Centre For Clinical Research And Biostatistics (CCRB)

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1 Unique Trial Number (assigned by CCRB)

CUHK_CCRB00543

2 Trial Registration Date

2016-12-28

i Registration Status

Prospective

3 Secondary IDs

2016.A5.023.16C

4 Source(s) of Funding

Public Policy Research (PPR) Funding Scheme, Central Policy Unit of the Hong Kong Special Administrative Region Government

5 Primary Sponsor

The Education University of Hong Kong

6 Secondary Sponsor

City University of Hong Kong

Function

Form a group with the primary sponsor in which the responsibilities of sponsorship are allocated among the members of the group

Please specify

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

i Name

Kee Lee Chou

ii Address

Department of Asian and Policy Studies
The Education University of Hong Kong
Tai Po, N.T.
Hong Kong

iii Phone

2948 7473

iv Email

klchou@eduhk.hk

v Affiliation

The Education University of Hong Kong

vi Country

China

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

i Name

Kee Lee Chou

ii Address

Chair Professor of Social Policy
Department of Asian and Policy Studies
The Education University of Hong Kong
Tai Po Campus
10 Lo Ping Road,
Tai Po, New Territories, Hong Kong

iii Phone

2948 7474

iv Email

klchou@eduhk.hk

v Affiliation

Department of Asian and Policy Studies, The Education University of Hong Kong

vi Country

China

9 Official Scientific Title of the Study

Promotion of Volunteerism among Hong Kong Retirees: An Intervention Study

10 Public Title

Promotion of Volunteerism among Hong Kong Retirees: An Intervention Study

i Public Title in Chinese 研究名稱

提升香港退休人仕參與自願服務的程度：介入研究

11 Short Title (Optional)

12 Countries of Recruitment

China

13 Research Ethic Review

i Has the study received appropriate ethics approval?

Yes

ii When is the approval date?

2016-05-13

iii Full Name of IRB/IEC

Other

Please specify

Human Research Ethics Committee (HREC) at The Hong Kong Institute of Education

iv IRB/IEC approval reference number

2015-2016-0324

14 Medical Condition Being Studied

none

15 Intervention

i Types of intervention

Behavior

Please specify

ii Description/ name of Intervention/article

Theory-based face-to-face social-cognitive group intervention to promote volunteering

iii Dosage form of the intervention

face-to-face group intervention

iv Dosage of the intervention

1 hour per session

v Duration of the intervention

4 weeks

vi Frequency of the intervention

once per week

16 Comparative Treatments

i Description/ name of comparative treatments

Theory-based face-to-face social-cognitive group intervention to promote physical activity

ii Dosage form of the comparative treatments

face-to-face group intervention

iii Dosage of the comparative treatments

1 hour per session

iv Duration of the comparative treatments

4 weeks

v Frequency of the comparative treatments

once per week

17 Key Inclusion and Exclusion Criteria

i Inclusion Criteria

65 years old and older

ii Exclusion Criteria

acutely physically impaired or disabled

seriously cognitive impaired or severely depressed

engaged in any formal volunteering work in the past year

working on full- or part-time basis

iii Age Minimum

65

iv Age Maximum

999

v Gender

Both Male and Female

18 Study Type

Interventional

19 Study Design

i Randomization

Randomized

Please specify

group nature of the intervention therefore a stratified randomization of local community centres

ii Nature of control

Active

iii Degree of masking

Open label

If Single-blind, who will be masked?

iv Group Assignment

Parallel

v Study Phase

0

Please specify

vi Study Objectives (Optional)

20 Anticipated trial start date

2017-01-08

21 Target Sample Size

283

22 Recruitment Status

Not Yet Recruiting

23 Primary Outcome

i The Name of the outcome

Volunteering

ii The metric or method of measurement used

Weekly volunteering minutes as measured by the times volunteered per week and duration of volunteering per session

iii The timepoint(s) of primary interest

6 months follow-up

24 Secondary Outcome

i The Name of the outcome

Motivation to volunteer

ii The metric or method of measurement used

Motivation to Volunteer Scale (Grano and Lucidi, 2005)

iii The timepoint(s) of primary interest

6 weeks follow-up

Secondary Outcome

i The Name of the outcome

Positive outcome expectancies towards volunteering

ii The metric or method of measurement used

Expectation Fulfillment Index (Yiu, AU and Tang, 2001)

iii The timepoint(s) of primary interest

6 weeks follow-up

25 Study Information/Publication

i Study Information/Publication Available?

No

ii Link to Study Information/Publication

26 Last Update Date

2018-05-24

27 Primary Registry and Trial Identifying Number

ChiCTR-IIC-17010349

28 Date of Registration in Primary Registry

2016-12-28

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Trial History Detail on 2017-01-16