Reminiscence-Based Life Review on Copying With Existential Suffering Among

Status Recruiting

Clinical Trial Summary

Target Issue: Cognitive impairment in older cancer survivors is highly prevalent and the co-existing neuro-psychiatric symptoms, particularly depression, would further complicate the psychosocial consequence of existential suffering. However, no reminiscence-based interventions are specifically developed for older people with cancer have been developed and evaluated. Target Population: Cancer survivors aged 65 years old and above with a mild cognitive impairment identified by the HK-MoCA 5-Min Protocol cognitive assessment. Intervention: This research project aims to implement a brief reminiscence-based intervention that includes six reminiscence chatting sessions among older cancer survivors. The proposed reminiscence-based intervention has great potential to provide psychological and spiritual care as well as comfort to those who are weak, aged and are in need of assistance. Study Objectives: 1. To evaluate the effect of a reminiscence-based life review intervention on copying with existential suffering including meaning of life (primary outcome), cognitive function, psychological distress and social support (secondary outcomes) in older cancer survivors 2. To explore older cancer survivors' experience of the intervention regarding the impact of the intervention on their existential suffering Study Method: The investigator will recruit 116 voluntary elder patients from the outpatient oncology clinics of the Queen Mary Hospital to participate in the study. They will be individually randomized at a 1:1 ratio to receive usual care or the brief reminiscence-based intervention at home. Outcomes will be assessed at baseline (T0), post-intervention (T1), and 6-week follow-up (T2). A qualitative interview regarding the feedback on the intervention will be undertaken only in the intervention group.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05525299
Study type	Interventional
Source	The University of Hong Kong
Contact	Mu-Hsing Ho, PhD
Phone	+852 39102787
Email	mhbho@hku.hk
Status	Recruiting
Phase	N/A
Start date	October 30, 2022
Completion date	August 30, 2024

View Details

See also
Status	Clinical Trial	Phase
Recruiting	`NCT04680611` - Severe Asthma, MepolizumaB and Affect: SAMBA Study
Completed	`NCT05130944` - Feasibility of Community Psychosocial Intervention for Women	N/A
Recruiting	`NCT05526235` - A Scalable Psychological Intervention to Reduce Psychological Distress Among Workers of Assisted Living Facilities	N/A
Recruiting	`NCT05413941` - Internet-based Cognitive Behavioral Therapy in Inflammatory Bowel Disease	N/A
Completed	`NCT03720600` - Forms of Racial Discrimination Study	N/A
Not yet recruiting	`NCT05400096` - Psychological Wellbeing in Clients in Tier 3 Weight Management Service	N/A
Completed	`NCT02212236` - Psychological Intervention for Distress During HSCT	Phase 2
Active, not recruiting	`NCT00892138` - Mindfulness Training for Stress Management	N/A
Recruiting	`NCT04815278` - NC Works4Health: Reducing Chronic Disease Risks in Socioeconomically Disadvantaged, Unemployed Populations	N/A
Recruiting	`NCT04936828` - Ecological Momentary Intervention for Stroke Caregivers' Psychological Support	N/A
Withdrawn	`NCT03341364` - Acceptance and Commitment Based Group Therapy for Cancer Patients	N/A
Recruiting	`NCT05137925` - Mindful Moms: Mechanisms of Mindfulness-based Cognitive Therapy During Pregnancy and Postpartum	N/A
Completed	`NCT04376723` - Mental Health Apps for Mild Psychological Distress Amongst Adolescents	N/A
Active, not recruiting	`NCT04020497` - Ensemble Programme an Early Intervention for Informal Caregivers of Psychiatric Patients	N/A
Not yet recruiting	`NCT03652168` - Stress Free UC Merced: The Effect of 8 Weeks of Mindfulness App Headspace on Stress in a Sample of University Employees	Phase 3
Terminated	`NCT03587896` - Implementation of Self Help Plus in Adult Syrian Refugees in Turkey (RE-DEFINE)	N/A
Completed	`NCT03721770` - Psychological Impact in a Relative, Following the Announcement of the Death of a Loved One After Cardiac Arrest and the Early Request for Organ Donation
Recruiting	`NCT05849454` - Messy Memories: Mobile Application Therapy Following Critical Illness	N/A
Recruiting	`NCT06052904` - Music Breathing for Caregivers of Children Newly Diagnosed With Cancer	N/A
Completed	`NCT04392869` - The Effects of Mindfulness-based Training in Undergraduate Students of Translation and Interpreting	N/A

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

Reminiscence-Based Life Review on Copying With Existential Suffering Among Older Cancer Survivors

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms