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Cultural acceptability and potential effectiveness of dignity therapy for patients with terminal cancer in Taiwan

Cultural acceptability and potential effectiveness of dignity therapy (DT) for patients with terminal cancer in Taiwan: a quasi-experimental study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN99678415
Enrollment
63
Registered
2025-11-11
Start date
2022-04-27
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Cancer dignity-related distress Cancer

Interventions

Participants in the intervention group received a standardized 7-day course of dignity therapy in addition to the standard comfort care provided to the control group. Participants in the control group

Sponsors

National Science and Technology Council
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged 20 years or older 2. Voluntarily agreed to participate 3. Capable of effective communication and completing self-report questionnaires 4. Fluent in either Mandarin Chinese or Taiwanese 5. Diagnosed with terminal cancer with a medically estimated life expectancy of less than six months (added 19/12/2025) Family caregivers in the DT intervention group: 1. Designated by the patient as recipients of the legacy document 2. Aged =20 years 3. Willing to participate 4. Able to communicate effectively 5. Able to complete questionnaires independently. Fluency in Mandarin or Taiwanese is required

Exclusion criteria

Exclusion criteria: 1. Diagnosis of a severe organic brain disorder 2. The presence of a diagnosed mental illness or depression 3. Unconsciousness or cognitive impairment 4. Expected hospital discharge within three days 5. Currently receiving formal palliative care (added 19/12/2025) Family caregivers in the DT intervention group: 1. Caregivers with severe organic brain disorders, mental illness, depression, or cognitive impairment .

Design outcomes

Primary

MeasureTime frame
Dignity-related distress was measured using the Patient Dignity Inventory–Mandarin Version (PDI-MV) at baseline, post-intervention, and two-week follow-up

Secondary

MeasureTime frame
Acceptability was assessed using the Dignity Therapy Patient and Family Feedback Questionnaires (DTPFQ/DTFFQ) at post-intervention

Countries

Taiwan

Contacts

Public ContactLai Wei-Shu
weisue@mail.ncku.edu.tw+886-6-2353535 ext.5821

Outcome results

None listed

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