Abstract
Background
To promote health-related quality of life (HRQOL) in adolescents with pain, it is important to study factors associated with pain. This study aimed to describe selected factors and pain in 14–15-year-old adolescents and their parents, to assess how these factors are associated with adolescent pain groups, and to explore whether the relationship between pain intensity and HRQOL in adolescents with persistent pain is mediated by self-esteem and self-efficacy.
Methods
A cross-sectional study was performed among 508 dyads of adolescents (14–15 years) and parents in a school-based setting. Among these, 148 adolescents had persistent pain. We explored the following variables: HRQOL, pain, self-efficacy, self-esteem, sleep, loneliness, stress and sociodemographic variables. All variables were assessed with well-validated instruments. HRQOL was measured with KIDSCREEN-27. Analyses included Chi-square, ANOVA, Mann–Whitney U tests, Kruskal–Wallis and the PROCESS macro method for mediation analyses.
Results
Adolescents with pain reported significantly higher levels of stress, loneliness and lack of sleep and lower levels of self-efficacy, self-esteem and HRQOL compared to adolescents without pain. More girls than boys reported pain. Adolescents with persistent pain scored significantly worse on self-esteem, stress, loneliness, lack of sleep, school absence, pain and HRQOL compared to adolescents with shorter pain duration. Adolescent pain groups did not differ significantly considering parental factors. However, more adolescents with persistent pain reported that someone in their family had pain. The associations between pain intensity and the HRQOL subscales in adolescents with persistent pain were completely mediated by self-esteem, but not by self-efficacy. The highest degree of mediation was estimated for the HRQOL subscale school environment (indirect effect = 73.5%).
Conclusions
Our findings highlight the complexity within adolescent pain, demonstrating that adolescents with pain differ from adolescents without pain when it comes to gender, school absence, factors within-person and between-persons. Longer pain duration makes adolescents more vulnerable. We confirm the importance of resilience factors for HRQOL but indicate that self-esteem is more important than self-efficacy. To promote HRQOL in adolescents with persistent pain, a strengthening of both their self-esteem and self-efficacy is recommended. We highlight the need for an individual, holistic approach to adolescent pain.
Supplementary Information
The online version contains supplementary material available at 10.1186/s40359-021-00629-z.
Keywords: Persistent pain, Health-related quality of life, Adolescents, Parents, Self-efficacy, Self-esteem, Resilience, Mediation
Introduction
Pain problems in adolescents have increased during the last 2 decades and is recognized as a substantial public health challenge in industrialized countries [1, 2]. Negative consequences of adolescent pain include peer relationship problems, sleeping problems, avoidance of activities and sports, school absenteeism, an increased risk of recurrent pain in adulthood and a decreased health-related quality of life (HRQOL) [3–9]. The term HRQOL is a multidimensional construct that includes the individual’s subjective perspectives on the physical, psychological, social and functional aspects of health [10]. By measuring HRQOL in adolescents with pain, one can gain insight into adolescents’ subjective experiences of pain and how pain affects different dimensions of their lives [11].
According to the International Association for the Study of Pain, pain is always a personal experience that is influenced by biological, psychological, and social factors [12]. Adolescents communicate pain more and less clearly, and causal factors range from identifiable to very diffuse [10]. Sociodemographic factors [e.g. age, gender, ethnicity, socioeconomic status (SES)] and factors within-person (e.g. stress, self-efficacy, self-esteem, sleeping problems) and between-persons (e.g. parents/family, loneliness, the school situation) contribute to and affect adolescent pain from both a resilience perspective and a risk perspective [2, 4, 8, 13–22]. Further, studies have shown that a history of pain in their parents may increase adolescent risk for chronic pain [14, 15, 23].
Internationally comparable data suggest persistent or chronic pain among adolescents in different countries is highly prevalent [24]. Chronic pain is defined as persistent or recurrent pain lasting longer than 3 months [25]. Persistent pain has consequences for the individual, their family and the society at large [19, 26–28]. More knowledge on factors that characterize adolescents with and without pain in a non-clinical population is necessary to better understand the cause of pain problems and find the best strategies to help adolescents with pain. Moreover, knowledge of whether there are factors in adolescents with persistent pain that differ from factors in adolescents with pain lasting less than 3 months is needed.
Adolescent pain research has mainly focused on maladjustment and risk factors. Thus, shifting the focus to protective and resilience factors has been recommended [18, 29, 30]. The term resilience refers to the state of an individual having a relatively good psychological outcome despite the presence of risk factors [31]. Both self-esteem and self-efficacy are considered resilient factors [22, 32, 33]. Self-esteem represents one’s positive or negative attitude toward oneself [34], whereas self-efficacy represents a self-confident view of one’s capability to deal with certain stressors in life [32]. Studies have shown that self-efficacy and self-esteem have a positive impact on both pain and HRQOL in adolescents [18, 35–43]. Higher levels of self-efficacy and self-esteem may protect an adolescent from experiencing pain, it can help to positively adapt and cope with pain, and it is associated with higher levels of HRQOL despite having pain [18, 22, 38, 41, 42].
There is a wide variety and complexity within adolescent pain, and it is therefore important to understand pain in light of a holistic model [11], such as the multidimensional biobehavioral model of pediatric pain [44, 45]. This model illustrates that pain may arise from several precipitants (such as disease, injury or stress) and that potentially modifiable intervening variables can influence both pain and HRQOL. According to this model, these intervening variables are biological predispositions (e.g. genetics, age, gender), family environment (e.g. family functioning, family pain models), perceived social support, cognitive appraisal and coping strategies [44, 45]. Inspired by the model, the present study focused on selected factors in adolescents (sociodemographic characteristics, self-efficacy, self-esteem, loneliness, stress, sleep, HRQOL and pain characteristics) and in their parents (sociodemographic characteristics, HRQOL, parental pain characteristics) that previous research has identified as being associated with adolescent pain [2, 4, 8, 13–22]. These factors can be viewed as both precipitants and intervening variables within the model. More knowledge of these factors in adolescents might shed light on the complexity of adolescent pain. Moreover, because we consider self-efficacy and self-esteem as highly relevant intervening factors within the model, we focused on the possible mediating effect of self-efficacy and self-esteem on the relationship between pain and HRQOL in adolescents with persistent pain.
This study aimed to describe selected sociodemographic- and psychosocial factors and pain in 14–15-year-old adolescents and their parents. Further, to assess how these factors were associated with adolescent pain groups (no pain, pain lasting less than 3 months, persistent pain). Lastly, to explore whether the relationship between pain intensity and HRQOL in adolescents with persistent pain is mediated by self-esteem and/or self-efficacy.
Methods
Sample and data collection
The present study was conducted from November 2018 to April 2019 in the south-eastern part of Norway as part of the “Start Young—Quality of Life and Pain in Generations” study [43]. Schools covering ninth grade in elementary school (students aged 14–15 years) were stratified according to geographical region, school size, urban and rural districts. Two schools were randomly selected from each such stratum and invited to participate. Schools that declined were replaced by other schools selected according to the same criteria. In total, 22 schools that varied in size and localization participated. Project members visited participating schools to provide the adolescents with verbal and written information about the study. Parents received written information. Active informed consent was obtained from both adolescents and their parents. Potential participants in the study were 1663 adolescent–parent dyads from the participating schools. In total, 696 adolescents (41.8%) and 561 parents (33.7%) filled in the questionnaire. In this study, we included the 508 adolescent–parent dyads (30.5% of the invited) with responses from both adolescents and one of their parents. The response rate varied across schools, from 2.9 to 71.1%.
The data collection was done through a web-based questionnaire. Adolescents completed the questionnaire in classroom during school hours. Parents received a mail with a safe link to the questionnaire and completed the questionnaire at home. A safe data server was used to store the collected data [46]. Information from the parents’ consent form enabled us to link the questionnaires from the adolescents with their parents’ questionnaires by creating a mutual ID number.
All study procedures were approved by the Norwegian Centre for Research Data (Ref:60981).
Measures
The study used an electronic survey tool that consecutively administered the following questionnaires. Most questions included a neutral option. This resulted in all items being answered. Thirteen variables that had several categories were recoded into fewer categories. This is explained in Tables 1 and 2. All questionnaires that use sum scales showed satisfactory values of Cronbach’s alpha above 0.7 in the present study (Additional file 1).
Table 1.
