|Year : 2020 | Volume
| Issue : 1 | Page : 55-63
Intervention Protocol: Technology-Based Psychosocial Motivation for Children with Cancer and Their Parents: A Randomized Trial
Zeynep Kisecik Sengul1, Ebru Kilicarslan Toruner2
1 Department of Nursing, Health Sciences Faculty, Kirikkale University, Kirikkale, Turkey
2 Department of Nursing, Health Sciences Faculty, Gazi University Ankara, Ankara, Turkey
|Date of Submission||22-Nov-2018|
|Date of Acceptance||09-Apr-2019|
|Date of Web Publication||24-Jun-2019|
Zeynep Kisecik Sengul
Department of Nursing, Health Sciences Faculty, Kirikkale University, Kirikkale
Source of Support: None, Conflict of Interest: None
Objective: This experimental randomized controlled trial will be to examine the impact of a technology-based psychosocial motivation program on children and families who are being followed up on a diagnosis of cancer. Methods: The research is based on the “Transactional Model of Stress and Coping.” This study will be conducted on children with leukemia, aged 9–18 years, and their parents, who will be followed in the consolidation treatment phase in the hematology wards and outpatient clinic of a university hospital. Data collection will consist of the children's and parents' descriptive characteristic form, the Spielberger State Anxiety Inventory for Parents, the State-Trait Anxiety Inventory for Children, the Pediatric Cancer Coping Scale, the Pediatric Quality of Life Inventory, and process evaluation forms. A 10-week program will be implemented for the children in the intervention group through web-based training, coaching interviews and counseling via video mobile calls, mobile messages and children's stories, progressive muscle relaxation and breathing exercises, and imagination interventions. During the same period, parents will also receive web-based training, coaching sessions, counseling, mobile messages, and progressive muscle relaxation exercises. Results: It is thought that after the intervention the stress level of the child and the family will decrease, the coping skills of the children will improve, and their quality of life will increase. Conclusions: It is thought that the treatment process can be affected positively by providing psychosocial support to children and their families who receive cancer treatment.
Keywords: Cancer, child, motivation, parent, program, psychosocial, technology
|How to cite this article:|
Sengul ZK, Toruner EK. Intervention Protocol: Technology-Based Psychosocial Motivation for Children with Cancer and Their Parents: A Randomized Trial. Asia Pac J Oncol Nurs 2020;7:55-63
|How to cite this URL:|
Sengul ZK, Toruner EK. Intervention Protocol: Technology-Based Psychosocial Motivation for Children with Cancer and Their Parents: A Randomized Trial. Asia Pac J Oncol Nurs [serial online] 2020 [cited 2020 Mar 28];7:55-63. Available from: http://www.apjon.org/text.asp?2020/7/1/55/260883
| Introduction|| |
The overall incidence rate of childhood cancer ranges from 50 to 200 million worldwide. The number of children who are diagnosed with cancer is increasing, and the life expectancy of children with cancer is being prolonged with improved diagnosis and treatment methods. The increase in the number of children with cancer has led to a corresponding increase in psychosocial needs among children and their families.
In this process, children are often concerned about their illness, feeling sad and isolated. Children and adolescents may feel challenged and experience a deterioration in body image, a loss of independence, inability to plan for the future, a decrease in concentration and attendance, a decrease in cognitive abilities, impairment of daily routines, limitations in activity, difficulties with respect to peer relations, peer bullying, and ridicule.,,, The quality of life of children who are affected by psychosocial problems and have to cope with many stressful situations is also diminishing., It is for this reason that the development of psychosocial programs to support children is gaining more and more importance.
Cancer treatment affects families as well as children, both physically and psychosocially., After a diagnosis of cancer, families experience difficulties due to uncertainties about the future, the disappearance of normal family life, issues related to siblings, and financial problems, all of which lead to a deterioration of physical and psychosocial health. From a social perspective, the long treatment process increases the health costs of countries, creating an economic burden.
