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Understanding of the efficacy of recording a diary of things for which one is grateful in the reduction of suffering in terminally-ill patients.

Understanding the efficacy of gratitude journaling in the amelioration of suffering in palliative care patients

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12618001721291
Enrollment
80
Registered
2018-10-18
Start date
2019-01-31
Completion date
2019-12-01
Last updated
2020-07-13

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

Conditions

None listed

Brief summary

Terminally-ill patients always live with physical, psychological, social and/or spiritual sufferring. The purpose of this research is to examine the efficacy of gratitude journaling 3 times a day vs normal journaling 3 times a day in reducing suffering in terminally-ill patients. Research has suggested that expressing the feelings of gratitude may be beneficial to emotional well-being, provides benefits in easing pain and suffering. the hypothesis is gratitude journaling for a week may reduce suffering in palliative care due to enhanced psychosocial functioning.

Interventions

80 adult palliative care patients aged 18 and above will be recruited through random sampling in University Malaya, Malaysia. Patients who are not interested to enroll or confused (according to confusion assessment method) will be excluded from the study. Informed consent will be obtained from all participants. Demographic data of the patients will be collected. All participants will be interview face-to-face by me using Hospital Anxiety and Depression Scale (HADS), GQ-6 form, and the Sufferi

80 adult palliative care patients aged 18 and above will be recruited through random sampling in University Malaya, Malaysia. Patients who are not interested to enroll or confused (according to confusion assessment method) will be excluded from the study. Informed consent will be obtained from all participants. Demographic data of the patients will be collected. All participants will be interview face-to-face by me using Hospital Anxiety and Depression Scale (HADS), GQ-6 form, and the Suffering Pictogram. HADS comprises 14 items, seven of which relate to anxiety symptoms and seven to depressive symptoms. Each item is coded from 0 to 3. The scores for anxiety and depression can therefore vary from 0 to 21, depending on the presence and severity of the symptoms. Baseline score of the scale will be collected. After that, patients will then be randomized and divided into 2 groups – the control group and the intervention group. The control group (normal journaling) will receive standard care, which means they will need to chart the suffering score on Day 1 and Day 7 on the suffering score chart. The suffering score ranges from 0-10 (0 = no suffering, 10 = worst possible suffering). The suffering score will be plotted at the suffering chart. Additionally patients will be required to write down the things that happen around them on a daily basis 3 times a day for 7 days in a diary (provided by me). It can be as simple as news headlines, or a joke you heard from the nurse. The intervention group will receive standard care too, which means they will need to chart the suffering score on Day 1 and Day 7 on the suffering score chart as well. After that, the intervention group will be instructed to keep a diary that record 3 things that they are grateful for on a daily basis for seven days (Gratitude journaling). Participants will be given the following instructions: “For these seven days you are required to write down and record 3 things for which you are grateful on a daily basis. Think back over your day and include anything, no matter small or great, which was a source of gratitude that day. Make the list personal, and try to think of different things each day.” There will not be any specific requirements for the length of the text (how many words or lines written), time spent journaling (minutes per day), or set a daily schedule (e.g., having entries occur in morning or evening). To monitor the adherence, the researcher will pay daily visit to the participant to remind on the diary charting.

Sponsors

tan ting ting
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Diagnosis
Masking
Blinded (masking used) (Subject)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Adult palliative care patients age 18 years old and above will be recruited from University of Malaya Medical Center.

Exclusion criteria

Patients who are not interested to enroll or confused (according to confusion assessment method) will be excluded from the study.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026