anxiety, suggesting a connection between LH and psychological factors in lupus patients.