Treatment for children with cancer has usually been focused on physical interventions, whereas psychosocial interventions have remained limited. There are some programs in literature that aim to improve psychosocial aspects in the case of children with chronic illnesses. These programs seem to have been aimed at patients with diseases such as cancer, asthma, and diabetes.,, They include coping skills, cognitive behavioral approaches involving relaxation exercises,, group-based therapeutic exercise programs, yoga, guided imagery, hypnotic relaxation, meditation, physical exercise, and relaxation exercises. As a result of these programs, it was determined that children's anxiety levels had decreased, their sleep quality had increased, and their quality of life, self-efficacy, and coping skills had improved.,,,,, There are also programs for parents of children with chronic illnesses that include dimensions such as cognitive behavioral approaches, family therapy, and problem-solving therapy.
A psychosocial health-promoting program with multiple dimensions for children with cancer and their parents was not detected in literature. In the context of holistic care, there is a need for programs that improve the psychosocial health of children and families who are being followed up because of a cancer diagnosis. It is thought that these programs will enhance nursing care by decreasing stress, improving coping skills, and increasing the quality of life of both the child and the family. For instance, a number of psychosocial problems are likely to be encountered during the treatment process of children diagnosed with leukemia, which may affect their healing process. This study was aimed at providing psychosocial support to children with leukemia and their families. Today, the use of technology has become widespread in all areas. Thus, there have been effective initiatives to apply technology to the field of health, especially in diagnosis, treatment, and follow-up process of the disease, as individuals have started to receive health services online in their homes. In this study, technology-based programs were employed to ensure the continuation of health-care services and ease of communication. This article reveals the content and implementation plan of a psychosocial motivation program built for children diagnosed with leukemia and their families. The results of the study will be disseminated when the application has been completed.
Aims and hypotheses
This research was planned in an effort to examine the impact of a 10-week technology-based psychosocial motivation program for children with cancer and their parents.
Specific hypotheses include the following:
- H0– There is no meaningful difference between the coping skills, stress levels, and quality of life of children who have received psychosocial motivation programs and those of children who have not
- H1– The stress levels of children exposed to a motivational program are lower than those of children in the control group
- H2– The coping skills of children exposed to a motivation program are higher than those of children in the control group
- H3– The quality of life of children exposed to a motivation program is higher than that of children in the control group
- H4– The stress level of parents in the intervention group is lower than that of parents in the control group.
| Methods|| |
This pilot study was planned to be of a randomized controlled experimental research design. The research was carried out from January 3 to 9, 2019, in the hematology outpatient clinic and wards of a university hospital in Turkey's Central Anatolia. The universe of the study will be children with leukemia aged 9–18 years receiving treatment in the hematology wards or outpatient clinic of a university hospital and their parents. To avoid any bias, children will be paired prior to randomization based on their age and sex. The children will be allocated to the intervention or control groups using the simple random method, which will be conducted by an individual blinded to the research. The inclusion criteria for the children are as follows: (a) receiving treatment at the consolidation phase, (b) diagnosed with leukemia, (c) Turkish speaking, (d) between the ages of 9 and 18, (e) having Internet access on a smartphone or computer, (f) agreeing to participate together with a parent, (g) and ability to participate in the program for 8 weeks. The inclusion criteria for the parents are as follows: (a) Turkish speaking, (b) Internet access on a smartphone or computer, (c) agreeing to participate in the study, and (d) ability to participate in the program for 8 weeks. The exclusion criteria for the study are as follows: (a) having experienced an important life event in the past 6 months (death, divorce, etc.), (b) having another important disease that can increase stress and suppress coping skills in the family, (c) wishing to leave the study, and (d) inability to continue the program for more than 1 week.
Children under 18 years who are diagnosed with leukemia are followed up in a hematology ward or outpatient clinic. Patients with leukemia are tracked in clinics during the diagnosis, treatment, and control stages.
Data collection tools
In this study, the children and their parents will complete the Children's and Parents' Descriptive Characteristics Form and process evaluation forms. In addition, the children will fill out the State-Trait Anxiety Inventory for Children, Pediatric Cancer Coping Scale, and Pediatric Quality of Life Inventory. Parents will complete the Spielberger State Anxiety Inventory.
