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The effectiveness of a sexual health improvement program on sexual function, stress level, and couple relationship in women with gynecologic cancer and their partners

The effectiveness of a sexual health improvement program on sexual function, stress level, and couple relationship in women with gynecologic cancer and their partners

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
TCTR
Registry ID
TCTR20251124006
Enrollment
100
Registered
2025-11-24
Start date
2026-02-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Women with a newly diagnosed gynecologic cancer who have gynecologic cancer in stage I, II, III. They are receiving all treatments and their partners. gynecologic cancer, sexual health, sexual function, stress level, and couple relationship, partner, after treatments

Interventions

Routine care is the activities provided for patients with gynecologic cancer and their partners who receive services at the gynecologic outpatient department (OPD) and gynecologic ward of the National
s central region. These activities are carried out by ward nurses, who provide essential post-treatment care instructions, along with an informational pamphlet on post-treatment care. For example, sur
2) Sexual Health Information
3) Self-Awareness and Health Care through Exercise
4) Letting go and focusing on sensation in the present
5) Reflect on their relationship and share responsibilities
6) Good conv
No Intervention No treatment,Experimental Behavioral
Routine,The sexual health improvement program

Sponsors

Suphatida Chanburee, Principal Investigator
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: The women will be recruited for the study as follows: 1) Women aged 18 years and over who have signed an informed consent form. 2) Women with a newly diagnosed gynecologic cancer who have gynecologic cancer in stage I, II, III. They are receiving all treatments. 3) In the case of patients who have undergone surgery, they must wait at least 6 weeks after the procedure as it is recommended to avoid sexual activity during this period of time. 4) Women living with a male heterosexual partner. 5) Women with a total FSFI of less than 23.10, which is defined as sexual dysfunction. (Chongcharoen et al., 2024) 6) Women are conscious with normal vision, hearing, understand Thai language, and has the ability to answer questionnaires. 7) Women obtain mobile phones or computer with access to the internet. The partners will be recruited for the study as follows: 1) Partners aged 18 years and over who have signed an informed consent form. 2) The partner is male and sexually active with the female participant. 3) Partners are conscious with normal vision, hearing, understand Thai language, and can answer questionnaires. 4) Partners obtain mobile phones or computer with access to the internet.

Exclusion criteria

Exclusion criteria: Exclusion Criteria for Female Participants: 1) Women with severe psychiatric history or on psychiatric medication. 2) Women with serious physical illnesses (e.g. severe heart disease, neurological disorders, active STIs). 3) Women whose male partners do not participate or withdraw early. Exclusion Criteria for Male Partners: 1) Men with severe psychiatric history or on psychiatric medication. 2) Men with severe erectile dysfunction (IIEF-5 score < 8) before participation.

Design outcomes

Primary

MeasureTime frame
Sexual function Baseline, immediately post-intervention, 1-month and 3-month follow-up The Thai Female Sexual Function Index (FSFI) for women and The Thai International Index of Erectile Function (IIEF-5) for male partners

Secondary

MeasureTime frame
Stress level Baseline, immediately post-intervention, 1-month and 3-month follow-up The Thai Perceived Stress Scale-10 (T-PSS-10) for women and their partners.,Couple relationship Baseline, immediately post-intervention, 1-month and 3-month follow-up The Thai version of the Dyadic Adjustment Scale (DAS) for women and their partners.

Countries

Thailand

Contacts

Public ContactSuphatida Chanburee

Faculty of Nursing, Thammasat University

Suphatida.cha@gmail.com0936468995

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026