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Effects of a web-based decision aid to support decision-making on cervical screening by Chinese working women aged 25–44

Effects of a web-based decision aid to support decision-making on cervical screening by Chinese working women aged 25–44: An exploratory trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN59163820
Enrollment
158
Registered
2022-08-04
Start date
2022-10-01
Completion date
Unknown
Last updated
2025-01-28

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

Conditions

Cervical cancer Cancer

Interventions

Block randomisation with a block size of eight, will be used to allocate eligible participants to the intervention group or the control group in a 1:1 ratio. Randomisation will be performed by a stati

Sponsors

Health and Medical Research Fund
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Current inclusion criteria as of 28/02/2024: 1. Chinese women with a Hong Kong Identity Card 2. Aged =25 and =44 years 3. Engaged in a part-time or full-time job 3. No history of cervical cancer or total hysterectomy 4. A history of sexual activity 5. Able to read or communicate in Chinese or Cantonese 6. No history of a Pap test/HPV DNA testing in their lifetime or no Pap test/HPV DNA testing in the past 3 years 7. Willing to use and have at least one computer, tablet, or smartphone _____ Previous inclusion criteria: 1. Chinese women with a Hong Kong Identity Card 2. Aged =25 and =44 years 3. Engaged in a part-time or full-time job 3. No history of cervical cancer or total hysterectomy 4. A history of sexual activity 5. Able to read or communicate in Chinese or Cantonese 6. No history of a Pap test/HPV DNA testing in their lifetime or no Pap test/HPV DNA testing in the past 5 years 7. Willing to use and have at least one computer, tablet, or smartphone

Exclusion criteria

Exclusion criteria: Cannot read the decision aid by themselves

Design outcomes

Primary

MeasureTime frame
Decisional conflict measured using survey questions at baseline and 2 weeks

Secondary

MeasureTime frame
1. Knowledge about cervical cancer screening measured using survey questions at baseline and 2 weeks 2. Risk perception measured using survey questions at baseline and 2 weeks 3. Clarity of values measured using survey questions at baseline and 2 weeks 4. Screening decision (choice predisposition and choice questions) measured using survey questions at 2 weeks 5. Screening uptake measured using survey questions at 3 months 6. Acceptability of the intervention measured using a telephone interview at 2 weeks

Countries

Hong Kong

Outcome results

None listed

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