Children's and Parents' Descriptive Characteristics Form
The descriptive characteristics form was developed by the researchers in light of the literature.,,, There are seven close-ended questions about the children's age, education, and treatment status and six close-ended questions about the parents' age, education, and working status.
Spielberger State Anxiety Inventory
This scale was developed by Spielberger et al. for the purpose of determining the anxiety levels of individuals aged 14 and over. The Turkish validity and reliability of the scale was assessed by Öner and Le Compte. The State Anxiety Inventory will be used in our study. The scores on the scale range from 20 to 80, and the higher the score, the higher the level of anxiety. The original Cronbach's alpha value ranged from 0.86 to 0.95. Cronbach's alpha values in the Turkish form ranged from 0.94 to 0.96 on the State Anxiety Scale.
State-Trait Anxiety Inventory for Children
This scale was developed by Spielberger to measure the level of anxiety in children. The validity of the Turkish version was assessed by Özusta on children aged 9–12 years. Cronbach's alpha values ranged from 0.78 to 0.81 on the original scale. The Cronbach's alpha values of the scale in the Turkish version were found to be 0.82 for the State Anxiety Scale and 0.81 for the Trait Anxiety Scale. The scale can be used in our country for children aged 9 and older. National and international studies had reported that the scale can be used for ages up to 17–18 years.,,,,,,, It is observed that the scale has been used in studies to determine the stress situations of children with cancer.,,
Pediatric Quality of Life Inventory (PedsQL™)
This scale was developed by Varni et al. to measure the quality of life of children and adolescents aged 2–18 years. The scale consists of 23 items and is scored from 0 to 100. The higher the score, the higher the quality of life. The original form's Cronbach's alpha value was 0.93. The validity and reliability studies for the Turkish version of the scale for 8–12 year olds were conducted by Cakın Memik et al., and the Turkish validity and reliability studies for 13–18 year olds were carried out by Cakın Memik et al. The Cronbach's alpha coefficient was found to be 0.82 in the adolescents' form and 0.86 in the children's form., The scale has been used in studies to determine the quality of life of children with cancer.,
Pediatric Cancer Coping Scale
This scale was developed by Wu et al. for children with cancer between the ages of 7 and 18 years. The scale comprises 33 items related to cognitive coping, problem-oriented coping, and defensive coping. The items are measured on a scale of 0 (never) to 3 (always). Higher scores on the scale indicate a high level of coping strategies. Cronbach's alpha coefficient in the original study was 0.91. The Turkish validity reliability study of the scale was initiated by the researchers.
Process evaluation forms
The following six forms developed by the researchers will be used to evaluate the process of the study:
- Website training follow-up form – Completion status of training modules, problems experienced during the follow-up of modules, and frequently asked questions will be tracked with this form
- Mobile video interview follow-up form – Interview dates, time, contents, and questions will be recorded on this form
- Counseling follow-up form – The reason for the counseling request, the time, and the results will be recorded on this form
- Children's follow-up form for interventions – Interventions such as progressive muscle relaxation, breathing exercises, imagination, story reading and writing, and the awareness wheel will be monitored weekly and related problems will be recorded on this form
- Parents' follow-up form for interventions – Progressive muscle relaxation, breathing exercises, parents' approach to the child, and the problems experienced will be recorded on this form
- Satisfaction and suggestion form – This is a feedback form for the program to be given to the children and their parents at the end of the intervention.
When we look at the studies in which the coping strategies of children with cancer have been examined, it can be seen that Lazarus and Folkman's “Transactional Model of Stress and Coping” has been most commonly used.,,, According to this model, an individual employs coping strategies that are problem focused or emotion focused when faced with a stressful situation. Interventions in the study were planned using the Transactional Model of Stress and Coping [Table 1].
|Table 1: Use of transactional stress and coping model within motivation program|
Click here to view
A preliminary application of the data collection forms and the technology-based program will be administered to five children between the ages of 9 and 18 years with a diagnosis of leukemia and their parents. After the preliminary application, changes and corrections will be applied to the forms and program if necessary.