Total (N = 508) | No pain (n = 124) | Pain < 3 months (n = 236) | Persistent pain (n = 148) | p value | |
---|---|---|---|---|---|
Adolescent characteristics | |||||
Gender, N (%) | < .0011,2 | ||||
Female | 281 (55.3) | 42 (33.9) | 141 (59.7) | 98 (66.2) | |
Male | 227 (44.7) | 82 (66.1) | 95 (40.3) | 50 (33.8) | |
Age, median (min, max) | 14.0 (14.0, 15.0) | 14.0 (14.0, 15.0) | 14.0 (14.0, 15.0) | 1.0 (14.0, 15.0) | .447 |
Adult members of the household, N (%)a | .204 | ||||
Both parents | 381 (75.0) | 99 (79.8) | 176 (74.6) | 106 (71.6) | |
Alternates between two parents | 68 (13.4) | 15 (12.1) | 27 (11.4) | 26 (17.6) | |
One parent and/or other caregivers | 59 (11.6) | 10 (8.1) | 33 (14.0) | 16 (10.8) | |
Parents’ work status, N (%)b | .246 | ||||
Both parents are working | 414 (81.5) | 104 (83.9) | 196 (83.1) | 114 (77.0) | |
One parent is working | 94 (18.5) | 20 (16.1) | 40 (16.9) | 34 (23.0) | |
School absence for the previous 3 months, N (%)c | .0162 | ||||
No absence | 180 (35.4) | 54 (43.5) | 78 (33.1) | 48 (32.4) | |
1–4 days | 259 (51.0) | 60 (48.4) | 129 (54.7) | 70 (47.3) | |
≥ 5 days | 69 (13.6) | 10 (8.1) | 29 (12.3) | 30 (20.3) | |
Parent characteristics | |||||
Gender, N (%) | .568 | ||||
Female | 393 (77.4) | 95 (76.6) | 179 (75.8) | 119 (80.4) | |
Male | 115 (22.6) | 29 (23.4) | 57 (24.2) | 29 (19.6) | |
Age, mean (SD) | 45.2 (4.9) | 45.4 (4.5) | 45.2 (4.9) | 45.2 (5.1) | .923 |
Marital status, N (%)d | .195 | ||||
Married/cohabitant | 422 (83.1) | 109 (87.9) | 195 (82.6) | 118 (79.9) | |
Single/divorced | 86 (16.9) | 15 (12.1) | 41 (17.4) | 30 (20.3) | |
Education level, N (%)e | .697 | ||||
≤ 12 years and/or certificate of apprenticeship | 127 (25.0) | 28 (22.6) | 59 (25.0) | 40 (27.0) | |
13–15 years (< 4 years of higher education) | 129 (25.4) | 32 (25.8) | 65 (27.5) | 32 (21.6) | |
≥ 16 years (≥ 4 years of higher education) | 252 (49.6) | 64 (51.6) | 112 (47.5) | 76 (51.4) | |
Work status, N (%) | .297 | ||||
Yes, full time | 375 (73.8) | 83 (66.9) | 181 (76.7) | 111 (75.0) | |
Yes, part time | 91 (17.9) | 30 (24.2) | 36 (15.3) | 25 (16.9) | |
No, not employed | 42 (8.3) | 11 (8.9) | 19 (8.1) | 12 (8.1) | |
Household income, N (%)f | .527 | ||||
≤ 450,000 NOK/year | 44 (8.7) | 9 (7.3) | 20 (8.5) | 15 (10.1) | |
451,000–750,000 NOK/year | 88 (17.3) | 18 (14.5) | 49 (20.8) | 21 (14.2) | |
751,000–1,000,000 NOK/year | 116 (22.8) | 33 (26.6) | 51 (21.6) | 32 (21.6) | |
> 1,000,000 NOK/year | 260 (51.2) | 64 (51.6) | 116 (49.2) | 80 (54.1) |
Bold values indicates statistically significant differences between the groups (p ≤ 0.05)
Continuous variables analyzed with ANOVA with Tukey’s HSD post hoc test or Kruskal–Wallis and Mann–Whitney U tests between pairs of groups
Categorical variables analyzed with x2-test. Significant differences between the marked groups: 1No pain versus Pain < 3 months, 2No pain versus Persistent pain and 3Pain < 3 months versus Persistent pain. p values marked with bold indicate statistically significant differences between the groups (p ≤ 0.05)
The pain group variable was recoded into three categories: “No pain,” “Pain < 3 months” (only once, < 1 month, 1–3 months) or “Persistent pain” (> 3 months, > 6 months, > 12 months)
SD standard deviation, PCS physical component summary, MCS mental component summary
aThe variable was recoded into three categories: “Both parents,” “Alternates between two parents” or “One parent and/or other caregivers” (one parent and one step-parent, one parent, other caregivers)
bThe variable was dichotomized as “Both parents are working” or “One parent is working” (one parent is working, no parents are working)
cThe variable was recoded into three categories: “No absence,” “1–4 days” or “≥ 5 days” (5–7 days, 8–10 days, > 10 days)
dThe variable was dichotomized as “Married/cohabitant” or “Single/divorced” (single, divorced, widowed)
eThe variable was recoded into three categories: “≤ 12 years and/or certificate of apprenticeship” (9 years, 10–11 years, 12 years, certificate of apprenticeship), “13–15 years (< 4 years of higher education)” or “≥ 16 years (≥ 4 years of higher education)”
fthe variable was recoded into four categories: “≤ 450,000 NOK/year” (< 250,000 NOK/year, 250,000–450,000 NOK/year), “451,000–750,000 NOK/year,” “751,000–1,000,000 NOK/year” or “> 1,000,000 NOK/year.”
Table 2.
Total (N = 508) | No pain (n = 124) | Pain < 3 months (n = 236) | Persistent pain (n = 148) | p value | |
---|---|---|---|---|---|
Adolescent characteristics | |||||
Physical well-being, mean (SD)a,b | 47.4 (9.3) | 51.2 (10.0) | 47.4 (8.4) | 44.2 (9.4) | < .0011,2,3 |
Psychological well-being, mean (SD)a,b | 46.6 (8.6) | 52.3 (8.2) | 46.1 (7.0) | 42.7 (8.6) | < .0011,2,3 |
Autonomy and parent relations, mean (SD)a,b | 52.8 (8.7) | 56.7 (9.0) | 52.4 (8.0) | 50.2 (8.6) | < .0011,2,3 |
Social support and peers, mean (SD)a,b | 48.3 (8.4) | 50.6 (8.3) | 48.1 (8.2) | 46.7 (8.6) | 0.0041,2 |
School environment, mean (SD)a,b | 48.2 (8.8) | 52.5 (9.6) | 47.6 (8.2) | 45.6 (7.9) | < .0011,2 |
Self-efficacy, mean (SD)c | 3.1 (0.4) | 3.2 (0.4) | 3.1 (0.4) | 3.0 (0.4) | < .0011,2 |
Self-esteem, median (min, max)d | 3.0 (1.0, 4.0) | 3.5 (1.7, 4.0) | 3.0 (1.0, 4.0) | 3.0 (1.0, 4.0) | < .0011,2,3 |
Loneliness, median (min, max)e | 12 (8, 32) | 11 (8, 21) | 13 (8, 32) | 14 (8, 32) | < .0011,2,3 |
Stress, mean (SD)f | 0.29 (0.16) | 0.20 (0.12) | 0.29 (0.15) | 0.36 (0.17) | < .0011,2,3 |
Frequency of enough sleep N (%)g | < .0011,2,3 | ||||
Usually/always | 329 (64.9) | 101 (82.1) | 152 (64.4) | 76 (51.4) | |
Sometimes/rarely | 178 (35.1) | 22 (17.9) | 84 (35.6) | 72 (48.6) | |
Problems with sleepiness N (%)h | < .0011,2,3 | ||||
No | 213 (42.0) | 81 (65.9) | 98 (41.5) | 34 (23.0) | |
Yes | 294 (58.0) | 42 (34.1) | 138 (58.5) | 114 (77.0) | |
Parent characteristics | |||||
RAND-36 PCS, mean (SD)i | 51.5 (9.0) | 52.0 (8.6) | 51.4 (9.1) | 51.4 (9.1) | .803 |
RAND-36 MCS, mean (SD)i | 52.4 (8.0) | 53.7 (7.3) | 51.8 (8.6) | 52.3 (7.6) | .106 |
Bold values indicates statistically significant differences between the groups (p ≤ 0.05)
Continuous variables analyzed with ANOVA with Tukey’s HSD post hoc test or Kruskal–Wallis and Mann–Whitney U tests between pairs of groups
Categorical variables analyzed with x2-test. Significant differences between the marked groups: 1No pain versus Pain < 3 months, 2No pain versus Persistent pain and 3Pain < 3 months versus Persistent pain. p values marked with bold indicate statistically significant differences between the groups (p ≤ 0.05)
The pain group variable was recoded into three categories: “No pain,” “Pain < 3 months” (only once, < 1 month, 1–3 months) or “Persistent pain” (> 3 months, > 6 months, > 12 months)
SD standard deviation, PCS physical component summary, MCS mental component summary
aKIDSCREEN subscales
bRasch scores were computed for each subscale and transformed into t-values with a mean of 50 and an SD of 10. Higher values indicate higher levels of HRQOL
cRange 1–4, where higher values indicate higher levels of self-efficacy
dRange 1–4, where higher values indicate higher levels of self-esteem
eRange 8–32, where higher values indicate higher levels of loneliness
fRange 0–1, where higher values indicate higher levels of stress
gThe variable was dichotomized as “Usually/always” (usually, always) or “Sometimes/rarely” (sometimes, rarely, never)
hThe variable was dichotomized as “No” or “Yes” (a slight problem, more than a slight problem, a big problem, a very big problem)
iRAND-36 scores range from 0 to range 0–100, where 100 means perfect health
The first part of the survey contained sociodemographic information. Adolescents answered questions about gender, age, adult members of the household, parents’ birthplace, parental work status and school absence. Parents answered questions about age, gender, marital status, education level, work status and household income. We used the variables regarding adult members of the household, parental education level and household income to indicate SES in further analyses.
