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Mental Health Survey and Creatine Supplementation Program for Adolescent Athletes at the Shanghai Sports School

Mental Health Survey and Creatine Supplementation Program for Adolescent Athletes at the Shanghai Sports School

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600116330
Enrollment
Unknown
Registered
2026-01-08
Start date
2025-11-01
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Anxiety

Interventions

Placebo control group:Normal diet and routine training plus 150 mL of water per day
Intervention group (creatine supplementation):Normal diet and routine training plus 3 g of creatine dissolved in 150 mL of water per day

Sponsors

Huashan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
11 Years to 18 Years

Inclusion criteria

Inclusion criteria: 1. Inclusion Criteria for Participants in the Current Status Survey(Participants meeting all of the following criteria were included): (1)Adolescent athletes currently enrolled at the Shanghai Sports School, with no restrictions on gender, grade level, or sport, aged 11–18 years; (2)Participants who provided written informed consent. 2. Inclusion Criteria for Participants in the Randomized Controlled Trial: (1)Adolescent athletes currently enrolled at the Shanghai Sports School, with no restrictions on sex, grade level, or sport, aged 11–18 years; (2)A score of 45 or higher on the Self-Rating Anxiety Scale (SAS); (3)At least one year of regular sports training experience, with a training frequency of at least 3–4 sessions per week; (4)No history of cardiovascular disease, diabetes, hepatic or renal insufficiency, or other health conditions that may affect exercise performance; (5)No history of sports-related injuries, particularly injuries involving body regions relevant to the sport participated in, such as the shoulder, knee, or spine; (6)No use of creatine or other performance-enhancing supplements within three months prior to the start of the trial; (7)Relatively stable and regular dietary habits, with no engagement in extreme weight-loss diets or very high-protein diets; (8)Provision of written informed consent.

Exclusion criteria

Exclusion criteria: 1. Exclusion Criteria for Participants in the Current Status Survey(Participants meeting any of the following criteria were excluded): (1)Failure to provide written informed consent; (2)Unwillingness or inability to continue participation in the survey, or withdrawal of informed consent; (3)Discovery after enrollment that the participant did not meet the inclusion criteria or met any exclusion criteria; (4)Determination by the investigators that continued participation would be detrimental to the participant; (5)Termination of the survey by the investigators. 2. Exclusion Criteria for Participants in the Randomized Controlled Trial: (1)Presence of any known chronic diseases, such as diabetes mellitus, cardiovascular disease, or chronic kidney disease, that may affect athletic performance or metabolism; (2)A history of severe sports-related injuries, such as fractures or surgical history involving the knee, shoulder, or spine; (3)Use of creatine or other performance-enhancing supplements within three months prior to the start of the trial; (4)Engagement in strict dieting or adherence to a very low-calorie diet; (5)Adherence to extreme vegetarian diets or other special dietary patterns; (6)Recent participation in extreme training programs or major changes in training regimen; (7)Presence of cognitive impairment or psychiatric disorders that may limit the participant’s ability to understand the study requirements or comply with study procedures; (8)Failure to provide written informed consent; (9)Unwillingness or inability to continue participation in the trial, or withdrawal of informed consent; (10)Discovery after enrollment that the participant did not meet the inclusion criteria or met any exclusion criteria; (11)Determination by the investigators that continued participation would be detrimental to the participant; (12)Termination of the study by the investigators.

Design outcomes

Primary

MeasureTime frame
Anxiety rating scale (Self-Rating Anxiety Scale, SAS);

Secondary

MeasureTime frame
Anxiety rating scale(Screen for Child Anxiety Related Emotional Disorders, SCARED);Anxiety rating scale(State–Trait Anxiety Inventory, STAI);Sleep quality scale(Pittsburgh Sleep Quality Index, PSQI);Handgrip strength (kg);Body weight (kg);Skeletal muscle mass (kg);Fat mass (kg);Waist-to-hip ratio;Erythrocyte creatine (µmol/g Hb);

Countries

China

Contacts

Public ContactShao Chunhai

Huashan Hospital, Fudan University

2257139538@qq.com+86 137 9540 4367

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026