Technology-based psychosocial motivational program interventions
A 10-week program involving web-based training, mobile video coaching interviews and counseling, mobile messages and children's story reading and writing, progressive muscle relaxation and breathing exercises, and imagination interventions will be implemented on the children in the intervention group. The flowchart of the study is shown in [Figure 1]. The interventions for children and parents are shown in [Figure 2]. The research forms for the children and their families in the intervention group will be implemented at the beginning and end of the program.
|Figure 2: Interventions to be applied to children and their parents in the technology-based psychosocial motivation program|
Click here to view
In the first 2 weeks of the program for children, four training modules will be presented via a web-based training site [Table 2]. The application of modules 1 and 2 of the training on the website will be carried out in the 1st week of the research, and the implementation of modules 3 and 4 will be done in the 2nd week.
|Table 2: Motivation program modules and contents for children on website|
Click here to view
Parents of the children in the intervention group will also be exposed to two training modules for relaxation and communication with children through the website [Table 3]. Once the website modules have been developed by the researchers, experts will be consulted for content validity to assess the appropriateness of the content for children and parents.
Mobile video coaching interviews and counseling
A mobile face-to-face coaching interview with the children will be conducted once a week for 45–60 min. There will be a total of nine coaching interviews in the program. The researchers will offer parents two mobile online video interviews and 24/7 telephone counseling services for both children and families.
Progressive muscle relaxation, breathing exercises, and imagination
The videos of relaxation exercises containing progressive muscle relaxation exercises prepared by the Turkish Psychological Association will be shown in the second module. The training module will feature imagination videos of the sky accompanied by the sound of a rhythmic drum to be prepared by the researchers, as well as imagination videos of purification from emotional burdens, along with water sounds and a voice accompaniment.
Children will be asked to perform a progressive muscle relaxation technique (one application/day) and breathing (three breaths/day) for at least 3 days/week for 9 weeks. Following the completion of module 3 in the 2nd week, an imaging technique will be added to the muscle relaxation and breathing exercises. Parents will be asked to perform muscle relaxation and breathing exercises for 8 weeks after completing the training modules.
Messages via mobile
Three separate messages will be sent to the children's mobile phones every week. The first message's content will be motivation messages. The second type of message content will be a reminder to do the muscle relaxation, breathing, and imagination exercises. The third type of message will be a therapeutic children's story. To help the child manage his/her perception in a positive way, eight therapeutic stories selected by the researchers will be prepared as an animated video and sent to the child's phone. At the end of the program, the child will be asked to write a personal narrative about the importance of perception.
Routine practices in the control group of children and their families will continue. The data collection forms will be administered to the children and their parents at the beginning of the study. Except the descriptive characteristic form, the questionnaires will be readministered at the end of the program.
Permission has been obtained from the university's Ethics Committee (Approval No. 2018-368) and the hospital (No. 98206329/770). The informed written consent of children and parents agreeing to participate in the study will also be collected.
Data obtained in the study will be analyzed with the IBM SPSS for Windows Version 21.0 program, and the frequency values and percentage distributions will be calculated. The variables' compliance with normal distribution will be examined with visual (histogram and probability graphics) and analytical (Kolmogorov–Smirnov) methods. The Chi-square test or Fisher's exact test will be employed to compare the nominal data between the groups. For the comparison of the data in the two groups that have continuous variables (ordinal), the Mann–Whitney U-test will be used for nonnormally distributed data and the Student's t-test will be used for normally distributed data. On investigating the associations between nonnormally distributed and ordinal variables, the correlation coefficients and their significance will be calculated using the Spearman's test. The significance level was set at 0.05.
| Results|| |
After the motivation program, it is thought that the stress level of the child and the family will decrease, the coping skills of the children will improve, and the quality of life will increase.
| Discussion|| |
With the advancement of technology, children and their parents can access the Internet easily and use web pages as a source of information. Considering that children and their parents can reach reliable information and find answers to problems encountered during the treatment process via the Internet, and that the maintenance of care can be ensured by means of the Internet providing the dissemination of scientific knowledge, a web-based motivation program was planned to be conducted in the study. There is a need for separate modules for children and their parents in the organization of programs. Meanwhile, it is necessary to prepare program contents which could appeal to children of different ages and their parents, to make content analysis, and to take expert views on the content. The challenges of the program include children's participation in relaxation exercises, imagination and coaching interviews within program contents, and staying online continuously during interviews via Whatsapp. The obstacles against the implementation of the program include failure to carry out the program due to lack of internet access by the children and their parents, difficulty in reaching the sample group in the clinics, insufficient area allocated for the introduction of the program in the hospital, and the difficulty of children and their parents for spending 60 min to participate in the program.
