The Effects of a Health-social Partnership Program for Discharged Non-frail Older Adults
1 other identifier
interventional
75
1 country
1
Brief Summary
Previous studies supporting discharged patients are hospital-based which admission criteria tend to include mainly those with complex needs and/or specific disease conditions. This study captured the service gap where these non-frail older patients might have no specific medical problem upon discharge but they might encounter residual health and social issues when returning home.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Jun 2017
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 19, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 30, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
April 30, 2020
CompletedFirst Submitted
Initial submission to the registry
June 11, 2020
CompletedFirst Posted
Study publicly available on registry
June 17, 2020
CompletedJune 17, 2020
June 1, 2020
2.9 years
June 11, 2020
June 13, 2020
Conditions
Outcome Measures
Primary Outcomes (1)
Change from baseline Health-related quality of life: SF-12 at 3 months
The goal for this program was to enable older adults to live with optimum quality of life in their own environment through receiving support from the collaboration of nurse case managers and social workers. Quality of life was measured by SF-12, which has been shown to be useful in Chinese elderly patients. The questionnaire has 12 items organized into eight categories (physical functioning, role limitation due to emotional and physical problems, mental health scale, general health, bodily pain, social functioning, and vitality), and has been validated in numerous studies.
At baseline pre-intervention and at three months when the interventions were completed.
Secondary Outcomes (3)
Change from baseline Activity of daily living at 3 months
At baseline pre-intervention and at three months when the interventions were completed.
Change from baseline Presence of depressive symptoms at 3 months
At baseline pre-intervention and at three months when the interventions were completed.
Change from Total number of unplanned outpatient department, general practitioner, and emergency department visits, hospital admissions and total number of health service attendances at 3 months
At baseline pre-intervention and at three months when the interventions were completed.
Study Arms (2)
Intervention group
EXPERIMENTALThe subjects in this group receive complex interventions, including structured assessment, health education, goal empowerment, and care coordination supported by a health-social team.
Control group
OTHERThe control group received usual discharge care and community resources that were made available to them as appropriate. A monthly social call was made to each client in the control group in order to exclude social effects. The contents of the social call, such as asking about entertainment and clients' hobbies, were set in the protocol.
Interventions
An advanced practice nurse (APN) from a hospital discharge team visited them to familiarize him/herself with their condition and prepare a discharge plan. A face-to-face or telephone call handover between the APN and the project nurse case manager (NCM) was performed before the client was discharged. The past and current medical conditions, medical and nursing management, and follow-up appointments were discussed. After discharge home, the NCM, functioning as the leader of health-social care team, conducted the initial assessment in the first home visit to identify the client's health and social problems within one week of discharge. Community workers, supervised by both the nurse case manager and social worker, provided telephone follow-up and subsequent home visits to monitor the client's progress and provide support when necessary.
Eligibility Criteria
You may qualify if:
- resided in the service areas of the study hospital,
- were aged 60 or over,
- were cognitively competent with a score greater than 26 in the Montreal Cognitive Assessment Hong Kong version,
- were living at home before and after discharge from the hospital,
- had scores of \<5 on the Clinical Frailty Scale (Note: a patient is considered to be non-frail if they have a score less than 5), and
- were fit for medical discharge
You may not qualify if:
- were not able to communicate,
- could not be reached by phone,
- were bed-bound,
- had active psychiatric problems,
- were already engaged in other structured health or social programs, and
- would not be staying in Hong Kong for the three months of the study
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- The Hong Kong Polytechnic Universitylead
- The Queen Elizabeth Hospitalcollaborator
Study Sites (1)
Queen Elizabeth Hospital
Kowloon, Hong Kong
Related Publications (1)
Wong AKC, Wong FKY, Ngai JSC, Hung SYK, Li WC. Effectiveness of a health-social partnership program for discharged non-frail older adults: a pilot study. BMC Geriatr. 2020 Sep 10;20(1):339. doi: 10.1186/s12877-020-01722-5.
PMID: 32912218DERIVED
Study Officials
- PRINCIPAL INVESTIGATOR
Arkers KC Wong, Dr
The Hong Kong Polytechnic University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Clinical associate
Study Record Dates
First Submitted
June 11, 2020
First Posted
June 17, 2020
Study Start
June 19, 2017
Primary Completion
April 30, 2020
Study Completion
April 30, 2020
Last Updated
June 17, 2020
Record last verified: 2020-06
Data Sharing
- IPD Sharing
- Will not share
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.