Design and Ethics
The study employed a two-arm, controlled trial design. Inclusion criteria for children were as follows: (1) should be between the ages of 3 and 8 years at the beginning of treatment, (2) should have a higher than average level of nighttime fears based on parental opinion, (3) should reach at least score five on a 10-point parent-reported visual-analogue scale (FOD), measuring the level of fear of the dark, (4) should not be involved in current treatment for nighttime fears or other internalizing problems, and (5) should be a native speaker of Hungarian. Thus, the basic criterion for inclusion was the subjective perception of the parent that the child was significantly afraid at nighttime. Contrary to previous efficacy studies, participation did not require a related clinical diagnosis.
Participating children were assigned to (1) a waitlist group; or (2) an intervention group that received 5-week parent-delivered bibliotherapy, using Uncle Lightfoot. Assignment was based on participants’ place of residence due to limited resources. (As recruitment and data collection was done solely by the first author, in-person meetings could only be carried out with families that were relatively easily accessible for her.) Variables were assessed at baseline, post-treatment and 20-week follow-up. The waitlist group received the self-help book after the follow-up measurement. The study received approval from the Hungarian United Ethical Review Committee for Research in Psychology (EPKEB) with the reference number 2017/62. Parents gave written informed consent and children gave assent to participate pre-treatment. Beyond the self-help book, participants received no compensation for their participation.
Procedure
The recruitment of the participants occurred between March 2017 and June 2018 in Hungary, through advertisements in preschools, general health practitioners’ offices and on social networking sites, as well as by contacting psychologists working in preschools. Interested parents made contact via e-mail or telephone, then completed a short online questionnaire that assessed whether they met the inclusion criteria.
Parents from the waitlist group completed the baseline, post-treatment and follow-up questionnaires online. With them, no in-person contact was made, which made it possible to involve families living to a considerable distance from the first author who did data collection. They were informed that the aim of the assessment is to capture the changes or stability of their child’s nighttime fears during a 20-week-period. With families from the intervention group, two in-person sessions were scheduled at pre-treatment and post-treatment, while they completed the follow-up questionnaire online. They were informed that the aim of the assessment is to measure the efficacy of Uncle Lightfoot. Enrollment and personal interviews were conducted by the first author who is a psychologist.
The intervention consisted of the use of the Hungarian translation of the revised version of the second edition of Uncle Lightfoot Flip that switch [28]. Uncle Lightfoot is a self-help book, suitable for parent-delivered therapy of nighttime fears. After the study of Lewis et al. [30], the book was supplemented with two more chapters. The book was translated into Hungarian by a clinical psychologist who was also a teacher of English as a second language.
Beyond the story of a young boy who overcomes his fear of the dark, it offers games (cognitive behavioral interventions) that are designed to help children overcome their own nighttime fears. The recommended games are mainly in vivo exposures, such as finding toys or playing in the dark. Other recommended activities include therapeutic-elaborative drawing and relaxation elements.
The intervention was carried out by parents at home. Information about how to use Uncle Lightfoot was provided at the pre-treatment in-person session, as well as by the written parental guide in the book. Parents were instructed to read the book or play the recommended games on each evening during the five weeks, and to complete the book at least one time over that period. Parents completed a daily log, tracking their intervention activity.
Participants
Figure 1 describes the flow of participants through the study. From the 155 interested parents and their child, 82 did not meet the inclusion criteria or chose not to participate after being informed in detail. Of the included 73 families, 63 participated in assessments at all three time points.
The final sample consisted of 33 children in the waitlist group and 30 in the intervention group. Sociodemographic characteristics are presented in Table 1. The gender distribution was to a marginally significant extent unequal in the two groups. In addition, due to the group assignment method, parents in the intervention group were capital city residents or lived in Pest county near the capital, had to a marginally significant extent higher education, and were significantly older than parents in the waitlist group. No other differences were observed among the sociodemographic characteristics of the two groups.
Table 1 Sociodemographic characteristics of the final sample by test groups
Measures
Child Interview
Children in the intervention group, with whom a personal meeting also took place, were asked to provide a rating of the level of their nighttime fear during the personal assessments at baseline and post-treatment. For that aim, a 3-point graphical assessment scale was used, which included faces, representing no fear, mild fear and severe fear.
