Centre For Clinical Research And Biostatistics (CCRB)

Back History

1 Unique Trial Number (assigned by CCRB)

CUHK_CCRB00539

2 Trial Registration Date

2016-12-20

iRegistration Status

Prospective

3 Secondary IDs

2016.558

4 Source(s) of Funding

NA

5 Primary Sponsor

NA

6 Secondary Sponsor

NA

Function

Not Applicable

Please specify

7Responsible Contact Person (public contact person for patients interested in participating)

i Name

Yiu Yun Sang

ii Address

office 4, 1F, Block F,
Department of OG,
Prince of Wales Hospital,
30-32 Ngan Shing Street,
Shatin, N.T.
Hong Kong

iii Phone

3505 1764

iv Email

sandyyiu@cuhk.edu.hk

v Affiliation

Obstetric and gynaecology, CUHK

vi Country

Hong Kong

8Research Contact Person (person to contact for scientific inquiries)

i Name

YIU LEUNG CHAN

ii Address

office 4, 1F, Block F,
Department of OG,
Prince of Wales Hospital,
30-32 Ngan Shing Street,
Shatin, N.T.
Hong Kong

iii Phone

26323199

iv Email

cylcps@yahoo.com.hk

v Affiliation

Obstetric and gynaecology, CUHK

vi Country

Hong Kong

9 Official Scientific Title of the Study

The effect of physical activity on sperm quality

10 Public Title

The effect of physical activity on sperm quality

i Public Title in Chinese 研究名稱

身體活動對精子質素的影響

11 Short Title (Optional)

The effect of physical activity on sperm quality

12 Countries of Recruitment

Hong Kong

13Research Ethic Review

i Has the study received appropriate ethics approval?

Yes

ii When is the approval date?

2016-11-29

iii Full Name of IRB/IEC

Joint CUHK-NTEC Clinical Research Ethics Committee

Please specify

iv IRB/IEC approval reference number

2016.558

14 Medical Condition Being Studied

Sperm quality

physical activity

15Intervention

i Types of intervention

Other

Please specify

no intervention will be provided.

ii Description/ name of Intervention/article

all the participant will be provided a portable accelerometer for 7 days to measure their activity activity

iii Dosage form of the intervention

This is not a drug trial

iv Dosage of the intervention

This is not a drug trial

v Duration of the intervention

This is not a drug trial

vi Frequency of the intervention

This is not a drug trial

16Comparative Treatments

i Description/ name of comparative treatments

There is no comparative treatments. All the participant will be provided a portable accelerometer for 7 days to measure their activity activity

ii Dosage form of the comparative treatments

This is not a drug trial

iii Dosage of the comparative treatments

This is not a drug trial

iv Duration of the comparative treatments

This is not a drug trial

v Frequency of the comparative treatments

This is not a drug trial

17Key Inclusion and Exclusion Criteria

i Inclusion Criteria

Non azoospermic

No known genetic defects

ii Exclusion Criteria

azoospermic

Phenotypically abnormal

iii Age Minimum

18

iv Age Maximum

75

v Gender

Male

18 Study Type

Observational

19Study Design

i Randomization

Non-randomized

Please specify

ii Nature of control

Not Applicable

iii Degree of masking

Not Applicable

If Single-blind, who will be masked?

iv Group Assignment

Not Applicable

v Study Phase

Other

Please specify

This is not a drug trial

vi Study Objectives (Optional)

The aim of this study is to investigate the relations between PA and semen quality in a given period in order to understand underlying mechanism on fluctuation in different semen parameters.

20 Anticipated trial start date

2016-12-26

21 Target Sample Size

200

22 Recruitment Status

Recruiting

23Primary Outcome

iThe Name of the outcome

measure intensity of physical activity (PA)

iiThe metric or method of measurement used

a portable accelerometer will be provided for 7 days to measure PA

iiiThe timepoint(s) of primary interest

7 days

24Secondary Outcome

iThe Name of the outcome

semen quality

iiThe metric or method of measurement used

semen analysis

iiiThe timepoint(s) of primary interest

day of recruitment and after 7 days of recruitment

Secondary Outcome

iThe Name of the outcome

measure hormonal testing and other biochemical molecules such as enzyme or amino acid

iiThe metric or method of measurement used

blood sampling ( 5 - 10 ml blood)

iiiThe timepoint(s) of primary interest

day of recruitment and after 7 days of recruitment

25Study Information/Publication

i Study Information/Publication Available?

No

ii Link to Study Information/Publication

26Last Update Date

2020-10-30

27 Primary Registry and Trial Identifying Number

ChiCTR-ROC-16010246

28 Date of Registration in Primary Registry

2016-12-20

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Trial Detail