Pain in adolescents and in parents was assessed using the Brief Pain Inventory (BPI), which asks participants to rate the subjective intensity of pain at its worst, least and in average, and how pain interferes with different aspects of life [47, 48]. Adolescents and parents answered questions about their own pain experiences. The items are presented as numeric rating scales, with 0 = no pain to 10 = pain as bad as you can imagine. For analysis, the interference items were combined into two indexes of interference: activity and emotions [47]. The Norwegian BPI has satisfactory psychometric properties and has been used among both adolescents and adults [48, 49]. We also used selected questions from the Lübeck Pain-Screening Questionnaire (LPQ), which assesses the presence and consequences of pain during the preceding 3 months [50]. Adolescents and parents were asked about pain duration and pain frequency. To be able to assess how selected factors were associated with adolescent pain groups, we used the adolescents’ pain duration variable to divide adolescents into three different groups. The variable was recoded into: “no pain,” “pain < 3 months” (only once, < 1 month or 1–3 months) or “persistent pain” (> 3 months, > 6 months or > 12 months). Additionally, the adolescents were asked about self-perceived triggers of pain. A list of possible causes (presented in the footnotes of Table 3) was derived from the LPQ questionnaire [50] and the adolescents were asked to tick all possible causes. The Norwegian LPQ has demonstrated satisfactory content validity and high internal consistency [8]. Only those who rated ≥ 1 on the “pain on average” question from the BPI (indicating that they had pain) were administered questions about pain interference (from the BPI) and questions about pain duration, frequency and self-perceived triggers of pain (from the LPQ). Finally, we used two questions derived from the Norwegian “Pain, Youth and Self-Medication study” [51, 52] to measure the intake of over-the-counter (OTC) analgesics in adolescents and in parents. First, the respondents were asked about OTC analgesic intake during the last 4 weeks. If they answered “yes,” they were asked about the frequency of intake.
Table 3.
Total (N = 508) | No pain (n = 124) | Pain < 3 months (n = 236) | Persistent pain (n = 148) | p value | |
---|---|---|---|---|---|
Adolescent characteristics | |||||
Pain worst, median (min, max)a | 3.0 (0.0, 10.0) | 0.0 (0.0, 10.0) | 3.0 (0.0,9.0) | 5.0 (0.0, 10.0) | < .0011,2,3 |
Pain least, median (min, max)a | 0.0 (0.0, 8.0) | 0.0 (0.0, 5.0) | 1.0 (0.0, 8.0) | 1.0 (0.0, 6.0) | < .0011,2 |
Pain average, median (min, max)a | 2.0 (0.0, 10.0) | 0.0 (0.0, 3.0) | 2 (1.0, 10.0) | 3 (1.0, 9.0) | < .0011,2,3 |
Pain interference on activity, median (min, max)b,c | 1.3 (0.0, 10.0) | 1.0 (0.0, 10.0) | 1.7 (0.0, 9.0) | < .0013 | |
Pain interference on emotions, median (min, max)b,c | 1.2 (0.0, 9.2) | 1.0 (0.0, 9.0) | 1.4 (0.0, 9.2) | .0023 | |
Pain frequency, N (%)b,d | < .0013 | ||||
Seldom | 159 (41.4) | 148 (62.7) | 11 (7.4) | ||
Sometimes | 90 (23.4) | 49 (20.8) | 41 (27.7) | ||
Often | 135 (35.2) | 39 (16.5) | 96 (64.9) | ||
Self-perceived triggers of painb,e | |||||
Emotions | 78 (20.3) | 44 (18.6) | 34 (23.0) | .305 | |
School | 97 (25.3) | 52 (22.0) | 45 (30.4) | .066 | |
Lack of sleep | 99 (25.8) | 59 (25.0) | 40 (27.0) | .659 | |
Cold/illness | 58 (15.1) | 45 (19.1) | 13 (8.8) | .0063 | |
Digital technology use | 50 (13.0) | 28 (11.9) | 22 (14.9) | .395 | |
Loneliness | 115 (29.9) | 58 (24.6) | 57 (38.5) | .0043 | |
Sport/physical activities | 33 (8.6) | 18 (7.6) | 15 (10.1) | .393 | |
Menstruationf | 85 (35.6) | 51 (36.2) | 34 (34.7) | .815 | |
Other | 200 (52.1) | 115 (48.7) | 85 (57.4) | .097 | |
Family members having pain, N (%) | < .0012,3 | ||||
Yes | 154 (30.4) | 26 (21.1) | 63 (26.7) | 65 (43.9) | |
Do not know | 198 (39.1) | 44 (35.8) | 100 (42.4) | 54 (36.5) | |
No | 155 (30.6) | 53 (43.1) | 73 (30.9) | 29 (19.6) | |
OTC analgesic intake during the last 4 weeks, N (%) | .0011,2 | ||||
Yes | 242 (47.7) | 41 (33.3) | 118 (50.0) | 83 (56.1) | |
No | 265 (52.3) | 82 (66.7) | 118 (50.0) | 65 (43.9) | |
Frequency of OTC analgesic intake, N (%)g,h | .674 | ||||
Every week | 48 (19.8) | 7 (17.1) | 22 (18.6) | 19 (22.9) | |
Less often than every week | 194 (80.2) | 34 (82.9) | 96 (81.4) | 64 (77.1) | |
Parent characteristics | |||||
Pain worst, median (min, max)a | 2.0 (0.0, 10.0) | 1.0 (0.0, 10.0) | 2.0 (0.0, 10.0) | 2.0 (0.0, 9.0) | .138 |
Pain least, median (min, max)a | 0.0 (0.0, 9.0) | 0.0 (0.0, 5.0) | 0.0 (0.0, 9.0) | 0.0 (0.0, 9.0) | .529 |
Pain on average, median (min, max)a | 1.0 (0.0, 10.0) | 1.0 (0.0, 9.0) | 1.0 (0.0, 9.0) | 1.0 (0.0, 6.0) | .692 |
Pain interference on activity, median (min, max)c,i | 0.7 (0.0, 10.0) | 0.3 (0.0, 9.0) | 0.7 (0.0, 10.0) | 0.7 (0.0, 8.0) | .518 |
Pain interference on emotions, median (min, max)c,i | 1.0 (0.0, 10.0) | 0.5 (0.0, 9.0) | 1.0 (0.0, 10.0) | 1.0 (0.0, 8.0) | .465 |
Pain frequency, N (%)d,i | .944 | ||||
Seldom | 87 (28.2) | 20 (27.4) | 40 (27.6) | 27 (30.0) | |
Sometimes | 58 (18.8) | 13 (17.8) | 30 (20.7) | 15 (16.7) | |
Often | 163 (52.9) | 40 (54.8) | 75 (51.7) | 48 (53.3) | |
Pain duration, N (%)i,j | .963 | ||||
No pain | 200 (39.4) | 51 (41.1) | 91 (38.6) | 58 (39.2) | |
Pain < 3 months | 100 (19.7) | 24 (19.4) | 49 (20.8) | 27 (18.2) | |
Persistent pain | 208 (40.9) | 49 (9.6) | 96 (40.7) | 63 (42.6) | |
OTC analgesic intake during the last 4 weeks, N (%) | .661 | ||||
Yes | 296 (58.3) | 68 (54.8) | 141 (59.7) | 87 (58.8) | |
No | 212 (41.7) | 56 (45.2) | 95 (49.3) | 61 (41.2) | |
Frequency of OTC analgesic intake, N (%)h,k | .587 | ||||
Every week | 96 (32.4) | 21 (30.9) | 43 (30.5) | 32 (36.8) | |
Less often than every week | 200 (67.6) | 47 (69.1) | 98 (69.5) | 55 (63.2) |
Bold values indicates statistically significant differences between the groups (p ≤ 0.05)
Continuous variables analyzed with Mann–Whitney U test or Kruskal–Wallis with Mann–Whitney U tests between pairs of groups
Categorical variables analyzed with x2-test. Significant differences between the marked groups: 1No pain versus Pain < 3 months, 2No pain versus Persistent pain and 3Pain < 3 months versus Persistent pain. p values marked with bold indicate statistically significant differences between the groups (p ≤ 0.05)
The pain group variable was recoded into three categories: “No pain,” “Pain < 3 months” (only once, < 1 month, 1–3 months) or “Persistent pain” (> 3 months, > 6 months, > 12 months)
OTC over the counter
aRange 0–10, where 10 indicates pain as bad as you can imagine
bN = 384
cRange 0–10, where 10 indicates complete interference of pain
dThe variable was recoded into three categories: “seldom” (< once/month, once/month), “sometimes” (2–3 times/month, once/week) or “often” (several times/week, every day)
eThe variable was recoded into nine categories: “Emotions” (anger/disputes, sadness, agitation), “School” (school situation, school work), “Lack of sleep,” “Cold/illness,” “Digital technology use” (social media, screen time), “Loneliness,” “Sport/physical activities,” “Menstruation” and “Other” (change of weather, noise, family condition, a new situation, nutrition/sweets, nonspecific factors)
fN = 239 (only girls were asked about this possible trigger of pain)
gN = 242
hThe variable was dichotomized as “Every week” (daily, every week but not daily) or “Less often than every week” (less often than every week, no intake)
iN = 308
jThe variable was recoded into three categories: “No pain,” “Pain < 3 months” (only once, < 1 month, 1–3 months) or “Persistent pain” (> 3 months, > 6 months, > 12 months)
kN = 296
HRQOL in adolescents was assessed using the KIDSCREEN-27 questionnaire [53, 54]. The KIDSCREEN-27 is a multidimensional measure of generic HRQOL and consists of 27 questions grouped into five subscales: (1) physical well-being, (2) psychological well-being, (3) autonomy and parent relations, (4) social support and peers and (5) school environment [53, 55, 56]. The KIDSCREEN questionnaire is scored on a 1–5 Likert scale referring to the last week. The scale indicates either the intensity of an attitude or the frequency of certain behaviors or feelings. In line with the KIDSCREEN-handbook [55], Rasch scores were computed for each subscale and transformed into t-values that can be compared with international t-values. These t-values are normed to a mean (SD) of 50 (10) [55]. The answers were recoded so that higher scores indicate better HRQOL. The Norwegian version of the KIDSCREEN-27 has been shown to be reliable and valid [54].