Childhood Darkness Phobia Questionnaire (CDPQ) [34]
The CDPQ is a 5-item parent-report measure of children’s darkness or nighttime related fears of phobic intensity, including: (1) excessive fear triggered by nighttime or darkness, (2) the fear is persistent, occurring nearly every day, (3) the child avoids sleeping alone at nighttime in the dark, or endures it with anxiety, (4) the fear significantly impacts the child’s everyday life, and (5) the duration of fear lasts for several months. In such manner, the aspects taken into consideration by CDPQ, largely follow the DSM-5 (American Psychiatric Association [4]) criteria for specific phobia, although it does not require six months duration. Each item on the scale is answered on a 4-point scale (1 = Not at all to 4 = Absolutely). The total possible score on the CDPQ ranges from 5 to 20. A higher score indicates more pathological nighttime fears. The scale had acceptable internal consistency in the current study at post-treatment and follow up, while poor internal consistency at baseline (Cronbach’s Alphas [at baseline, post-treatment, follow-up, respectively] = 0.55, 0.72, 0.78).
What My Child Can Do At Night in the Dark (WICDAN-Parent Form) [35
]
The WICDAN is an 11-item parent-report measure of children’s nighttime behaviors and self-efficacy in dealing with their fear of the dark. Each item on the scale is answered on a 3-point scale (0 = No to 2 = Yes, easily). The total possible score on the WICDAN ranges from 0 to 22. A higher score indicates more adequate nighttime behavior. In the study of Lewis et al. [30] the mean score (SD) of the WICDAN was 7 (3.6) among children with nighttime fears at baseline, while 16.75 (3.9) post-treatment and 16.25 (4.5) at one-month follow up. WICDAN was translated into Hungarian using the back-translation method. First, three psychologists independently translated the scale into Hungarian, and then agreed on a consensual version. Second, a Hungarian psychologist, working in England made a back translation of this version. Finally, this back-translated version was then reviewed and compared with the original English version by the developer of the scale and by the first author. A consensus about the final translation was reached without any further major modifications. The Hungarian translation had good internal consistency in the current study at each assessment (Cronbach’s Alphas [at baseline, post-treatment, follow-up, respectively] = 0.86, 0.81, 0.88). The measurement also included a 10-point (1 = Not very afraid to 10 = Extremely afraid) fear of the dark assessment scale (FOD).
Separation Anxiety Avoidance Inventory - Parent Version (SAAI-P) [36]
SAAI-P is a 12-item parent-report scale that measures to what extent the child avoids different relevant situations. Each item on the scale is answered on a 5-point scale (0 = Never to 4 = Always). SAAI-P was translated into Hungarian using the back-translation method. Three psychologists independently translated it into Hungarian, and agreed on a consensual version. Then, a Hungarian psychologist, working in England made a back translation of this version. Finally, this back-translated version was compared with the original English version by the first author who found it to be accurate. Due to the previous experience regarding age-related items [36], a Not applicable response option was added in the current study and an average of responded items was calculated and used in further analysis. Hence the possible score of separation anxiety ranges from 0 to 4, and a higher score indicates more frequent separation anxiety symptoms. The Hungarian version of the scale had good internal consistency in the current study at each assessment (Cronbach’s Alphas [at baseline, post-treatment, follow-up, respectively] = 0.83, 0.81, 0.81).
Intervention Log
Parents in the intervention group completed a daily report during the 5-week intervention, about: (1) the use of the book on the previous day (yes/no), (2) the duration of reading the book (in minutes), (3) the duration of playing games offered by the book (in minutes), (4) games applied and (5) difficulties experienced (if yes, please describe).
Treatment Evaluation
As part of the post-treatment assessment, parents in the intervention group evaluated the intervention, partly based on the Treatment Evaluation Survey for Uncle Lightfoot, Flip That Switch-Revised, developed by Coffman [37]. Information was collected regarding the (1) number of times the complete book was read to the child, (2) use of any reward or reinforcement, (3) use of the parent’s guide, (4) perceived effectiveness of the book and related satisfaction, (5) how much the child enjoyed Uncle Lightfoot in comparison to other books on a 5-point scale (1 = Not really to 5 = Very much). At follow-up, further use of Uncle Lightfoot after post-treatment assessment was reported.
Data Analysis
Statistical analyses were performed using IBM SPSS Statistics 22 and criterion for statistical significances was set at the level of 5% (p < .05). Descriptive analyses are presented as proportions, means and standard deviations. For the continuous variables, comparisons were made through t-tests for independent samples, for the ordinal variables Mann-Whitney tests were used, and for the categorical ones, chi-square tests. Wilcoxon signed-rank tests were used to compare repeated ordinal measurements in the intervention group. Number of days and minutes spent reading Uncle Lightfoot, and number of minutes spent playing specific kind of games were summed up based on the Intervention Log for the whole intervention period, and used as continuous variables. Linear changes over time of continuous variables were analysed by mixed-design (split-plot) ANOVAs first, which were followed up by simple effect tests. Moderator and mediator variables regarding the intervention were first analysed by linear mixed effects models and then with Pearson’s correlations between the duration of CBT activities and change of certain variables over time.