Telephone-delivered lifestyle support with action planning and motivational interviewing techniques to improve rehabilitation outcomes.
Andrea Döbler, Bea Herbeck Belnap, Hartmut Pollmann...
https://pubmed.ncbi.nlm.nih.gov/29878825/Actively Recruiting
Led by The University of Hong Kong · Updated on 2025-03-30
270
Participants Needed
1
Research Sites
N/A
Total Duration
Researchers are studying ways to help older adults, aged 70 years and above, make informed decisions about receiving recommended vaccines, including seasonal influenza, pneumococcal, and possibly annual COVID-19 vaccines. The study aims to improve older peoples confidence, self-efficacy, emotional engagement, and positive future outlook to increase vaccination uptake. This trial is a randomized controlled study focusing on community-dwelling older people and uses the Mental Models Approach and Patient Activation Approach to design interventions. The study compares two groups an intervention group receiving a specially designed booklet and six weekly telephone sessions using motivational interviewing techniques to activate patient engagement, and a control group receiving a pamphlet with vaccine recommendations plus six short telephone calls offering general health advice. The booklet is crafted to address older adults mental models and emotional decision-making preferences, while the telephone sessions aim to support knowledge, skills, and confidence in vaccination decisions. Participants will be involved in baseline questionnaires and follow-up assessments at one and four months after the interventions to track vaccination uptake and changes in attitudes, knowledge, emotions, and behaviors. Data will be collected through questionnaires and telephone interviews, and outcomes like vaccine uptake rates and patient activation measures will be analyzed. The study includes careful monitoring to ensure participant understanding and consent, with data handled securely and anonymously throughout the trial.
CONDITIONS
Older People's Preventive Care Utilization
Q
Qiuyan Liao
Y
Yuyi Chen
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The University of Hong Kong
Lead Sponsor
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (phone-based screening and baseline assessment)
Duration - 6 weeks
Participants in the intervention group receive a booklet designed to support preventive care decision-making and six telephone-based patient activation sessions over six weeks to promote vaccination uptake and self-management skills.
6 telephone sessions, each around 20 minutes
Duration - 6 weeks
Participants in the control group receive a pamphlet about recommended vaccinations and six control telephone care visits over six weeks focusing on general health advice.
6 telephone visits, each around 5 to 10 minutes
Duration - 4 months
Participants complete follow-up assessments within 1 month and again at 4 months after the intervention to measure vaccination uptake and changes in health behaviors and attitudes.
2 follow-up assessments (within 1 month and at 4 months post-intervention)
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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Lead Sponsor