In this study, a combination of various methods will be employed for both children and parents. Considering that no similar study was encountered in literature, it is thought that this study will contribute to evidence-based information. With regard to the limitations of the study, the information obtained by the measurement tools is limited to the responses of the patients to the scale questionnaires. In addition, the research will be conducted at a single hospital. Hence, the results are likely to vary across individuals and cultures. Furthermore, the fact that only children and parents with internet access were included in the study may prove to be a limitation.
| Conclusion|| |
Supporting children and parents in the long and challenging process of cancer treatment plays a crucial role in maintaining compliance with treatment, increasing comfort, and dealing with stress. It is believed that a motivation program to be applied with family-centered care, cognitive behavioral methods and coaching techniques will contribute to helping children and parents control their emotional status and develop effective coping skills during the course of illness and through the treatment process.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
Kazak AE, Abrams AN, Banks J, Christofferson J, DiDonato S, Grootenhuis MA, et al.
Psychosocial assessment as a standard of care in pediatric cancer. Pediatr Blood Cancer 2015;62 Suppl 5:S426-59.
Enskär K, von Essen L. Physical problems and psychosocial function in children with cancer. Paediatr Nurs 2008;20:37-41.
Barakat LP, Galtieri LR, Szalda D, Schwartz LA. Assessing the psychosocial needs and program preferences of adolescents and young adults with cancer. Support Care Cancer 2016;24:823-32.
Li HC, Chung OK, Chiu SY. The impact of cancer on children's physical, emotional, and psychosocial well-being. Cancer Nurs 2010;33:47-54.
Hildenbrand AK, Clawson KJ, Alderfer MA, Marsac ML. Coping with pediatric cancer: Strategies employed by children and their parents to manage cancer-related stressors during treatment. J Pediatr Oncol Nurs 2011;28:344-54.
Patel SK, Schulte, F, Kelly NC, Steele AC. Neurocognitive late effects in children with cancer. In: Abrams AN, Muriel AC, Wiener L, editors. Pediatric Psychosocial Oncology: Textbook for Multidisciplinary Care. Switzerland: Springer International Publishing; 2016. p. 157-75.
Mitchell HR, Lu X, Myers RM, Sung L, Balsamo LM, Carroll WL, et al.
Prospective, longitudinal assessment of quality of life in children from diagnosis to 3 months off treatment for standard risk acute lymphoblastic leukemia: Results of children's oncology group study AALL0331. Int J Cancer 2016;138:332-9.
Pan HT, Wu LM, Wen SH. Quality of life and its predictors among children and adolescents with cancer. Cancer Nurs 2017;40:343-51.
McCarthy MC, McNeil R, Drew S, Dunt D, Kosola S, Orme L, et al.
Psychological distress and posttraumatic stress symptoms in adolescents and young adults with cancer and their parents. J Adolesc Young Adult Oncol 2016;5:322-9.
Klassen AF, Klaassen R, Dix D, Pritchard S, Yanofsky R, O'Donnell M, et al.
Impact of caring for a child with cancer on parents' health-related quality of life. J Clin Oncol 2008;26:5884-9.
Patterson JM, Holm KE, Gurney JG. The impact of childhood cancer on the family: A qualitative analysis of strains, resources, and coping behaviors. Psychooncology 2004;13:390-407.
Mariotto AB, Yabroff KR, Shao Y, Feuer EJ, Brown ML. Projections of the cost of cancer care in the United States: 2010-2020. J Natl Cancer Inst 2011;103:117-28.
van Dijk-Lokkart EM, Braam KI, Kaspers GJ, van Dulmen-den Broeder E, Takken T, Grootenhuis MA, et al.
