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NCT Number: NCT06559917

Effectiveness on Family Cohesion and Happiness of Using Social Media to Enhance Happiness Accounts for Late-Stage Cancer Patients and Their Families

The study period is from September 1, 2024, to December 31, 2025. The subjects are cancer patients from the medical center of this hospital. A block randomization will be used to assign 100 patients to the experimental group and 100 patients to the control group, totaling 200 patients. During the study process, questionnaires and medical records of the subjects will be collected. The experimental group will receive the social media "Happiness Ledger" intervention, while the control group will receive routine treatment. Questionnaires will be collected from both groups before and after the intervention.

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Key information

Conditions

Age range

20 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

-

Inclusion criteria

for Advanced Cancer Patients:

  • Patients diagnosed with stage III or IV cancer by a specialist physician.
  • Patients who agree to participate in the study after being informed about the research.
  • Patients who are conscious and able to communicate in Mandarin or Taiwanese.
  • Patients aged 20 years or older.
  • Patients with no history of mental illness.

Inclusion criteria

for Family Members:

  • The primary caregiver of a patient diagnosed with stage III or IV cancer by a specialist physician.
  • The primary caregiver who has a blood, marital, or cohabitation relationship with the patient.
  • Family members who agree to participate in the study after being informed about the research.
  • Family members who are conscious and able to communicate in Mandarin or Taiwanese.
  • Family members aged 20 years or older.
  • Family members with no history of mental illness.

Exclusion criteria

-

Exclusion criteria

for Advanced Cancer Patients:

  • Patients in the experimental group and control group who reside in the same ward.
  • Patients who share a ward with subjects already included in the study.
  • Patients involved in ongoing medical disputes.
  • Patients who cannot understand the study explanation due to language or cognitive impairments.
  • Patients with a life expectancy shorter than the planned study duration.

Exclusion criteria

for Family Members:

  • Family members who do not have direct living or caregiving contact with the patient.
  • Family members who cannot visit the patient regularly or participate in the study.
  • Family members who cannot understand the study explanation due to language or cognitive impairments.
  • Family members with significant visual or hearing impairments who do not use assistive devices and cannot resolve communication issues.
  • Family members who cannot make independent decisions.

Treatment and study plan

life review

Other

After consenting, they will complete the first questionnaire before receiving the "Happiness Ledger" intervention via social media. Family members will have one week to organize photos, after which patients will share the meaning of the photos. This process will be recorded by the researcher and will last approximately 40 to 60 minutes. The researcher will then create a three-minute video using the photos, and the participating family members will assist in uploading the photos to the family LINE group as feedback to the subjects. The second questionnaire will then be completed.

Primary outcomes

  1. Family Cohesion

    Time frame: Baseline (pre-intervention) and 1 week after intervention

    This study uses the Family Adaptability and Cohesion Evaluation Scale (FACES II) developed by Olson et al. (1979), which consists of 30 items to measure the family cohesion of patients and their families .

Secondary outcomes

  1. Happiness

    Time frame: Baseline and 1 week

    This study uses the Subjective Happiness Scale (SHS) created by Lyubomirsky & Lepper (1999), which consists of 4 items to measure the happiness of patients and their families."

Sponsors and collaborators

Lead sponsor

YANG WEN-CHI

Other

Registry information

Important dates

Study start
2024
Primary completion
2024
Study completion
2025
First posted
Aug 19, 2024
Registry last updated
Aug 19, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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