HRQOL in parents was assessed using the 36-item Medical Outcomes Study Short Form (RAND-36), which consists of eight domains (general health, bodily pain, physical function, role limitations [physical], mental health, vitality, social function and role limitations [emotional]). These eight domains can be combined into a physical component summary scale (PCS) and a mental component summary scale (MCS), which reflect physical and mental health, respectively [57, 58]. We used the PCS and MCS scales in this study. The RAND-36 scales were scored according to recommended scoring procedures, and sum scales were expressed using values from 0 to 100, with 100 representing excellent health [57, 58].
Self-efficacy in adolescents was assessed using the 10-item Generalized Self‐Efficacy scale (GSE), which measures optimistic self-beliefs in coping with the tasks, demands and challenges of life in general [59, 60]. The scale includes 10 statements that the respondent rates on a 1–4-point scale. The respondent’s scores on each item are summed and divided by 10 to obtain a GSE score ranging from 1 to 4. Higher scores indicate higher levels of GSE. The GSE has been found to be valid and reliable, with satisfactory internal consistency [40, 59].
Self-esteem in adolescents was assessed using the four-item version of the Rosenberg Self-Esteem Scale (RSES) [61, 62] consisting of four statements on self-perceptions related to attitude toward oneself, feeling of uselessness, having something to be proud of, and self-worth. RSES is rated on a 1–4 Likert scale. Scores are summed and divided by 4 to obtain a RSES score ranging from 1 to 4, where higher scores represent higher self-esteem. The four-item version correlates highly with the original 10-item version (0.95) [62], which is considered a valid measure of self-esteem in a large body of literature. The four-item version has previously been used among Norwegian adolescents and has good internal consistency [63–65].
Loneliness in adolescents was assessed using the eight-item version of the revised UCLA Loneliness Scale (ULS-8), which is considered to be a reliable and adequate measure of loneliness among adolescents [66–68]. The eight items are rated on a 1–4-point scale, with values ranging from “never” to “always.” The total score ranges from 8 to 32 points, with higher scores indicating higher levels of loneliness. The Norwegian version of ULS-8 has been found reliable with satisfactory internal consistency [43].
Stress in adolescents was assessed using the 30-item Perceived Stress Questionnaire (PSQ) [69–71]. PSQ refers to the last 4 weeks and is rated on a 4-point rating scale. PSQ contains both negatively and positively formulated items to reduce acquiescent bias. The answers were recoded so that higher scores indicate higher levels of perceived stress. The resulting PSQ total score is transformed linearly between 0 and 1: PSQ = (raw value − 30)/90. Commonly applied cutoff levels of stress within PSQ are low: < 0.33, medium: 0.33–0.45, moderate: 0.45–0.60 and severe: > 0.60 [69]. The Norwegian version of PSQ has shown good reliability and validity [71].
Sleep was assessed using two questions derived from the School Sleep Habits Survey, which has been widely used in adolescents [72]. We used one question focusing on frequency of enough sleep and one focusing on problems with sleepiness during daily activities. The School Sleep Habits Survey has an established validity compared to sleep diaries and actigraphy [73] and has previously been used among Norwegian adolescents [74].
Data analyses
The statistical analyses were conducted using IBM SPSS Statistics (version 26.0). Descriptive statistics were calculated for all variables according to three previously defined adolescent pain groups. Continuous variables were described with mean and standard deviation or as median and min/max, categorical variables with counts and percentages. Strength of associations between pairs of selected variables was assessed using chi-square test for categorical data and ANOVA with Tukey’s HSD post hoc test or Kruskal–Wallis and Mann–Whitney U tests for continuous data. To fulfill the assumption of “minimum expected cell frequency” for chi-square analyses [75], some of the items that had several categories were recoded into fewer categories.
Mediation analyses were conducted using the PROCESS macro method developed for SPSS by Hayes [76]. We proceeded using the parallel multiple mediation model depicted in Fig. 1. PROCESS was used to estimate (1) the direct effect of pain on HRQOL (C′), (2) the total effect of pain on HRQOL (C) and (3) the specific indirect effects through mediator 1 (self-efficacy) and mediator 2 (self-esteem) (aibi). Gender, adult members of the household, parental education and household income were entered as covariates. Proportions mediated for the direct and indirect effects were estimated as the direct effect/total effect and the indirect effect/total effect and multiplied by 100 to be interpreted as percentages. The calculation of direct and total indirect effect as percentages was not applicable for the HRQOL subscales autonomy and parent relations and social support and peers due to opposite directions of the total effects and the direct effects. The mediation effect was considered statistically significant if the 95% confidence interval (CI) for the effect did not include zero. All the analyses were considered exploratory. Hence, no correction for multiple testing was done, and p values < 0.05 were considered significant. All the tests were two-sided. Assumptions for mediation analyses were checked and fulfilled. According to Preacher and Hayes, a significant indirect effect is no longer seen as a prerequisite for mediation [77]. Thus, all HRQOL subscales were included.
Results
Descriptive data for sociodemographic variables in adolescents and their parents
In total, 508 dyads of adolescents with one parent each participated in the study. The majority were girls (55.3%) and mothers (77.4%), respectively. The adolescents’ ages ranged from 14 to 15 years, with a median age of 14 years. The mean (SD) age for the parents were 45.2 (4.9) years. Among the adolescents, 148 had persistent pain. The three adolescent pain groups were similar concerning all the selected sociodemographic variables in adolescents and their parents, except for adolescents’ gender and school absence (Table 1).
Descriptive data for adolescent- and parent pain-related factors
Descriptive data for adolescent- and parent pain-related factors by adolescent pain groups are presented in Table 2. Adolescents with pain lasting less than 3 months and persistent pain reported significantly higher levels of stress, loneliness and lack of sleep and lower levels of self-efficacy, self-esteem and HRQOL compared to adolescents without pain. Adolescents with persistent pain reported significantly lower HRQOL than adolescents with pain lasting less than 3 months for the KIDSCREEN subscales physical well-being, psychological well-being and autonomy and parent relations. Moreover, adolescents with persistent pain reported significantly lower levels of self-esteem and significantly higher levels of loneliness, stress and lack of sleep than adolescents with pain lasting less than 3 months. Considering the parents’ HRQOL, there were no statistically significant differences between the adolescent pain groups.
Descriptive pain characteristics of adolescents and parents
Table 3 shows the descriptive pain characteristics of adolescents and parents by adolescent pain groups (Table 3). Adolescents with persistent pain experienced pain significantly more often and reported significantly higher values of the worst pain and average pain compared to adolescents with pain lasting less than 3 months. Moreover, adolescents with persistent pain also reported significantly higher levels of pain interference in both activity and emotions.
The most prevalent self-perceived triggers of pain, as reported by the adolescents, were loneliness (29.9%), lack of sleep (25.8%) and school (25.3%). Girls also rated menstruation (35.6%) as a prevalent trigger of pain. More adolescents with persistent pain (38.5%) reported loneliness as a trigger compared to adolescents with pain lasting less than 3 months (24.6%).
Almost two-thirds of the adolescents and more than half of the parents with pain experienced pain in multiple body locations. Head pain and neck/shoulder pain were the most common pain locations for both adolescents and the parents. Among both adolescents and parents, about half reported intake of OTC analgesics during the last 4 weeks. Among these, almost one-third of the parents reported intake every week, while about 20% of the adolescents reported intake every week. Our univariate analyses showed no significant relationship between the adolescents’ and their parents’ use of OTC analgesics.
There were no statistically significant differences between the adolescent pain groups concerning any of the parents’ pain characteristics. However, more adolescents with persistent pain (43.9%) reported that someone in their family had pain compared to adolescents with pain lasting less than 3 months (26.7%) and adolescents without pain (21.1%).
Mediation by self-efficacy and self-esteem on the relationship between pain intensity and HRQOL in adolescents with persistent pain
We have suggested a parallel multiple mediation by self-efficacy (M1) and self-esteem (M2) of the association between pain intensity (X) and the scores for HRQOL subscales (Y) in adolescents with persistent pain, as depicted in Fig. 2. Unstandardized estimates of the Bs of the associated variables are depicted in the figure. We found that pain was associated with decreased self-efficacy (a1 = − 0.04) and self-esteem (a2 = − 0.13). However, the associations were only significant for self-esteem. Further, we found that having a higher self-efficacy score (b1) was significantly associated with higher HRQOL scores for the subscales physical well-being (b1 = 4.65) and school environment (b1 = 5.25). Moreover, we found that having a higher self-esteem score (b2) was significantly associated with higher HRQOL scores for all the subscales: physical well-being (b2 = 3.43), psychological well-being (b2 = 7.00), autonomy and parent relations (b2 = 3.37), social support and peers (b2 = 4.45) and school environment (b2 = 4.25).
The total effect (C) of pain on HRQOL was statistically significant for the subscales physical well-being (C = − 1.37), psychological well-being (C = − 1.52) and school environment (C = − 1.03). This indicates that for these subscales, an increased pain score is associated with a decreased HRQOL score after adjusting for the two mediators and holding the covariates gender, adult members of the household, parental education and household income constant. The direct effect (C′) of pain on HRQOL was no longer statistically significant for any of the subscales, indicating that the association were completely mediated by self-efficacy and self-esteem.
