Primary Healthcare

3

Review clinical trials related to Primary Healthcare. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Exploration of Acceptability of Alcohol Interventions

This is a mixed-methods study consisting of a qualitative assessment the acceptability of psychosocial interventions, delivered by clinical staff. The study will also investigate the correlation between demographic variables and engagement with a North West England, NHS-led, alcohol care service, amongst the patient population.

Participants needed: 2,000
Trial details
Age: 18-67Biological sex: AllType: ObservationalSponsor: East Lancashire Hospitals NHS TrustUpdated: May 12, 2026Locations: 1
Eligibility criteria

Clinical staff who worked in the ELHT alcohol care service, and received trainin... [+1]

Clinical staff who worked in the ELHT alcohol care service, but who no longer wo... [+2]

Status: Not yet recruiting

Nurse-Led Discharge Program and Primary Care Outcomes: A Proof-of-concept Cluster Randomized Controlled Trial

The goal of this cluster randomized controlled trial is to evaluate whether a nurse-led primary health care (PHC) discharge intervention can improve patient activation and primary health care-related outcomes among hospitalized adult patients after discharge.

Participants needed: 120
Trial details
Biological sex: AllType: InterventionalSponsor: The University of Hong KongUpdated: Mar 9, 2026Locations: 1
Eligibility criteria

Hong Kong residents aged ≥18 years [+3]

Having a history of psychiatric/psychological disease or currently on regular ps... [+1]

Status: Recruiting

Evaluation of the Chronic Disease Co-Care Pilot Scheme

The Chronic Disease Co-Care (CDCC) Pilot Scheme is initiated for early screening and management of people with hypertension (HT), pre-diabetes mellitus (pre-DM) and diabetes mellitus (DM) in Hong Kong. This study will evaluate the quality of care, feasibility, acceptability, effectiveness and cost-effectiveness of the Scheme. This is a 12-month cohort study among the District Health Centre (DHC) or DHC Express, healthcare providers, CDCC participants and a comparison group of 1,886 non-participants. All the person-in charge, 2 family doctors and 1 of each allied health provider from each DHC/DHC Express will be administered with the questionnaires on quality of care and costing. All CDCC participants will be included in subject characteristics, among which a convenience sample of 548 will complete a telephone survey on experience, enablement and satisfaction of the CDCC Pilot Scheme. The health outcomes of 1,886 CDCC participants and 1,886 non-participants will be compared for evaluation of effectiveness and cost-effectiveness. Participant characteristics, enablement, compliance to the standards of care, and costing of CDCC Pilot Scheme will be summarized using descriptive statistics. Differences in the proportion of patients meeting treatment targeted for HT, pre-DM and DM after 12 months will be compared by chi-squared test and logistic regressions. The incremental cost-effectiveness ratio will be evaluated by comparing with the World Health Organization (WHO) threshold. This study will inform future healthcare planning and policy for manpower and resource allocation.

Participants needed: 3,772
Trial details
Age: 45+Biological sex: AllType: InterventionalSponsor: The University of Hong KongUpdated: Mar 22, 2024Locations: 1
Eligibility criteria

Hong Kong residents [+4]

With known history of DM or HT [+4]