Study Smart! Effectiveness of a Smartphone Use Intervention on Students' Performance and Well-being
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| ClinicalTrials.gov Identifier: NCT04550286 |
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Recruitment Status :
Recruiting
First Posted : September 16, 2020
Last Update Posted : June 8, 2021
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Smartphone use in academic contexts (e.g., in lectures or while studying for an exam) appears to go along with negative effects on students' academic performance (i.e., concentration, perceived learning achievement, and grades) and well-being (e.g., anxiety, positive and negative affect). Despite these alarming effects, intervention studies aiming at reducing smartphone interference are generally scarce and evidential inconsistent. For instance, existing studies suggest that short separation phases from smartphones accelerate anxiety and lead to cravings and smartphone overuse after the separation period. Other studies, however, conclude that separation phases enhance individual well-being and academic performance.
RESEARCH QUESTIONS. The present study aims at rigorously studying the effects of smartphone separation during exam phases on university students' performance and well-being. To do so, smartphone use reduction is incorporated into students' everyday life and encouraged through a planning intervention. The main research questions concern whether the intervention can reduce smartphone use in students, whether planning is effective in this regard, whether the intervention positively affects students' academic performance (e.g., concentration, perceived performance, grades), and whether the intervention enhances students' well-being (e.g., increased positive and decreased negative affect, lower anxiety). Furthermore, possible moderating (e.g., smartphone dependence, FoMO) and mediating variables (e.g., exam preparation-related flow, smartphone usage time, used mobile applications) are examined.
METHOD. Students are to develop action plans (BCT 1.4; plans on how to reduce smartphone use during exam phases) and coping plans (BCT 1.2; plans on how to uphold reduced smartphone use during exam phases despite potential stressors or urges). The relevant variables are assessed over the course of 5 measurement points (t1-t3 take place on a weekly basis, t4 takes place after the last exam, t5 takes place 2 months after t4). Furthermore, smartphone use (smartphone use time, used mobile applications) is objectively measured via a mobile application.
| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Experimental Group: Smartphone Use Reduction Control Group | Behavioral: Smartphone Use Reduction in Academic Context Behavioral: Control | Not Applicable |
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| Study Type : | Interventional (Clinical Trial) |
| Estimated Enrollment : | 140 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | Single (Participant) |
| Primary Purpose: | Prevention |
| Official Title: | Study Smart! A Randomized Control Trial Examining the Effectiveness of an Individual Planning Intervention to Reduce Smartphone Interferences on Students' Academic Performance and Well-being |
| Actual Study Start Date : | January 13, 2020 |
| Estimated Primary Completion Date : | October 31, 2021 |
| Estimated Study Completion Date : | October 31, 2021 |
| Arm | Intervention/treatment |
|---|---|
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Experimental: Intervention Group
Intervention points in time include:
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Behavioral: Smartphone Use Reduction in Academic Context
Students will be given general advice on how to organize their exam preparation environment and behavior to improve their overall learning performance (e.g., organization of materials for exam preparation, pauses during exam preparation). This refers to the behavior change techniques (BCT 4.1, instructions on how to perform the behavior; Michie et al.; 2013). In the next step, participants in the intervention group complete planning sheets. Each student has to develop up to three action plans (BCT 1.4) including when, where, and for how long the smartphone will be put away during the daily exam preparation period (cf. Radtke et al., 2018). In addition, each participant should try to anticipate possible barriers to engaging in the planned behavior and plan what he or she could do to overcome these possible barriers (i.e., coping planning; BCT 1.2; Michie et al., 2013). |
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Active Comparator: Control Group
Control points in time include all parts except for number 4. Here students in the control group will receive questionnaires on general health behavior in order to achieve an equal questionnaire completion time compared to the intervention group.
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Behavioral: Control
Students will be given general advice on how to organize their exam preparation environment and behavior to improve their overall learning performance (e.g., organization of materials for exam preparation, pauses during exam preparation). |
- Objective measure of smartphone use [ Time Frame: Continuously from time point 1 (baseline) through time point 2 (1 weeks after baseline), time point 3 (2 weeks after baseline) to time point 4 (after final exam in the current semester, approx. 4 - 6 weeks after baseline) ]The daily smartphone use will be assessed via the mobile application Murmuras measuring daily smartphone use in minutes and specific application use concerning the 10 most used applications.
- Subjective measure of academic performance: Ability to concentrate [ Time Frame: Time point 1 (baseline), time point 2 (1 week after baseline), time point 3 (2 weeks after baseline), time point 4 (after final exam in the current semester, approx. 4 - 6 weeks after baseline) ]
Changes in students' ability to concentrate will be assessed through subjective self-report measures.
Measure: LIST; Inventory for assessing learning strategies in students; score: 1 [not at all agreed] to 5 [completely agreed]).
- Subjective measure of academic performance: Experienced study-related stress [ Time Frame: Time point 1 (baseline), time point 2 (1 week after baseline), time point 3 (2 weeks after baseline) ]
Changes in students' experienced study-related stress will be assessed through subjective self-report measures.
Measure: Self-developed based on STQL-S; Stress coping and quality of life in students; score: 1 [not at all] to 5 [extremely]).
- Subjective measure of academic performance: Perceived learning achievement [ Time Frame: Time point 4 (after final exam in the current semester, approx. 4 - 6 weeks after baseline) ]
Students' perceived learning achievement will be assessed through subjective self-report measures.