Table 4 shows the reduction in HRQOL subscales (presented as percentages) in adolescents with persistent pain explained by the direct (pain intensity) and indirect (self-efficacy and self-esteem) effects. Self-efficacy was not a mediator in the relationship between pain and HRQOL. Self-esteem completely mediated the relationship between pain and HRQOL for the subscales physical well-being, psychological well-being and school environment. More than half of the reductions in the HRQOL subscale scores for psychological well-being and school environment, and about one-third of the reduction for physical well-being were explained by the mediating variable self-esteem. Among the five HRQOL subscales, the total indirect effect was highest for the subscale school environment (73.5%).
Table 4.
Direct effect | Indirect effect of self-efficacy | Indirect effect of self-esteem | Total indirect effecta | |
---|---|---|---|---|
Physical well-beingb | 54.2% | 13.7% | 32.1%* | 45.8%* |
Psychological well-beingb | 35.4% | 5.7% | 58.8%* | 64.6%* |
Autonomy and parent relationb | – | – | – | – |
Social support and peersb | – | – | – | – |
School environmentb | 26.5% | 20.5% | 53.0%* | 73.5%* |
HRQOL health-related quality of life
*Statistically significant; the 95% confidence interval for the effect did not include zero
aThe specific indirect effect of self-efficacy + the specific indirect effect of self-esteem (a1b1 + a2b2)
bKIDSCREEN subscales
Discussion
Overall, we believe our findings support the need to understand pain through a holistic model such as the multidimensional biobehavioral model of pediatric pain [44, 45]. In light of this model, self-esteem, self-efficacy, stress, loneliness, sleep and sociodemographic factors might serve as both precipitants that pain may arise from and intervening variables that can influence both pain and HRQOL. Specifically, we believe our results highlight that self-esteem and self-efficacy should be considered as important intervening variables.
The complexity within adolescent pain
The current findings demonstrate the complexity within adolescent pain. We found that adolescents with pain differ from adolescents without pain when it comes to gender and school absence and factors within-person (self-efficacy, self-esteem, stress, sleeping problems) and between-persons (loneliness). Further, in line with previous studies [3, 38], this study shows that having pain is negatively associated with HRQOL, indicating that pain affects physical, psychological, social and functional aspects of adolescents’ lives. As highlighted in another Norwegian study [8], pain problems seem to have widespread and generally negative effects on several aspects of adolescents’ lives. We also found a wide variety considering the adolescents’ self-perceived triggers of pain, emphasizing the subjectivity within pain experiences.
Our results demonstrate that adolescents with persistent pain constitute a vulnerable group, as they reported higher levels of stress, loneliness, lack of sleep and lower levels of self-efficacy, self-esteem and HRQOL compared to adolescents with less pain. Negative findings related to having persistent pain have also been highlighted in other studies [4, 7, 22]. Further, our results indicate that a longer pain duration is making the adolescents more vulnerable to pain interference.
It is notable that in addition to reporting higher scores of loneliness, more adolescents with persistent pain reported loneliness as a self-perceived trigger of pain compared to adolescents with a shorter pain duration. This indicate that loneliness is a significant problem among adolescents with persistent pain. Our findings are in line with the review of Forgeron et al. [9], who found that adolescents with persistent pain have peer relationship deficiencies. Across studies, this review found that adolescents with persistent pain were viewed as more isolated than healthy peers, were reported to have fewer friends and may be subjected to more peer victimization. Loneliness is strongly associated with HRQOL in adolescents [43]. Thus, an increased awareness of peer relationship challenges for adolescents with persistent pain is very important.
The mediating role of self-esteem and self-efficacy on the relationship between pain and HRQOL in adolescents with persistent pain
The effect of pain on HRQOL was completely mediated by self-esteem but not by self-efficacy, indicating that self-esteem plays a more important role than self-efficacy on the relationship between pain and HRQOL. Our findings contrast with the study of Grasaas et al. [38], who found that the associations between pain intensity and several HRQOL subscales were mediated by self-efficacy in adolescents with persistent pain. However, unlike Grasaas et al.’s study, our study included self-esteem as a parallel mediator and controlled for gender as a possible confounder, which may explain the different results. Previous studies have found important gender differences among adolescents when it comes to pain, HRQOL, self-esteem and self-efficacy [13, 35, 38, 43]. This may explain our results.
The review of Cousins and colleagues ([18] pp. 843–844) highlights that “the concept of resilience empowers youth to foster their skills and strengths to positively adapt and live successfully with their pain,” and previous research have highlighted the importance of considering high self-esteem and self-efficacy as important protective or resource factors for HRQOL in adolescents [35–39, 43]. Our results confirm the importance of resilience factors for well-being in adolescents with persistent pain by showing that up to 73.5% of the reduction in the HRQOL subscale scores for physical well-being, psychological well-being and school environment could be explained by the mediating variables self-esteem and self-efficacy. Furthermore, the total indirect effect was highest for the HRQOL subscale school environment, indicating that self-esteem and self-efficacy especially play an important part in adolescents with pain’s well-being at school. Previous studies have found that low self-esteem relate to relative increases in loneliness over time and vice versa [78]. Peer relationship is important at school and adolescents experience relationships with peers as vital to their well-being [79]. Considering that loneliness was found to be a significant problem among the adolescents with persistent pain, this might explain our findings. Another noteworthy finding was that the associations between the HRQOL subscales and self-esteem were statistically significant for all five HRQOL subscales, while self-efficacy was only significantly associated with the subscales physical well-being and school environment. However, for these two subscales, self-efficacy had a higher effect than self-esteem. This shows that self-esteem and self-efficacy affect physical, psychological, social and functional aspects of adolescents’ lives in different ways, suggesting that both resilience factors are important for the well-being of adolescents.
Resilience factors such as self-esteem and self-efficacy are especially important during adolescence. The social and emotional development of adolescents is characterized by a struggle with sense of identity, where adolescents strive for independence from caregivers while becoming increasingly influenced by peers [80]. Support from family and friends is considered vital to enhance resilience [33]. To increase the sense of self-esteem and self-efficacy, Stewart and Yuen [33] recommends that individuals should be encouraged to think of other challenging situations they have mastered. According to their review, encouraging a sense of hope, realistic optimism and mastery over either the problem (e.g. pain) or one’s ability to cope with it might be helpful.
Family influence on adolescent pain
Parent history of pain may increase adolescent risk for chronic pain [14, 15, 23]. Surprisingly, our study found no differences between the adolescent pain groups considering any of the parents’ pain characteristics. However, more adolescents with persistent pain reported that someone in their family had pain, indicating that family history of pain still plays a significant role. It is possible that other elements in the family environment may have contributed to our results considering that the relationship between parental and adolescent pain may be a result of complex interactions between genetics, environmental factors and learned pain behavior [14–17]. Parent factors may shape adolescents’ pain development and pain management from both a resilience perspective and a risk perspective [16, 18, 19], and differences in adolescents’ attachment to their caregivers and how they communicate about pain might affect how adolescents experience and manage pain [81].
We found that about half of adolescents and parents reported intake of OTC analgesics and that parents reported more frequent intake compared to the adolescents. Considering the relatively low intensity of pain reported, this might indicate that adolescents and parents use OTC analgesics for reasons other than only pain relief. According to Skarstein et al.’s [82] review, parents are the most important source of information regarding adolescents’ use of OTC analgesics, as well as the main supplier. Thus, our findings highlight that informing parents, adolescents, and society about how to use OTC analgesics appropriately should be a high priority.
Contrary to previous studies that have shown that children from families with low SES experience pain more frequently [2, 20, 21], we found that the three adolescent pain groups were similar concerning SES factors such as adult members of the household, parental work status, parental education level and household income. A possible explanation for this might be that our sample mainly consisted of adolescents from families with higher levels of SES. However, it is important to highlight that although significant shared effects between family members (e.g., economy, education, cohabitant status) is associated with chronic pain, most explanations for chronic pain are considered to be at the individual level [83].
Strengths and limitations
The main strengths of this study include the relatively large sample of adolescent–parent dyads recruited from a variety of schools and that the selected analyzed variables were assessed with well-validated instruments. The limitations of this study include the cross-sectional design, which makes causal inference challenging to determine. Further, our meditation analyses are of an exploratory nature and based on our assumptions and understanding of the current research area. Thus, we can assume the direction of the indirect and direct effects. Another limitation is linked to the low response rate. We do not have information about the nonparticipating adolescents and parents. Therefore, we cannot assess whether the nonparticipants and participants differed in any way. Also, we only included one of each adolescent’s parents, which may have affected the results. Hence, the inclusion of both parents is recommended in future studies. However, more than three quarters of the adolescents lived with both parents and had parents who were both working. Further, among the participating parents, around three quarters had higher education level, were working full time and had a household income of more than 750,000 NOK/year. This indicates that the results may not be representative of adolescents within families with lower SES, which should be considered when interpreting our results. Further, the pain intensity reported by the adolescents is not considered high, which indicates that the results may not be representative of adolescents with higher levels of pain. Moreover, sample size and heterogeneity in the sample may have led to self-efficacy not being significant in our mediation analyses. We can therefore not exclude a possible significant influence from self-efficacy even if we were not able to show it in our study. Thus, we recommend a larger sample in future studies.
Implications
This study contributes to more knowledge of factors that characterizes adolescents with and without pain in a school-based setting, which can help teachers, public health nurses, parents and researchers better understand the cause of pain problems and find the best strategies to help adolescents with pain. It seems nearly impossible to focus solely on singular factors when helping adolescents to cope with pain. Thus, we recommend an individual, holistic approach to adolescents’ pain. In order to have an increased focus on protective and resilience factors, we suggest that public health nurses include routine-questions about self-esteem and self-efficacy in their consultations with adolescents who experience pain. Moreover, considering that the current COVID-19 pandemic is associated with increased stress and loneliness in adolescents [84, 85] parents, teachers, health professionals and researchers should be aware of the risk for an increase in pain problems among adolescents during and after the pandemic.
Based on our results from the mediation analyses, we recommend that HRQOL-promoting interventions among adolescents with pain should focus on a strengthening of their self-esteem and self-efficacy. It is demanding to intervene on risk-factors associated with adolescents’ pain such as SES, stress, and parental factors. However, interventions aimed at increasing self-esteem and self-efficacy is promising and also possible to carry out, for instance in a school setting, and should thus be a high priority. Considering that the basis for self-esteem and self-efficacy is founded during childhood, we recommend that a strengthening of these resilience factors should be a focus in early age, not only when reaching adolescence. We suggest the school setting as an important arena for resilience-promoting interventions.
Conclusions
This cross-sectional study among 14–15-year-old adolescents demonstrates the complexity and subjectivity within adolescent pain and shows that adolescents with pain differ from adolescents without pain when it comes to gender and school absence and factors within-person (self-efficacy, self-esteem, stress, sleeping problems) and between-persons (loneliness). We found no statistically significant differences between the adolescent pain groups, considering the selected parental factors; however, more adolescents with persistent pain reported that someone in their family had pain. Our results emphasize that longer pain duration makes adolescents more vulnerable, especially considering peer relationship. Furthermore, the results of our mediation analyses confirm the importance of resilience factors for HRQOL in adolescents with persistent pain but indicate that self-esteem plays a more important role than self-efficacy. Still, to promote HRQOL in adolescents with persistent pain, we suggest a strengthening of both their self-esteem and self-efficacy. We highlight the need for an individual, holistic approach to adolescent pain.
Supplementary Information
Acknowledgements
We are grateful to all the adolescents and parents who participated in the study and all the teachers, school nurses and administrative school staff who made this study possible. We would also like to thank Hanne Hvidsten, Gunhild S. Øverbø and Anne Berit Rege for their valuable help.
Abbreviations
- BPI
Brief pain inventory
- GSE
General self-efficacy scale
- HRQOL
Health-related quality of life
- LPQ
Lübeck pain-screening questionnaire
- MCS
Mental component summary scale
- OTC
Over the counter
- PCS
Physical component summary scale
- PSQ
Perceived stress questionnaire
- RSES
Rosenberg self-esteem scale
- SES
Socioeconomic status
- RAND-36
The 36-item medical outcomes study short form
- ULS
UCLA loneliness scale
Authors' contributions
All authors contributed to the conception of the study and its design. HTM, along with SS and GR, was responsible for the recruitment. HTM and MCS performed the data analyses. HTM wrote the first draft of the manuscript, and all the authors (HTM, KH, SH, SS, MCS and GR) commented on previous versions of the manuscript. All the authors read and approved the final manuscript.
Funding
This study is part of the first author’s doctoral thesis at the University of Agder and was financially supported by the Norwegian Ministry of Education and Research.
Availability of data and materials
The datasets used and/or analyzed during the current study are not publicly available due to General Data Protection Regulation laws but are available from the corresponding author on reasonable request and with permission from the Norwegian Centre for Research Data.
Declarations
Ethics approval and consent to participate
The adolescents received oral and written information. The written information was distributed to the parents. Active informed consent was obtained from both the adolescents and their parents. Data in the study were anonymized. All procedures performed in the study were in accordance with the ethical standards of the institutional and/or national research committee, as well as with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. Approval was obtained from the ethics committee of the Faculty of Health and Sport Sciences at the University of Agder and from the Norwegian Centre for Research Data (NSD Reference: 60981).
Consent for publication
Not applicable.
Competing interests
The authors declare that they have no competing interests.
Footnotes
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
References
- 1.Swain MS, Henschke N, Kamper SJ, Gobina I, Ottová-Jordan V, Maher CG. An international survey of pain in adolescents. BMC Public Health. 2014;14:447. doi: 10.1186/1471-2458-14-447. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Du Y, Knopf H, Zhuang W, Ellert U. Pain perceived in a national community sample of German children and adolescents. Eur J Pain. 2011;15(6):649–657. doi: 10.1016/j.ejpain.2010.11.009. [DOI] [PubMed] [Google Scholar]
- 3.Haraldstad K, Christophersen KA, Helseth S. Health-related quality of life and pain in children and adolescents: a school survey. BMC Pediatr. 2017;17(1):174. doi: 10.1186/s12887-017-0927-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.McKillop HN, Banez GA. A broad consideration of risk factors in pediatric chronic pain: Where to go from here? Children (Basel) 2016;3(4):38. doi: 10.3390/children3040038. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Hassett AL, Hilliard PE, Goesling J, Clauw DJ, Harte SE, Brummett CM. Reports of chronic pain in childhood and adolescence among patients at a tertiary care pain clinic. J Pain. 2013;14(11):1390–1397. doi: 10.1016/j.jpain.2013.06.010. [DOI] [PubMed] [Google Scholar]
- 6.Batley S, Aartun E, Boyle E, Hartvigsen J, Stern PJ, Hestbæk L. The association between psychological and social factors and spinal pain in adolescents. Eur J Pediatr. 2019;178(3):275–286. doi: 10.1007/s00431-018-3291-y. [DOI] [PubMed] [Google Scholar]
- 7.Sørensen K, Christiansen B. Adolescents' experience of complex persistent pain. Scand J Pain. 2017;15:106–112. doi: 10.1016/j.sjpain.2017.02.002. [DOI] [PubMed] [Google Scholar]
- 8.Haraldstad K, Sorum R, Eide H, Natvig GK, Helseth S. Pain in children and adolescents: prevalence, impact on daily life, and parents' perception, a school survey. Scand J Caring Sci. 2011;25(1):27–36. doi: 10.1111/j.1471-6712.2010.00785.x. [DOI] [PubMed] [Google Scholar]
- 9.Forgeron PA, King S, Stinson JN, McGrath PJ, MacDonald AJ, Chambers CT. Social functioning and peer relationships in children and adolescents with chronic pain: a systematic review. Pain Res Manag. 2010;15(1):27–41. doi: 10.1155/2010/820407. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Ravens-Sieberer U, Erhart M, Wille N, Wetzel R, Nickel J, Bullinger M. Generic health-related quality-of-life assessment in children and adolescents: methodological considerations. Pharmacoeconomics. 2006;24(12):1199–1220. doi: 10.2165/00019053-200624120-00005. [DOI] [PubMed] [Google Scholar]
- 11.Helseth S, Haraldstad K, Kvarme LG, Reinertsen H, Skarstein S, Winger A. Smerte hos barn og unge [pain in children and adolescents] In: Helseth S, Leegaard M, Nortvedt F, editors. Livskvalitet og smerte: et mangfoldig forskningsfelt [quality of life and pain: a diverse field of research] Oslo: Gyldendal Akademisk; 2016. pp. 25–40. [Google Scholar]
- 12.Raja SN, Carr DB, Cohen M, Finnerup NB, Flor H, Gibson S, et al. The revised international association for the study of pain definition of pain: concepts, challenges, and compromises. Pain. 2020;161(9):1976–1982. doi: 10.1097/j.pain.0000000000001939. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Hjern A, Alfven G, Ostberg V. School stressors, psychological complaints and psychosomatic pain. Acta Paediatr. 2008;97(1):112–117. doi: 10.1111/j.1651-2227.2007.00585.x. [DOI] [PubMed] [Google Scholar]
- 14.Hoftun GB, Romundstad PR, Rygg M. Association of parental chronic pain with chronic pain in the adolescent and young adult: family linkage data from the HUNT study. JAMA Pediatr. 2013;167(1):61–69. doi: 10.1001/jamapediatrics.2013.422. [DOI] [PubMed] [Google Scholar]
- 15.Higgins KS, Birnie KA, Chambers CT, Wilson AC, Caes L, Clark AJ, et al. Offspring of parents with chronic pain: a systematic review and meta-analysis of pain, health, psychological, and family outcomes. Pain. 2015;156(11):2256–2266. doi: 10.1097/j.pain.0000000000000293. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Stone AL, Wilson AC. Transmission of risk from parents with chronic pain to offspring: an integrative conceptual model. Pain. 2016;157(12):2628–2639. doi: 10.1097/j.pain.0000000000000637. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Clementi MA, Faraji P, Poppert Cordts K, MacDougall K, Wilson A, Palermo TM, et al. Parent factors are associated with pain and activity limitations in youth with acute musculoskeletal pain: a cohort study. Clin J Pain. 2019;35(3):222–228. doi: 10.1097/AJP.0000000000000668. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Cousins LA, Kalapurakkel S, Cohen LL, Simons LE. Topical review: resilience resources and mechanisms in pediatric chronic pain. J Pediatr Psychol. 2015;40(9):840–845. doi: 10.1093/jpepsy/jsv037. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Palermo TM, Valrie CR, Karlson CW. Family and parent influences on pediatric chronic pain: a developmental perspective. Am Psychol. 2014;69(2):142–152. doi: 10.1037/a0035216. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Grøholt EK, Stigum H, Nordhagen R, Kohler L. Recurrent pain in children, socio-economic factors and accumulation in families. Eur J Epidemiol. 2003;18(10):965–975. doi: 10.1023/A:1025889912964. [DOI] [PubMed] [Google Scholar]
- 21.Myrtveit Saether SM, Sivertsen B, Haugland S, Boe T, Hysing M. Health complaints in late adolescence; frequency, factor structure and the association with socio-economic status. Scand J Public Health. 2018;46(1):141–149. doi: 10.1177/1403494817711359. [DOI] [PubMed] [Google Scholar]
- 22.Skrove M, Romundstad P, Indredavik MS. Chronic multisite pain in adolescent girls and boys with emotional and behavioral problems: the Young-HUNT study. Eur Child Adolesc Psychiatry. 2015;24(5):503–515. doi: 10.1007/s00787-014-0601-4. [DOI] [PubMed] [Google Scholar]
- 23.Wilson AC, Moss A, Palermo TM, Fales JL. Parent pain and catastrophizing are associated with pain, somatic symptoms, and pain-related disability among early adolescents. J Pediatr Psychol. 2014;39(4):418–426. doi: 10.1093/jpepsy/jst094. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Gobina I, Villberg J, Välimaa R, Tynjälä J, Whitehead R, Cosma A, et al. Prevalence of self-reported chronic pain among adolescents: evidence from 42 countries and regions. Eur J Pain. 2019;23(2):316–326. doi: 10.1002/ejp.1306. [DOI] [PubMed] [Google Scholar]
- 25.Treede R-D, Rief W, Barke A, Aziz Q, Bennett MI, Benoliel R, et al. A classification of chronic pain for ICD-11. Pain. 2015;156(6):1003–1007. doi: 10.1097/j.pain.0000000000000160. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26.Gaskin DJ, Richard P. The economic costs of pain in the United States. J Pain. 2012;13(8):715–724. doi: 10.1016/j.jpain.2012.03.009. [DOI] [PubMed] [Google Scholar]
- 27.Sleed M, Eccleston C, Beecham J, Knapp M, Jordan A. The economic impact of chronic pain in adolescence: methodological considerations and a preliminary costs-of-illness study. Pain. 2005;119(1–3):183–190. doi: 10.1016/j.pain.2005.09.028. [DOI] [PubMed] [Google Scholar]
- 28.Skarstein S, Bergem AK, Helseth S. How do mothers of adolescents with chronic pain experience their own quality of life? BMC Psychol. 2020;8(1):64. doi: 10.1186/s40359-020-00430-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.Kaasboll J, Ranoyen I, Nilsen W, Lydersen S, Indredavik MS. Associations between parental chronic pain and self-esteem, social competence, and family cohesion in adolescent girls and boys–family linkage data from the HUNT study. BMC Public Health. 2015;15:817. doi: 10.1186/s12889-015-2164-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Lee S, McMurtry CM, Summers C, Edwards K, Elik N, Lumley MN. Quality of life in youth with chronic pain: an examination of youth and parent resilience and risk factors. Clin J Pain. 2020;36(6):440–448. doi: 10.1097/AJP.0000000000000820. [DOI] [PubMed] [Google Scholar]
- 31.Rutter M. Implications of resilience concepts for scientific understanding. Ann N Y Acad Sci. 2006;1094:1–12. doi: 10.1196/annals.1376.002. [DOI] [PubMed] [Google Scholar]
- 32.Schwarzer R, Warner LM. Perceived self-efficacy and its relationship to resilience. In: Prince-Embury S, Saklofske DH, editors. Resilience in children, adolescents, and adults: translating research into practice. New York, NY: Springer; 2013. pp. 139–150. [Google Scholar]
- 33.Stewart DE, Yuen T. A systematic review of resilience in the physically ill. Psychosomatics. 2011;52(3):199–209. doi: 10.1016/j.psym.2011.01.036. [DOI] [PubMed] [Google Scholar]
- 34.Rosenberg M, Schooler C, Schoenbach C, Rosenberg F. Global self-esteem and specific self-esteem: different concepts, different outcomes. Am Socio Rev. 1995;60(1):141–156. doi: 10.2307/2096350. [DOI] [Google Scholar]
- 35.Freire T, Ferreira G. Health-related quality of life of adolescents: relations with positive and negative psychological dimensions. Int J Adolesc Youth. 2018;23(1):11–24. doi: 10.1080/02673843.2016.1262268. [DOI] [Google Scholar]
- 36.Otto C, Haller AC, Klasen F, Hölling H, Bullinger M, Ravens-Sieberer U. Risk and protective factors of health-related quality of life in children and adolescents: results of the longitudinal BELLA study. PLoS ONE. 2017;12(12):e0190363. doi: 10.1371/journal.pone.0190363. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 37.Gomes AC, Rebelo MA, de Queiroz AC, de Queiroz Herkrath AP, Herkrath FJ, Rebelo Vieira JM, et al. Socioeconomic status, social support, oral health beliefs, psychosocial factors, health behaviours and health-related quality of life in adolescents. Qual Life Res. 2020;29(1):141–151. doi: 10.1007/s11136-019-02279-6. [DOI] [PubMed] [Google Scholar]
- 38.Grasaas E, Helseth S, Fegran L, Stinson J, Smastuen M, Haraldstad K. Health-related quality of life in adolescents with persistent pain and the mediating role of self-efficacy: a cross-sectional study. Health Qual Life Outcomes. 2020;18(1):19. doi: 10.1186/s12955-020-1273-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 39.Haraldstad K, Kvarme LG, Christophersen K-A, Helseth S. Associations between self-efficacy, bullying and health-related quality of life in a school sample of adolescents: a cross-sectional study. BMC Public Health. 2019;19(1):757. doi: 10.1186/s12889-019-7115-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40.Kvarme LG, Haraldstad K, Helseth S, Sorum R, Natvig GK. Associations between general self-efficacy and health-related quality of life among 12–13-year-old school children: a cross-sectional survey. Health Qual Life Outcomes. 2009;7:85. doi: 10.1186/1477-7525-7-85. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41.Kalapurakkel S, Carpino EA, Lebel A, Simons LE. "Pain can't stop me": examining pain self-efficacy and acceptance as resilience processes among youth with chronic headache. J Pediatr Psychol. 2015;40(9):926–933. doi: 10.1093/jpepsy/jsu091. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Piko BF, Varga S, Mellor D. Are adolescents with high self-esteem protected from psychosomatic symptomatology? Eur J Pediatr. 2016;175(6):785–792. doi: 10.1007/s00431-016-2709-7. [DOI] [PubMed] [Google Scholar]
- 43.Mikkelsen HT, Haraldstad K, Helseth S, Skarstein S, Småstuen MC, Rohde G. Health-related quality of life is strongly associated with self-efficacy, self-esteem, loneliness, and stress in 14–15-year-old adolescents: a cross-sectional study. Health Qual Life Outcomes. 2020;18(1):352. doi: 10.1186/s12955-020-01585-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 44.Varni JW, Rapoff MA, Waldron SA, Gragg RA, Bernstein BH, Lindsley CB. Effects of perceived stress on pediatric chronic pain. J Behav Med. 1996;19(6):515–528. doi: 10.1007/BF01904901. [DOI] [PubMed] [Google Scholar]
- 45.Sawyer MG, Carbone JA, Whitham JN, Roberton DM, Taplin JE, Varni JW, et al. The relationship between health-related quality of life, pain, and coping strategies in juvenile arthritis–a one year prospective study. Qual Life Res. 2005;14(6):1585–1598. doi: 10.1007/s11136-004-7710-3. [DOI] [PubMed] [Google Scholar]
- 46.University of Oslo. Services for sensitive data (TSD) [Internet]. UiO: Oslo; 2020. [cited 2020 Mon 08] Available from: https://www.uio.no/english/services/it/research/sensitive-data/index.html.
