Study design and participants
This study used a parallel-grouped randomised control trial (RCT) design where the control group received a placebo intervention. Documenting this study was conducted following CONSORT guidelines. The target population was preclinical medical and dental students at Umm Al-Qura University (UQU), Makkah, Saudi Arabia in the 2012–2013 academic year. The students’ age range was 20–22 years. The preclinical medical and dental students study a traditional curriculum (lecture-based) with compulsory course unit structure, and they are assessed by essays, multiple-choice and objective structured clinical examination. The medical/dental programme is composed of one orientation year, two preclinical years (2nd–3rd) and three clinical years (4th–6th), followed by an internship year. Each academic year is composed of two terms with a summer vacation. Eligibility criteria were (a) being a medical or dental student; (b) being a second- or third-year student; and (c) studying at UQU. Exclusion criteria included students who (a) attended the interventional programme during the course of their academic study, (b) under psychological treatments or drugs regimen or (c) did not sign the study consent form.
A sample size of 130 (65 at each group) participants was needed to detect a difference between the two groups. A study power of 90 %, type I error of 5 %, minimal clinical difference of 4 points in any of the psychological health means, and an average standard deviation of 7, derived from a recent well-designed coaching RCT which used the Depression Anxiety Stress Scale (DASS-21) [20], were used in the sample size calculation. The resulting number (130) for the two groups was multiplied by 1.5 for the design effect (multiple follow-up), yielding a desired sample size of 196 in both groups. This number was again multiplied by 1.5 for the estimated non-response rate (50 %) and multiplied by 1.25 for estimated drop-out during the follow-up (20 %), with the result that 366 students needed to be approached.
Setting
The study was advertised via large roll-up posters, and students were recruited in the first term via invitation envelopes which contained coloured flyers about the programmes, a study information sheet and the consent form. After receiving participants’ signed consent, participants were randomly allocated into the intervention group (IG) and control group (CG) by the principal investigator. Randomisation was achieved using a computer-generated random number list. The intervention was conducted during the first week of the second term. Students knew their assigned group one week before both programmes were conducted. However, the students and research assistants who managed the study protocol and data collection were blinded to the participants’ group allocation. Thus, the study was partially blinded. Students were assessed three times in the second term, as follows: Week 1 (T1), immediately before the programme was conducted; Week 2 (T2), a week after the programme; and Week 6 (T3), five weeks after the programme concluded. The questionnaires were disseminated and collected between students’ lecture breaks.
Intervention
Students in the IG attended a self-development coaching programme titled “How to Be an Ultra Super Student” (HBUSS), while the control group received a normal lecture-type programme titled “Learning and Success in Health Faculties” (LSHF). Each programme was delivered as a live course in a large lecture theatre during students’ free time in Week 1 of the second term; participants in both groups were supplied with the appropriate programme booklet and audio CD. Due to cultural and religious considerations in Saudi Arabia, male and female seats were separated by a barrier along the theatre, but facing the coach, on the intervention days.
The HBUSS is a self-development coaching programme, which has been developed and run by the lead author, who is a self-development coach and trainer, since 2008 [19]. The contents were derived from the coach’s personal experiences with coaching and from reading and practicing self-development over a number of years. The programme aimed mainly to improve students’ academic performance and psychological health. It did not use psychological therapeutic approaches, but rather focussed on a series of skills and conceptual ideas about studying and coping with challenges during the academic journey.
On the other hand, the LSHF programme was developed by the first author for the purpose of this study only. It provided information about learning in health faculties and the factors leading to success according to a scientific literature review. It also briefly touched on the scientific research area. The information in the LSHF programme was taken from academic articles or books; however, it did not have a practical aim to improve students’ performance or psychology. Both programs were presented by the first author. The programmes’ modules, CD contents, approach and duration are detailed in Table 1.
Table 1 Comparison between the intervention and control programmes While the presenter was careful to follow the intervention and active control group manuals, no independent assessment of treatment fidelity was performed. In addition, while the participants’ attendance was tracked, there was no assessment of completion of quizzes or assignments associated with the workshop material in order to assess the participants’ understanding of the material. This was not done as it is not a common practice for self-development coaching programs, in contrast to other formal training courses, and so would have altered the participants’ experience of a typical self-development coaching program.
