Psychometric Properties of the Chinese Version of the Five-item Relationship Satisfaction Scale

February 8, 2023 updated by: Wei XIA, PhD, Sun Yat-sen University
The aims of this study are to translate the five-item relationship satisfaction scale（RS5) into Chinese and assess its psychometric properties among Chinese patients.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

This study will use forward translation, reverse translation, and comprehensive methods to translate the RS5 scale into Chinese ,which will be more in line with the Chinese language and cultural environment. This study will also verify its reliability and validity in a large sample population to form a formal version of the scale. The scale will provide an effective tool for evaluating the degree of relationship satisfaction in China.

Study Type

Observational

Enrollment (Anticipated)

278

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • China
    • Guangdong
      • Guangzhou, Guangdong, China, 510080
        • Recruiting
        • XIAW

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

A total number of 278 spouses/partners who are married or in a romantic relationship.

Description

Inclusion Criteria:

  • ≥18 years old;
  • Participants who are married or in a romantic relationship;
  • Be able to read and communicate in Chinese.

Exclusion Criteria:

  • Those who are unable to communicate due to serious mental or physical illnesses such as deafness, confusion caused by mental illness, etc.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Cohort
  • Time Perspectives: Cross-Sectional

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Questionnaires assessed partners
  1. ≥18 years old;
  2. Participants who are married or in a romantic relationship;
  3. Be able to read and communicate in Chinese.
Other: Questionnaires set
Participants will be asked to respond to the demographic information sheet and the five-item relationship satisfaction scale(RS5) .

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Relationship satisfaction
Time Frame: Baseline
The five-item relationship satisfaction scale（RS5）is a validated self-reported instrument assessing e-cigarette dependence.It consists of five items which are rated on a 6-point Likert scale (1 = Strongly disagree, 6 = Strongly agree).
Baseline

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Sun Yat-sen University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

November 23, 2022

Primary Completion (ANTICIPATED)

August 30, 2023

Study Completion (ANTICIPATED)

October 1, 2023

Study Registration Dates

First Submitted

August 9, 2022

First Submitted That Met QC Criteria

August 9, 2022

First Posted (ACTUAL)

August 10, 2022

Study Record Updates

Last Update Posted (ACTUAL)

February 10, 2023

Last Update Submitted That Met QC Criteria

February 8, 2023

Last Verified

February 1, 2023

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • wjn-RS5

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

The non-identified individual participant data will be shared after the outcomes have been published.

IPD Sharing Time Frame

After the publication of the study

IPD Sharing Access Criteria

Researchers should contact the PI for approval of the study protocol.

IPD Sharing Supporting Information Type

  • SAP

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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