Clinical trials

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Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
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Status: Not yet recruiting

CEEEC-II: A 12-Week Physical and Cognitive Enrichment Extension Study in Older Stroke Survivors With Multimorbidity

CEEEC-II is a 12-week, community-based, prospective extension study conducted in 32 community health service stations in Kunshan, China. It will invite older stroke survivors with hypertension and/or type 2 diabetes who participated in the preceding CEEEC Phase I trial (NCT06975501) to provide new informed consent and complete Phase II eligibility and baseline assessments. Participants will remain in the physical enrichment, cognitive enrichment, combined enrichment, or usual-care arm assigned to their community cluster in Phase I; no new randomization will occur in CEEEC-II. The upgraded program includes eight physician-led Vitality Camp sessions and four volunteer-led reinforcement activities. The physical component integrates aerobic, resistance, balance, flexibility, Baduanjin, and nutrition education. The cognitive component integrates health education with age-adapted games delivered through an AI-enabled interactive large screen. The primary objective is to evaluate the marginal effect of the cognitive enrichment factor on intrinsic capacity at 12 weeks.

Participants needed: 365
Trial details
Age: 60+Biological sex: AllType: InterventionalSponsor: Duke Kunshan UniversityUpdated: Aug 21, 2026Locations: 1
Eligibility criteria

Completed the endpoint assessment of the preceding CEEEC Phase I trial (NCT06975... [+10]

Life-threatening disease or another condition associated with an expected surviv... [+9]

Status: Recruiting

Comparing Acupuncture With Medication to Reduce Depression, Anxiety and Comorbid Sleep Disorders in China

The main objective of this study is to compare medication (usual care; active comparator) with acupuncture (as experimental intervention) to identify the most (cost)effective and environmentally sustainable intervention to reduce depression, anxiety and comorbid sleep disorders in adults (18-65) in China.

Participants needed: 180
Trial details
Phase: Phase 4Age: 18-65Biological sex: AllType: InterventionalSponsor: Duke Kunshan UniversityUpdated: Jul 29, 2026Locations: 1
Eligibility criteria

Chinese nationals 18-65 years old [+2]

Patients with severe comorbid physical illnesses that prevent them from completi... [+6]

Status: Not yet recruiting

Community-and Primary Care-based Intervention Linked With mObile Technology for HTN Control in Nepal

The clinical trial aims to evaluate whether a community and primary care-based intervention linked with mobile technology (CoPILOT) is acceptable, effective, cost-effective, sustainable, and scalable in improving hypertension (HTN) control among individuals aged 30 to 70 in Nepal. The primary research questions include: Is the use of the application by Frontline Health Workers (FLHWs) and Female Community Health Volunteers (FCHVs) feasible and acceptable? Can FCHVs equipped with mHealth technology effectively increase the linkage of individuals with elevated blood pressure (BP) to health facilities? Does a mobile-based lifestyle intervention reduce or control BP? Can adherence to prescribed HTN treatments be improved among patients through this intervention?

Participants needed: 520
Trial details
Age: 30-70Biological sex: AllType: InterventionalSponsor: Duke Kunshan UniversityUpdated: Aug 17, 2025Locations: 1
Eligibility criteria

Hypertensive patient's should be in the range of 30 to 70 years old living in se... [+4]

Participants who are not able to respond during the data collection period. [+1]

Status: Not yet recruiting

Embedded Community-based Heart-Age Risk Education Trial in Cinese Primary Healthcare

This study evaluates the effectiveness of a brief Heart Age-based risk education intervention embedded in routine primary care for older adults with hypertension in China. The intervention uses routine health check data to generate a personalized one-page Heart Age report, delivered by physicians during regular follow-up visits. The trial tests whether this approach improves risk awareness and self-management behavior without disrupting clinical workflow.

Participants needed: 600
Trial details
Age: 60+Biological sex: AllType: InterventionalSponsor: Duke Kunshan UniversityUpdated: Jul 20, 2025Locations: 1
Eligibility criteria

Adults aged ≥60 years [+3]

Diagnosed dementia or severe cognitive impairment [+2]