ChiCTR2500107921 版本V1.0 版本创建时间2025/08/21 08:53:50 中国临床试验注册中心

审核状态:

Project audit state:

通过审核

Successful

注册号:

Registration number:

ChiCTR2500107921 

最近更新日期:

Date of Last Refreshed on:

2025-08-21 08:53:42 

注册时间:

Date of Registration:

2025-08-21 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

BPL1乳清蛋白粉及功效成分对超重肥胖人群塑形和代谢指标的影响

Public title:

BPL1-Enriched Whey Protein Supplementation Modulates Body Composition and Metabolic Profiles in Overweight and Obese Adults

注册题目简写:

English Acronym:

研究课题的正式科学名称:

BPL1乳清蛋白粉及功效成分对超重肥胖人群塑形和代谢指标的影响

Scientific title:

BPL1-Enriched Whey Protein Supplementation Modulates Body Composition and Metabolic Profiles in Overweight and Obese Adults

研究课题代号(代码):

Study subject ID:

在二级注册机构或其它机构的注册号:

The registration number of the Partner Registry or other register:

申请注册联系人:

泮雯霏 

研究负责人:

张片红 

Applicant:

Wenfei Pan 

Study leader:

Pianhong Zhang 

申请注册联系人电话:

Applicant telephone:

+86 178 1687 8235

研究负责人电话:

Study leader's telephone:

+86 137 5711 9193

申请注册联系人传真 :

Applicant Fax:

研究负责人传真:

Study leader's fax:

申请注册联系人电子邮件:

Applicant E-mail:

3140102025@zju.edu.cn

研究负责人电子邮件:

Study leader's E-mail:

zph713@163.com

申请单位网址(自愿提供):

Applicant website(voluntary supply):

研究负责人网址(自愿提供):

Study leader's website(voluntary supply):

申请注册联系人通讯地址:

浙江省杭州市上城区解放路88号

研究负责人通讯地址:

浙江省杭州市上城区解放路88号

Applicant address:

No. 88, Jiefang Road, Shangcheng District, Hangzhou City, Zhejiang Province

Study leader's address:

No. 88, Jiefang Road, Shangcheng District, Hangzhou City, Zhejiang Province

申请注册联系人邮政编码:

Applicant postcode:

研究负责人邮政编码:

Study leader's postcode:

申请人所在单位:

浙江大学医学院附属第二医院营养科

Applicant's institution:

Department of Nutrition, Second Affiliated Hospital of Zhejiang University School of Medicine

研究负责人所在单位:

浙江大学医学院附属第二医院营养科

Affiliation of the Leader:

Department of Nutrition, Second Affiliated Hospital of Zhejiang University School of Medicine

是否获伦理委员会批准:

是/Yes

Approved by ethic committee:

Yes

伦理委员会批件文号:

Approved No. of ethic committee:

(2025)伦审研第(1185)号

伦理委员会批件附件:

Approved file of Ethical Committee:

查看附件View

批准本研究的伦理委员会名称:

浙江大学医学院附属第二医院人体研究伦理委员会

Name of the ethic committee:

Institutional Review Board (IRB), Second Affiliated Hospital, Zhejiang University School of Medicine

伦理委员会批准日期:

Date of approved by ethic committee:

2025-08-18 00:00:00

伦理委员会联系人:

吴志英

Contact Name of the ethic committee:

Zhiying Wu

伦理委员会联系地址:

浙江省杭州市上城区解放路88号

Contact Address of the ethic committee:

No. 88, Jiefang Road, Shangcheng District, Hangzhou City, Zhejiang Province

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 571 8778 3759

伦理委员会联系人邮箱:

Contact email of the ethic committee:

研究实施负责(组长)单位:

浙江大学医学院附属第二医院

Primary sponsor:

Second Affiliated Hospital, Zhejiang University School of Medicine

研究实施负责(组长)单位地址:

浙江省杭州市上城区解放路88号

Primary sponsor's address:

No. 88, Jiefang Road, Shangcheng District, Hangzhou City, Zhejiang Province

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

浙江

市(区县):

Country:

China

Province:

Zhejiang

City:

单位(医院):

浙江大学医学院附属第二医院

具体地址:

浙江省杭州市上城区解放路88号

Institution
hospital:

Second Affiliated Hospital, Zhejiang University School of Medicine

Address:

No. 88, Jiefang Road, Shangcheng District, Hangzhou City, Zhejiang Province

经费或物资来源:

健合(中国)有限公司

Source(s) of funding:

HEALTH AND HAPPINESS (H&H) CHINA LIMITED

Target disease:

Overweight and Obese

Target disease code:

研究类型:

干预性研究

Study type:

Interventional study

研究所处阶段:

其它 

Study phase:

N/A

研究设计:

随机平行对照 

Study design:

Parallel 

研究目的:

研究限能饮食下蛋白质及体重管理相关功效成分(BPL1+EGCG+余甘子)补充对超重肥胖人群进行抗阻运动后减重增肌的效果影响。  

Objectives of Study:

Effects of Protein and Weight-Management Functional Components (BPL1, EGCG, and Emblica officinalis) Supplementation under a Calorie-Restricted Diet on Weight Loss and Muscle Gain in Overweight and Obese Individuals Following Resistance Training.

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

1.年龄25~45周岁,性别不限; 2.Body Mass Index (BMI):24-29.9kg/m^2; 3.积极参与休闲活动但至少1年未参加结构化重量训练; 4.日常蛋白质摄入量低于~1.6g/kg; 5.自愿同意并签署知情同意书。

Inclusion criteria

1. Adults aged 25–45 years, male or female; 2. Body Mass Index (BMI) between 24.0 and 29.9 kg/m^2; 3. Engaged in leisure-time physical activity but not in structured resistance training for at least 12 months; 4. Habitual protein intake < ~1.6 g/kg body weight per day; 5. Willing and able to provide written informed consent.

排除标准:

1.吸烟、饮酒、熬夜等不良嗜好; 2.过去一年内服用任何类固醇补充剂、以及其他有助于蛋白质合成的补充剂成分(如HMB、肌酸、BCAA等); 3.任何不受控制的代谢紊乱或心血管疾病,包括心脏病、高血压病史、糖尿病、甲状腺疾病、性腺功能低下; 4.肝肾、肌肉骨骼、自身免疫或神经系统、精神疾病; 5.患有影响食物消化吸收的疾病(如慢性腹泻、便秘、严重消化道炎症、活动性消化道溃疡、胃肠道切除术后等); 6.对产品成分过敏或有先天性代谢障碍; 7.妊娠或哺乳期,或有严重痛经、经期严重不规律; 8.研究者认为其它不适于参与本研究的情况(如患有未列入排除标准的严重疾病)。

Exclusion criteria:

1. Current smoking, excessive alcohol use, or other unhealthy lifestyle habits (e.g., chronic sleep deprivation); 2. Use of anabolic steroids or protein-synthesis–enhancing supplements (e.g., HMB, creatine, BCAAs) within the past year; 3. Uncontrolled metabolic or cardiovascular disorders, including heart disease, hypertension, diabetes, thyroid dysfunction, or hypogonadism; 4. Clinically significant hepatic, renal, musculoskeletal, autoimmune, neurological, or psychiatric disorders; 5. Gastrointestinal diseases impairing nutrient digestion or absorption (e.g., chronic diarrhea, severe inflammation, active peptic ulcer, or history of major GI surgery); 6. Known allergy to study product ingredients or congenital metabolic disorders; 7. Pregnancy, lactation, or significant gynecological issues (e.g., severe dysmenorrhea, marked menstrual irregularity); 8. Any other condition considered by the investigators to render the participant unsuitable for the study.

研究实施时间:

Study execute time:

From 2025-08-31 00:00:00 To 2027-03-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2025-08-31 00:00:00 To 2026-08-31 00:00:00  

干预措施:

Interventions:

组别:

安慰剂组

样本量:

35

Group:

Placebo group

Sample size:

干预措施:

全程限能饮食结合抗阻运动,每周4天,共12周,在运动前30分钟内饮用1条安慰剂。

干预措施代码:

Intervention:

Participants will follow a calorie-restricted diet and perform resistance training four days per week, while consuming one sachet of placebo within 30 minutes prior to exercise, for a total intervention period of 12 weeks.