Applicability and evaluation of a psychosocial intervention program for childhood cancer patients. Support Care Cancer 2015;23:2327-33.
Marriage D, Henderson J. Cognitive behaviour therapy for anxiety in children with asthma. Nurs Child Young People 2012;24:30-4.
Perfect MM, Elkins GR. Cognitive-behavioral therapy and hypnotic relaxation to treat sleep problems in an adolescent with diabetes. J Clin Psychol 2010;66:1205-15.
Grey M, Whittemore R, Jaser S, Ambrosino J, Lindemann E, Liberti L, et al.
Effects of coping skills training in school-age children with type 1 diabetes. Res Nurs Health 2009;32:405-18.
van Dijk-Lokkart EM, Braam KI, van Dulmen-den Broeder E, Kaspers GJ, Takken T, Grootenhuis MA, et al.
Effects of a combined physical and psychosocial intervention program for childhood cancer patients on quality of life and psychosocial functioning: Results of the QLIM randomized clinical trial. Psychooncology 2016;25:815-22.
Beulertz J, Prokop A, Rustler V, Bloch W, Felsch M, Baumann FT. Effects of a 6-month, group-based, therapeutic exercise program for childhood cancer outpatients on motor performance, level of activity, and quality of life. Pediatr Blood Cancer 2016;63:127-32.
Wurz A, Chamorro-Vina C, Guilcher GM, Schulte F, Culos-Reed SN. The feasibility and benefits of a 12-week yoga intervention for pediatric cancer out-patients. Pediatr Blood Cancer 2014;61:1828-34.
Malboeuf-Hurtubise C, Achille M, Muise L, Beauregard-Lacroix R, Vadnais M, Lacourse É. A mindfulness-based meditation pilot study: Lessons learned on acceptability and feasibility in adolescents with cancer. J Child Fam Stud 2016;25:1168-77.
Eccleston C, Palermo TM, Fisher E, Law E. Psychological interventions for parents of children and adolescents with chronic illness. Cochrane Database Syst Rev 2013;8:CD009660.
Wu LM, Chin CC, Chen CH, Lai FC, Tseng YY. Development and validation of the paediatric cancer coping scale. J Adv Nurs 2011;67:1142-51.
Li HC, Chung OK, Ho KY, Chiu SY, Lopez V. Coping strategies used by children hospitalized with cancer: An exploratory study. Psychooncology 2011;20:969-76.
Wu LM, Chiou SS, Sheen JM, Lin PC, Liao YM, Chen HM, et al.
Evaluating the acceptability and efficacy of a psycho-educational intervention for coping and symptom management by children with cancer: A randomized controlled study. J Adv Nurs 2014;70:1653-62.
Shosha GA, Abushaikha L, Marnocha S, Al Kalaldeh M. Perceived body image and coping in adolescents receiving chemotherapy: A phenomenological study. Int J Acad Res 2013;5:166-76.
Spielberger CD, Gorsuch RL, Lushene RE. Manual for the State-Trait Anxiety Inventory. Palo Alto, California: Consulting Psychologist Press; 1970.
Öner N, Le Compte A. State-Trait Anxiety İnventory Hand Book. 2nd
ed. İstanbul: Boǧaziçi University Press; 1985.
Spielberger CD, Russell JG, Crane RS. Assessment of anger: The State-Trait Anger Scale. In: Butcher JN, Spielberger CD, editors. Advances in Personality Assessment. Hillsdale, NJ: Erlbaum; 1983. p. 159-87.
Spielberger CD. Preliminary Test Manual for the State-Trait Anxiety Inventory for Children. Palo Alto, CA: Consulting Psychologists Press; 1973.
Özusta S. State–trait anxiety ınventory for children adaptation, validity and reliability study. Turk J Psychol 1995;10:32-44.
Toros F, Tot Ş, Düzovalı Ö. Depression and anxiety levels of parents and children with chronic illness. J Clin Psychiatry 2002;5:240-7.