Measure: Self-developed. Measure: Self-developed; score: 1 [not at all agreed] to 6 [completely agreed]).
- Subjective measure of academic performance: Exam grades [ Time Frame: Time point 5 (2 months after final exam in the current semester) ]Students' exam grades will be assessed through subjective self-report measures. Measure: Self-developed.
- Subjective measure of well-being: Positive and negative affect [ Time Frame: Time point 1 (baseline), time point 2 (1 week after baseline), time point 3 (2 weeks after baseline), time point 4 (after final exam in the current semester, approx. 4 - 6 weeks after baseline) ]
Changes in students' positive and negative affect will be assessed through subjective self-report measures.
Measure: PANAS; Positive and negative affect schedule; score: 1 [not at all] to 5 [extremely]).
- Subjective measure of well-being: Anxiety [ Time Frame: Time point 1 (baseline), time point 2 (1 week after baseline), time point 3 (2 weeks after baseline), time point 4 (after final exam in the current semester, approx. 4 - 6 weeks after baseline) ]
Changes in students' anxiety will be assessed through subjective self-report measures.
Measure: PSS; Perceived stress scale - German version; score: 1 [never] to 5 [very often]).
- Subjective measure of well-being: Subjective well-being [ Time Frame: Time point 1 (baseline), time point 2 (1 week after baseline), time point 3 (2 weeks after baseline), time point 4 (after final exam in the current semester, approx. 4 - 6 weeks after baseline) ]
Changes in students' subjective well-being will be assessed through subjective self-report measures.
Measure: WHO-5 Well-being-Index; score: 1 [never] to 6 [all the time]).
- Subjective measure of moderating variables: Smartphone dependence [ Time Frame: Time point 1 (baseline) ]
The possible moderator smartphone dependence will be assessed through subjective self-report measures.
Measure: Quick test for smartphone addiction; score: 1 [not at all agreed] to 6 [completely agreed]).
- Subjective measure of moderating variables: Fear of missing out [ Time Frame: Time point 1 (baseline) ]
The possible moderator fear of missing out (FoMO) will be assessed through subjective self-report measures.
Measure: FoMOs; Fear of missing out scale; score: 1 [not at all agreed] to 5 [completely agreed]).
- Subjective measure of mediating variables: Individual action planning [ Time Frame: Time point 1 (baseline), time point 2 (1 week after baseline), time point 3 (2 weeks after baseline), time point 4 (after final exam in the current semester, approx. 4 - 6 weeks after baseline) ]
Changes in the possible mediator individual action planning will be assessed through subjective self-report measures.
Measure: According to the Health Action Process Approach [HAPA]; score: 1 [not at all agreed] to 6 [completely agreed])
- Subjective measure of mediating variables: Individual coping planning [ Time Frame: Time point 1 (baseline), time point 2 (1 week after baseline), time point 3 (2 weeks after baseline), time point 4 (after final exam in the current semester, approx. 4 - 6 weeks after baseline) ]
Changes in the possible mediator individual coping planning will be assessed through subjective self-report measures.
Measure: According to the Health Action Process Approach [HAPA]; score: 1 [not at all agreed] to 6 [completely agreed]).
- Subjective measure of mediating variables: Exam preparation-related flow [ Time Frame: Time point 1 (baseline), time point 2 (1 week after baseline), time point 3 (2 weeks after baseline), time point 4 (after final exam in the current semester, approx. 4 - 6 weeks after baseline) ]
Changes in the possible mediator exam preparation-related flow will be assessed through subjective self-report measures.
Measure: FKS; Flow-short scale; score: 1 [not at all agreed] to 5 [completely agreed]).
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| Ages Eligible for Study: | 16 Years and older (Child, Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- Students from universities and universities of applied science
- At least one written or oral exam during the data collection period
- Ownership of an Android smartphone
- Daily usage of the smartphone
- Experience of distractions due to the smartphone during exam phases
- At least 16 years of age
- At least good German language skills
Exclusion Criteria:
- Withholding consent to the data security regulations
- Withholding consent to the installation of the study application
- Students who are currently being treated for exam anxiety
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04550286
| Contact: Tania R. Nunez, M.A. | +49 (0)2302/926-884 | tania.nunez@uni-wh.de | |
| Contact: Theda Radtke, PhD | theda.radtke@uni-wh.de |
| Germany | |
| Witten/Herdecke University | Recruiting |
| Witten, NRW, Germany, 58454 | |
| Contact: Theda Radtke, Prof. Dr. Theda.Radtke@uni-wh.de | |
| Contact: Tania Nuñez, Msc Tania.Nunez@uni-wh.de | |
| Principal Investigator: | Theda Radtke | Witten/Herdecke University |
| Responsible Party: | Theda Radtke, Prof. Dr., University of Witten/Herdecke |
| ClinicalTrials.gov Identifier: | NCT04550286 |
| Other Study ID Numbers: |
215/2019 |
| First Posted: | September 16, 2020 Key Record Dates |
| Last Update Posted: | June 8, 2021 |
| Last Verified: | June 2021 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | Yes |
| Plan Description: | The data underlying publications will be shared to make the published results reproducible. |
| Time Frame: | The data underlying publications will be shared to make the published results reproducible after submission of the papers. |
| Access Criteria: | Upon request |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |

