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Psycho-educational interventions for gynecological cancer patients

A randomized controlled trial of psycho-educational interventions for reducing uncertainty and anxiety, and improving sexual functioning among gynecological cancer patients in Hong Kong

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN21846801
Enrollment
200
Registered
2016-09-08
Start date
2016-09-09
Completion date
Unknown
Last updated
2020-02-24

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

Conditions

Gynecological cancer Cancer Gynecological cancer

Interventions

The participants will be assigned randomly to participate in a psycho-educational intervention program or to an attention control group: Psycho-educational intervention group: Partici

Sponsors

Food and Health Bureau, The Government of the Hong Kong Special Administrative Region
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Women with a new diagnosis of primary gynecological cancer including uterine, ovarian and cervical cancers over the past three months 2. Planning for surgery as the first-line treatment 3. Older than 18 years 4. Able to understand spoken Cantonese and to read all materials printed in Chinese 5. Able to consent to participate

Exclusion criteria

Exclusion criteria: Patients with known psychiatric morbidity.

Design outcomes

Primary

MeasureTime frame
Level of uncertainty will be measured using the Chinese version of Mishel Uncertainty in Illness Scale (C-MUIS) at baseline and the completion of the intervention (3-4 months).

Secondary

MeasureTime frame
1. Level of anxiety will be measured using the Chinese version of the anxiety subscale in the Hospital Anxiety and Depression Scale (HADS) at baseline and the completion of the intervention (3-4 months) 2. Sexual functioning will be measured using the Chinese version of Sexual Function-Vaginal Changes Questionnaire (SVQ) at the completion of the intervention (3-4 months)

Countries

Hong Kong

Outcome results

None listed

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