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Evaluate the Effectiveness of the Mobile Instant Messaging Intervention

Exploring the Care Needs of Spouses of Gynecological Cancer Patients and Evaluating the Development of Care Plans

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06948305
Enrollment
70
Registered
2025-04-29
Start date
2025-08-01
Completion date
2028-07-31
Last updated
2025-04-29

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

Conditions

Gynecological Cancer

Brief summary

This study explores the caregiving needs of male spouses and develops an instant messaging software intervention to provide effective support. The goal is to help male spouses better adjust to their caregiving roles, reduce psychological stress and emotional distress, and improve overall health. A randomized controlled trial will be conducted to evaluate the effectiveness of the mobile instant messaging intervention, analyzing its impact on reducing psychological distress and improving the quality of life of male spouses.

Interventions

BEHAVIORALinstant messaging software

instant messaging software

Sponsors

National Taipei University of Nursing and Health Sciences
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
MALE
Age
18 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

1. Age 18 or older, with a diagnosis of gynecological cancer (including cancers of the cervix, endometrium, fallopian tubes, ovaries, uterus, or vagina), and whose spouse has not been diagnosed with any other type of cancer; 2. The spouse has undergone cancer treatment, including surgery, chemotherapy, or radiotherapy; 3. Clear consciousness and ability to communicate in Mandarin or Taiwanese; 4. Willingness to participate in the study after being informed of the study purpose and procedures.

Exclusion criteria

Individuals with psychiatric disorders.

Design outcomes

Primary

MeasureTime frame
Supportive Care Needs -Partners & Caregivers 45, SCNS-P&C45Post-intervention assessments will be conducted at 1 month, 3 months, and 6 months after the intervention.

Countries

Taiwan

Contacts

Primary ContactHung-Ru Lin, PhD
hungru@ntunhs.edu.tw886-2-2822-7101 Ext. 3197

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026