Intervention code:

组别:

蛋白质补充剂组

样本量:

35

Group:

Protein supplement group

Sample size:

干预措施:

全程限能饮食结合抗阻运动,每周4天,共12周,在运动前30分钟内饮用1条蛋白质补充剂。

干预措施代码:

Intervention:

Participants will follow a calorie-restricted diet and perform resistance training four days per week, while consuming one sachet of protein supplements within 30 minutes prior to exercise, for a total intervention period of 12 weeks.

Intervention code:

组别:

功效成分补充剂组

样本量:

35

Group:

Functional ingredient supplement group

Sample size:

干预措施:

全程限能饮食结合抗阻运动,每周4天,共12周,在运动前30分钟内饮用1条功效成分补充剂

干预措施代码:

Intervention:

Participants will follow a calorie-restricted diet and perform resistance training four days per week, while consuming one sachet of active supplements within 30 minutes prior to exercise, for a total intervention period of 1

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

浙江 

市(区县):

 

Country:

China 

Province:

Zhejiang 

City:

 

单位(医院):

浙江大学医学院附属第二医院 

单位级别:

三甲 

Institution
hospital:

Second Affiliated Hospital, Zhejiang University School of Medicine

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

空腹血糖

指标类型:

主要指标

Outcome:

Fasting blood glucose

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

糖化血红蛋白

指标类型:

主要指标

Outcome:

Glycated hemoglobin

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

糖化白蛋白

指标类型:

主要指标

Outcome:

Glycated albumin

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

空腹胰岛素

指标类型:

主要指标

Outcome:

Fasting insulin

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

胰高血糖素样肽-1

指标类型:

主要指标

Outcome:

Glucagon-like peptide-1

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

甘油三酯

指标类型:

主要指标

Outcome:

Triglycerides

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

总胆固醇

指标类型:

主要指标

Outcome:

Total cholesterol

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

体重

指标类型:

主要指标

Outcome:

Body weight

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

体脂率

指标类型:

主要指标

Outcome:

Body fat percentage

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

瘦体重

指标类型:

主要指标

Outcome:

Lean body mass

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

采集人体标本:

Collecting sample(s)
from participants:

标本中文名:

血液

组织:

Sample Name:

blood

Tissue:

人体标本去向

使用后销毁  

说明

Fate of sample:

Destruction after use  

Note:

标本中文名:

粪便

组织:

Sample Name:

feces

Tissue:

人体标本去向

使用后销毁  

说明

Fate of sample:

Destruction after use  

Note:

征募研究对象情况:

Recruiting status:

尚未开始

Not yet recruiting

年龄范围:

Participant age:

最小 Min age years
最大 Max age years

性别:

男女均可

Gender:

Both

随机方法(请说明由何人用什么方法产生随机序列):

随机序列由R语言创建

Randomization Procedure (please state who generates the random number sequence and by what method):

The randomization sequence will be generated in R

是否公开试验完成后的统计结果:

Calculated Results after the Study Completed public access:

公开/Public

盲法:

对研究者和受试者设盲

Blinding:

Blinding of the investigator and subject

试验完成后的统计结果(上传文件):

Calculated Results after
the Study Completed(upload file):

是否共享原始数据:

IPD sharing

No

共享原始数据的方式(说明:请填入公开原始数据日期和方式,如采用网络平台,需填该网络平台名称和网址):

The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url):

None

数据采集和管理(说明:数据采集和管理由两部分组成,一为病例记录表(Case Record Form, CRF),二为电子采集和管理系统(Electronic Data Capture, EDC),如ResMan即为一种基于互联网的EDC:

病例记录表和电子采集和管理系统

Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture:

Case Record Form, CRF/Electronic Data Capture, EDC

数据与安全监察委员会:

Data and Safety Monitoring Committee:

暂未确定/Not yet

注册人:

Name of Registration:

 2025-08-21 08:53:42