Evaluate the Effectiveness of the Mobile Instant Messaging Intervention
Not Applicable
Not yet recruiting
- Conditions
- Gynecological Cancer
- Registration Number
- NCT06948305
- 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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- Male
- Target Recruitment
- 70
Inclusion Criteria
- 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;
- The spouse has undergone cancer treatment, including surgery, chemotherapy, or radiotherapy;
- Clear consciousness and ability to communicate in Mandarin or Taiwanese;
- Willingness to participate in the study after being informed of the study purpose and procedures.
Exclusion Criteria
Individuals with psychiatric disorders.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Supportive Care Needs -Partners & Caregivers 45, SCNS-P&C45 Post-intervention assessments will be conducted at 1 month, 3 months, and 6 months after the intervention.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Shin Kong Memorial Wu Ho-Su Hospital
🇨🇳Taipei City, Taiwan