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Exercise Interventions on Problematic Mobile Phone Use: a Multi-arm Randomized Controlled Trial

Effects of Aerobic Exercise or Tai Chi Chuan Interventions on Problematic Mobile Phone Use and the Potential Role of Intestinal Flora: a Multi-arm Randomized Controlled Trial

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05843591
Enrollment
90
Registered
2023-05-06
Start date
2022-02-04
Completion date
2022-06-10
Last updated
2023-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Exercise Intervention, Intestinal Flora, Randomized Clinical Trial, Tai Chi Chuan

Keywords

Problematic Mobile Phone Use, Exercise Intervention, Aerobic Exercise, Tai Chi Chuan, intestinal flora

Brief summary

Problematic mobile phone use (PMPU) has been described as a growing public health issue. This randomized controlled trial aimed to determine if aerobic exercise or Tai Chi Chuan as compared to the wait-list control group decreased PMPU-related symptoms; and to analyze the composition of the intestinal flora in the three study groups to explore the correlation between PMPU scores and flora species. A consecutive sample of 90 college students with PMPU was randomized to the aerobic exercise group (AE group, n = 30), the Tai Chi Chuan group (TCC group, n = 30), or the wait-list control group (WLC group, n = 30). The primary outcome was addiction symptoms, i.e., the PMPU score as assessed by the Smartphone Addiction Scale-Short Version (SAS-SV). Secondary outcomes were the emotion-related symptoms (depression, anxiety, self-esteem and self-efficacy), and physical-related symptoms (sleep quality, physical-fatigue and mental-fatigue). Intervention effects were analyzed via generalized estimated equation analysis (GEE).

Interventions

BEHAVIORALaerobic exercise or Tai Chi Chuan interventions

8-week aerobic exercise (AE group), 8-week Tai Chi Chuan training (TCC group)

Sponsors

Anhui Medical University
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to 22 Years
Healthy volunteers
No

Inclusion criteria

* (1) be 18 years or older; (2) college students; (3) fulfill the Smartphone Addiction Scale-Short Version (SAS-SV) criteria for PMPU; (4) have a low level of daily physical activity.

Exclusion criteria

* (1) regular practice of moderate and higher intensity exercise (Physical activity was measured using the Physical Activity Rating Scale-3 (PARS-3), which is a 3-item self-reported scale comprising intensity, duration and frequency \[14\]. Exercise was considered to be of more than moderate intensity when the PARS-3 scores was \>42); (2) any major disease (cardiovascular disease, respiratory illness, and musculoskeletal disorder) that can affect them to participate in exercise training; (3) any gastrointestinal diseases and other diseases affecting intestinal bacteria; and (4) any severe mental illness (e.g., depression, anxiety, bipolar disorder, obsessive-compulsive disorder, eating disorder, and post-traumatic stress disorder).

Design outcomes

Primary

MeasureTime frameDescription
Smartphone Addiction Scale-Short Version (SAS-SV)2 monthsProblematic mobile phone use levels

Secondary

MeasureTime frameDescription
Zung's Self Rating Depression Scale (SDS)2 monthsDepression levels
Zung's Self-Rating Anxiety Scale (SAS)2 monthsAnxiety levels
Rosenberg self-esteem scale (RSES)2 monthsSelf-esteem levels
General Self-Efficacy Scale (GSES)2 monthsSelf-Efficacy levels
Pittsburgh Sleep Quality Index (PSQI)2 monthsSleep Quality levels
Fatigue Scale-142 monthsphysical and mental fatigue levels
Intestinal flora2 monthsFecal microbial DNA was extracted using the QIAamp Fast DNA Stool Mini kit (Qiagen, Hilden, Germany) according to the manufacturer's instructions. All procedures of DNA extraction were performed in a class II biosafety cabinet. Universal primers (341F and 805R) linked with indices and sequencing adaptors were used to amplify the V3-V4 regions of the 16S rRNA gene. The amplification products were detected by agarose gel electrophoresis, and the amplification products were purified by nucleic acid purification beads to obtain the original library of the sample. The library quality was assessed on the Agilent Bioanalyzer 2100 system. The 16S rRNA gene amplification products sequencing was performed with the 2 × 250 bp paired-end method using the Illumina MiSeq Benchtop Sequencer \[48\] at the Genesky Biotechnologies Inc. (Shanghai, China).

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026