Sabuncuoǧlu O, Çevikaslan A, Ve Berkem M. Depression, anxiety and behavior among adolescents in two affected areas after the Marmara Earthquake. J Clin Psychiatry 2003;6:189-97.
Özmen D, Özmen E, Çetinkaya A, Akil İÖ. Trait anger and anger expression styles in adolescents. Anatolian J Psychiatry 2016;17:65-73.
Nasıroǧlu S, Yolga Tahiroǧlu A, Avcı A, Gül Çelik G, Öztürk Z. Inpatient treatment of abused children and adolescents. Anatolian J Psychiatry 2012;13:285-91.
Shomaker LB, Bruggink S, Pivarunas B, Skoranski A, Foss J, Chaffin E, et al.
Pilot randomized controlled trial of a mindfulness-based group intervention in adolescent girls at risk for type 2 diabetes with depressive symptoms. Complement Ther Med 2017;32:66-74.
Grubenhoff JA, Currie D, Comstock RD, Juarez-Colunga E, Bajaj L, Kirkwood MW. Psychological factors associated with delayed symptom resolution in children with concussion. J Pediatr 2016;174:27-320.
Rabbitts JA, Groenewald CB, Tai GG, Palermo TM. Presurgical psychosocial predictors of acute postsurgical pain and quality of life in children undergoing major surgery. J Pain 2015;16:226-34.
Tsang TW, Kohn MR, Efron D, Clarke SD, Clark CR, Lamb C, et al.
Anxiety in young people with ADHD: Clinical and self-report outcomes. J Atten Disord 2015;19:18-26.
Altay N, Kilicarslan-Toruner E, Sari Ç. The effect of drawing and writing technique on the anxiety level of children undergoing cancer treatment. Eur J Oncol Nurs 2017;28:1-6.
Germann JN, Leonard D, Heath CL, Stewart SM, Leavey PJ. Hope as a predictor of anxiety and depressive symptoms following pediatric cancer diagnosis. J Pediatr Psychol 2018;43:152-61.
Fortier MA, Wahi A, Bruce C, Maurer EL, Stevenson R. Pain management at home in children with cancer: A daily diary study. Pediatr Blood Cancer 2014;61:1029-33.
Varni JW, Seid M, Rode CA. The pedsQL: Measurement model for the pediatric quality of life inventory. Med Care 1999;37:126-39.
Varni JW, Seid M, Kurtin PS. PedsQL 4.0: Reliability and validity of the pediatric quality of life inventory version 4.0 generic core scales in healthy and patient populations. Med Care 2001;39:800-12.
Cakın Memik N, Agaoglu B, Coskun A, Karakaya I. The validity and reliability of pediatric quality of life inventory in 8-12 year old Turkish children. Turk J Child Adolesc Ment Health 2008;15:87-98.
Cakin Memik N, Aǧaoǧlu B, Coşkun A, Uneri OS, Karakaya I. The validity and reliability of the Turkish pediatric quality of life inventory for children 13-18 years old. Turk Psikiyatri Derg 2007;18:353-63.
Ryerson AB, Wasilewski-Masker K, Border WL, Goodman M, Meacham L, Austin H, et al.
Pediatric quality of life in long-term survivors of childhood cancer treated with anthracyclines. Pediatr Blood Cancer 2016;63:2205-11.
Wettergren L, Kent EE, Mitchell SA, Zebrack B, Lynch CF, Rubenstein MB, et al.
Cancer negatively impacts on sexual function in adolescents and young adults: The AYA HOPE study. Psychooncology 2017;26:1632-9.
Shockey DP, Menzies V, Glick DF, Taylor AG, Boitnott A, Rovnyak V. Preprocedural distress in children with cancer: An intervention using biofeedback and relaxation. J Pediatr Oncol Nurs 2013;30:129-38.
Lazarus RS, Folkman S. Stress, Appraisal and Coping. New York: Springer Publisher; 1984.
Hayran M, Hayran M. Basic Statistics for Health Researchers. 1st
ed. Ankara: Art Offset Publishing and Organization; 2011.
| Authors|| |
Zeynep Kisecik Sengul
[Figure 1], [Figure 2]
[Table 1], [Table 2], [Table 3]