Assessment
Hard copies of the self-report questionnaire were used. Three aspects were assessed, as follows: (a) psychological health at T1, T2 and T3; (b) participants’ levels of belief in the effectiveness of the programme, considered both logically and emotionally at T1 and T2; and (c) students’ academic performance before and after the intervention.
Psychological health was measured using the DASS-21 [21, 22], General Self-Efficacy scale (GSE) [23], and Satisfaction With Life Scale (SWLS) [24]. The DASS-21 measured negative aspects of students’ psychological health, while GSE and the SWLS measured positive aspects of students’ psychological health. The DASS-21 is composed of 21 questions to assess depression, anxiety and stress subclasses, which are measured by the sum of the 7 corresponding questions. Each question can be answered from 0 “Did not apply to me at all” to 3 “Applied to me very much, or most of the time”. A high DASS-21 subclass score indicates unfavourable status. DASS-21 has excellent psychometric properties, with a Cronbach’s alpha of 0.82 to 0.90 for each subscale [25]. GSE is composed of 10 questions to measure self-efficacy, and each question can be answered from 1 “Not at all true” to 4 “Exactly true”. GSE has a Cronbach’s alpha of .86 among 25 nations [26]. Finally, the SWLS is composed of five questions to measure life satisfaction, and each question can be answered from 7 “Strongly agree” to 1 “strongly disagree”. SWLS has a Cronbach’s alpha of .87 [27, 28]. High SWLS or GSE sum-scores indicate high satisfaction or self-efficacy.
In addition, the Credibility and Expectancy Questionnaire (CEQ) [29] was used to investigate participants’ perception levels of the programme’s success, both logically (credibility) and emotionally (expectancy). This is a 6-item scale, with some answers ranging from 1 “Not at all confident” to 9 “Very confident”, and others ranging from 0–100 %. The Cronbach’s alpha of the CEQ is .85 [29]. The validated Arabic versions of the DASS-21 and GSE were used [26, 30], while the SWLS and CEQ were face and content validated and translated into Arabic in the pilot study [19] using World Health Organization (WHO) translation guidelines [31].
Academic performance was measured by students’ weighted grades (WG), in the first term before the intervention and at the end of the second term, four months after the intervention. WG were measured according to the following equation:
$$ \mathrm{Weighted}\ \mathrm{grade}\ \mathrm{percentage}\ \left(\mathrm{W}\mathrm{G}\right)={\displaystyle \sum }\ \frac{\left(\mathrm{each}\ {\mathrm{unit}}^{\hbox{'}}\mathrm{s}\ \mathrm{grade}\mathrm{s}\ *\ {\mathrm{unit}}^{\hbox{'}}\mathrm{s}\ \mathrm{credit}\ \mathrm{hours}\right)}{\left(\ \mathrm{total}\ \mathrm{units}\ \mathrm{credit}\ \mathrm{hours}\right)}*10 $$
Student’s grades were obtained from faculties’ administrative offices after receiving the students’ approval. Demographic data included faculty, academic year, gender, family income, marital status and nationality. All identifying information was destroyed after data completion and the data were treated anonymously.
Incentives and ethical considerations
Participation in the study was voluntary. All participants received the interventional or placebo programmes without charge. Students received two certificates of appreciation, one upon attending the designated programme, and one after completing all the follow-ups. All attending students were entered in three random prize draws for 50 Saudi Riyal (13.33 U.S dollar) vouchers in each programme.
The study was approved by the Queensland University of Technology ethical committee. As an institutional ethics board had not been formally established at UQU, formal approvals were obtained from the medical and dental faculties at UQU, in addition to the students’ signed consent.
Randomisation
Participants were stratified by faculty, gender, and academic year, and then randomised into the IG and CG using computer-generated random number lists by the principal investigator. Stratified randomisation was conducted mainly to overcome the unbalanced medical/dental student ratio. Neither students nor research assistants were aware of which students were allocated to the IG and CG until the first day of the second term.
Data analysis
SPSS software package version 21 was used to assist in data analysis. Chi-square and Fisher’s exact tests were employed to test the demographic variable differences between the groups. A t-test was used to compare the baselines of the DASS-21 subgroups, GSE, SWLS and CEQ. After splitting data by group, repeated measures analysis of variance (rANOVA) was used to test the difference between T1 to T2, T2 toT3 and T2 to T3 for the IG and CG. Factorial rANOVA was used to analyse the differences in all the outcome variables between IG and CG. Bonferroni correction was used for the rANOVA post hoc test.