- 47.Cleeland CS, Ryan KM. Pain assessment: global use of the brief pain inventory. Ann Acad Med Singap. 1994;23(2):129–138. [PubMed] [Google Scholar]
- 48.Klepstad P, Loge JH, Borchgrevink PC, Mendoza TR, Cleeland CS, Kaasa S. The Norwegian brief pain inventory questionnaire: translation and validation in cancer pain patients. J Pain Symptom Manag. 2002;24(5):517–525. doi: 10.1016/S0885-3924(02)00526-2. [DOI] [PubMed] [Google Scholar]
- 49.Winger A, Kvarstein G, Wyller VB, Sulheim D, Fagermoen E, Smastuen MC, et al. Pain and pressure pain thresholds in adolescents with chronic fatigue syndrome and healthy controls: a cross-sectional study. BMJ Open. 2014;4(9):e005920. doi: 10.1136/bmjopen-2014-005920. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 50.Roth-Isigkeit A, Thyen U, Stöven H, Schwarzenberger J, Schmucker P. Pain among children and adolescents: restrictions in daily living and triggering factors. Pediatrics. 2005;115(2):e152–e162. doi: 10.1542/peds.2004-0682. [DOI] [PubMed] [Google Scholar]
- 51.Skarstein S, Rosvold EO, Helseth S, Kvarme LG, Holager T, Smastuen MC, et al. High-frequency use of over-the-counter analgesics among adolescents: reflections of an emerging difficult life, a cross-sectional study. Scand J Caring Sci. 2014;28(1):49–56. doi: 10.1111/scs.12039. [DOI] [PubMed] [Google Scholar]
- 52.Lagerløv P, Holager T, Helseth S, Rosvold EO. Self-medication with over-the-counter analgesics among 15–16 year-old teenagers. Tidsskr Nor Laegeforen. 2009;129(15):1447–1450. doi: 10.4045/tidsskr.09.32759. [DOI] [PubMed] [Google Scholar]
- 53.Ravens-Sieberer U, Auquier P, Erhart M, Gosch A, Rajmil L, Bruil J, et al. The KIDSCREEN-27 quality of life measure for children and adolescents: psychometric results from a cross-cultural survey in 13 European countries. Qual Life Res. 2007;16(8):1347–1356. doi: 10.1007/s11136-007-9240-2. [DOI] [PubMed] [Google Scholar]
- 54.Andersen JR, Natvig GK, Haraldstad K, Skrede T, Aadland E, Resaland GK. Psychometric properties of the Norwegian version of the Kidscreen-27 questionnaire. Health Qual Life Outcomes. 2016;14:58. doi: 10.1186/s12955-016-0460-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 55.Ravens-Sieberer U, Gosch A. The Kidscreen questionnaires: quality of life questionnaires for children and adolescents; handbook. Lengerich: Pabst; 2006. [Google Scholar]
- 56.Robitail S, Ravens-Sieberer U, Simeoni MC, Rajmil L, Bruil J, Power M, et al. Testing the structural and cross-cultural validity of the KIDSCREEN-27 quality of life questionnaire. Qual Life Res. 2007;16(8):1335–1345. doi: 10.1007/s11136-007-9241-1. [DOI] [PubMed] [Google Scholar]
- 57.Ware JE, Jr, Sherbourne CD. The MOS 36-item short-form health survey (SF-36). I. Conceptual framework and item selection. Med Care. 1992;30(6):473–483. doi: 10.1097/00005650-199206000-00002. [DOI] [PubMed] [Google Scholar]
- 58.Ware JE, Kosinski M. SF-36 physical & mental health summary scales: a manual for users of version 1. Lincoln: Quality Metric; 2001. [Google Scholar]
- 59.Luszczynska A, Scholz U, Schwarzer R. The general self-efficacy scale: multicultural validation studies. J Psychol. 2005;139(5):439–457. doi: 10.3200/JRLP.139.5.439-457. [DOI] [PubMed] [Google Scholar]
- 60.Bonsaksen T, Lerdal A, Heir T, Ekeberg O, Skogstad L, Grimholt TK, et al. General self-efficacy in the Norwegian population: differences and similarities between sociodemographic groups. Scand J Public Health. 2019;47(7):695–704. doi: 10.1177/1403494818756701. [DOI] [PubMed] [Google Scholar]
- 61.Rosenberg M. Society and the adolescent self-image. Princeton: Princeton University Press; 1965. [Google Scholar]
- 62.Tambs K, Røysamb E. Selection of questions to short-form versions of original psychometric instruments in MoBa. Norsk Epidemiol. 2014;24(1–2):195–201. [Google Scholar]
- 63.Stensland S, Thoresen S, Wentzel-Larsen T, Dyb G. Interpersonal violence and overweight in adolescents: the HUNT study. Scand J Public Health. 2015;43(1):18–26. doi: 10.1177/1403494814556176. [DOI] [PubMed] [Google Scholar]
- 64.Guddal MH, Stensland SØ, Småstuen MC, Johnsen MB, Zwart J-A, Storheim K. Physical activity and sport participation among adolescents: associations with mental health in different age groups Results from the Young-HUNT study: a cross-sectional survey. BMJ Open. 2019;9(9):e028555. doi: 10.1136/bmjopen-2018-028555. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 65.Ranøyen I, Stenseng F, Klöckner CA, Wallander J, Jozefiak T. Familial aggregation of anxiety and depression in the community: the role of adolescents’ self-esteem and physical activity level (the HUNT Study) BMC Public Health. 2015;15(1):78. doi: 10.1186/s12889-015-1431-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 66.Yildiz MA, Duy B. Adaptation of the short-form of the UCLA Loneliness Scale (ULS-8) to Turkish for the adolescents. Düşünen Adam. 2014;27(3):194–203. doi: 10.5350/DAJPN2014270302. [DOI] [Google Scholar]
- 67.Hays RD, DiMatteo MR. A short-form measure of loneliness. J Pers Assess. 1987;51(1):69–81. doi: 10.1207/s15327752jpa5101_6. [DOI] [PubMed] [Google Scholar]
- 68.Wilson D, Cutts J, Lees I, Mapungwana S, Maunganidze L. Psychometric properties of the revised UCLA Loneliness Scale and two short-form measures of loneliness in Zimbabwe. J Pers Assess. 1992;59(1):72–81. doi: 10.1207/s15327752jpa5901_7. [DOI] [PubMed] [Google Scholar]
- 69.Levenstein S, Prantera C, Varvo V, Scribano ML, Berto E, Luzi C, et al. Development of the perceived stress questionnaire: a new tool for psychosomatic research. J Psychosom Res. 1993;37(1):19–32. doi: 10.1016/0022-3999(93)90120-5. [DOI] [PubMed] [Google Scholar]
- 70.Kocalevent RD, Levenstein S, Fliege H, Schmid G, Hinz A, Brähler E, et al. Contribution to the construct validity of the perceived stress questionnaire from a population-based survey. J Psychosom Res. 2007;63(1):71–81. doi: 10.1016/j.jpsychores.2007.02.010. [DOI] [PubMed] [Google Scholar]
- 71.Østerås B, Sigmundsson H, Haga M. Psychometric properties of the perceived stress questionnaire (PSQ) in 15–16 years old Norwegian adolescents. Front Psychol. 2018;9:1850. doi: 10.3389/fpsyg.2018.01850. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 72.Wolfson AR, Carskadon MA. Sleep schedules and daytime functioning in adolescents. Child Dev. 1998;69(4):875–887. doi: 10.1111/j.1467-8624.1998.tb06149.x. [DOI] [PubMed] [Google Scholar]
- 73.Wolfson AR, Carskadon MA, Acebo C, Seifer R, Fallone G, Labyak SE, et al. Evidence for the validity of a sleep habits survey for adolescents. Sleep. 2003;26(2):213–216. doi: 10.1093/sleep/26.2.213. [DOI] [PubMed] [Google Scholar]
- 74.Pallesen S, Saxvig IW, Molde H, Sørensen E, Wilhelmsen-Langeland A, Bjorvatn B. Brief report: behaviorally induced insufficient sleep syndrome in older adolescents: prevalence and correlates. J Adolesc. 2011;34(2):391–395. doi: 10.1016/j.adolescence.2010.02.005. [DOI] [PubMed] [Google Scholar]
- 75.Pallant J. SPSS survival manual: a step by step guide to data analysis using IBM SPSS. 6. Maidenhead: McGraw Hill Education; 2016. [Google Scholar]
- 76.Hayes AF. Introduction to mediation, moderation, and conditional process analysis: a regression-based approach. 2. New York: The Guilford Press; 2018. [Google Scholar]
- 77.Preacher KJ, Hayes AF. SPSS and SAS procedures for estimating indirect effects in simple mediation models. Behav Res Methods Instrum Comput. 2004;36(4):717–731. doi: 10.3758/BF03206553. [DOI] [PubMed] [Google Scholar]
- 78.Vanhalst J, Luyckx K, Scholte RHJ, Engels RCME, Goossens L. Low Self-Esteem as a risk factor for loneliness in adolescence: perceived—but not actual—social acceptance as an underlying mechanism. J Abnorm Child Psychol. 2013;41(7):1067–1081. doi: 10.1007/s10802-013-9751-y. [DOI] [PubMed] [Google Scholar]
- 79.Helseth S, Misvaer N. Adolescents' perceptions of quality of life: what it is and what matters. J Clin Nurs. 2010;19(9–10):1454–1461. doi: 10.1111/j.1365-2702.2009.03069.x. [DOI] [PubMed] [Google Scholar]
- 80.Sawyer SM, Afifi RA, Bearinger LH, Blakemore SJ, Dick B, Ezeh AC, et al. Adolescence: a foundation for future health. Lancet. 2012;379(9826):1630–1640. doi: 10.1016/S0140-6736(12)60072-5. [DOI] [PubMed] [Google Scholar]
- 81.Lagerløv P, Rosvold EO, Holager T, Helseth S. How adolescents experience and cope with pain in daily life: a qualitative study on ways to cope and the use of over-the-counter analgesics. BMJ Open. 2016;6(3):e010184. doi: 10.1136/bmjopen-2015-010184. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 82.Skarstein S, Lagerløv P, Helseth S, Leegaard M. How do parents influence their adolescents' use of over-the-counter analgesics: a review of the current literature. J Clin Nurs. 2019;28(9–10):1451–1464. doi: 10.1111/jocn.14801. [DOI] [PubMed] [Google Scholar]
- 83.Campbell P, Jordan KP, Smith BH, Scotland G, Dunn KM. Chronic pain in families: a cross-sectional study of shared social, behavioural, and environmental influences. Pain. 2018;159(1):41–47. doi: 10.1097/j.pain.0000000000001062. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 84.Loades ME, Chatburn E, Higson-Sweeney N, Reynolds S, Shafran R, Brigden A, et al. Rapid systematic review: the impact of social isolation and loneliness on the mental health of children and adolescents in the context of COVID-19. J Am Acad Child Adolesc Psychiatry. 2020;59(11):1218–39.e3. doi: 10.1016/j.jaac.2020.05.009. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 85.Fegert JM, Vitiello B, Plener PL, Clemens V. Challenges and burden of the Coronavirus 2019 (COVID-19) pandemic for child and adolescent mental health: a narrative review to highlight clinical and research needs in the acute phase and the long return to normality. Child Adolesc Psychiatry Ment Health. 2020;14:20. doi: 10.1186/s13034-020-00329-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Data Availability Statement
The datasets used and/or analyzed during the current study are not publicly available due to General Data Protection Regulation laws but are available from the corresponding author on reasonable request and with permission from the Norwegian Centre for Research Data.