Symptom

3

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

Condition / disease
Location
Status: Not yet recruiting

Symptom Severity, Posture, Pain, and Physical Activity in Gastroesophageal Reflux Disease

This study is a cross-sectional research designed to investigate symptom severity, posture, musculoskeletal pain, and physical activity levels in individuals with gastroesophageal reflux disease (GERD).

Participants needed: 51
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Karabuk UniversityUpdated: Jun 15, 2026
Eligibility criteria

Being diagnosed with gastroesophageal reflux disease (GERD) [+2]

Presence of a diagnosed psychiatric disorder [+1]

Status: Recruiting

Mindfulness Meditation in Hemodialysis Patients

This randomised controlled study aims to evaluate the effects of mindfulness meditation on sleep quality, perceived stress and symptoms levels ion hemodialysis patients. Participants in the intervention group will receive a 4 week mindfulness meditation program in addition to routine care. Outcomes will be assessed before and after the intervention using validated measurement tools.

Participants needed: 50
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Cyprus Aydin UniversityUpdated: Jun 2, 2026Locations: 4
Eligibility criteria

Patients aged between 18 and 75 years [+7]

Patients younger than 18 years or older than 75 years [+7]

Status: Not yet recruiting

Advanced Symptom Palliation Through Integrated Relief Engagement

Beacon is a digital platform that processes objective and subjective aggregated data provided by patients. Objective data is provided by standard wearables, while subjective data is provided by patient-reported outcome measures (PROMs), comprising written and vocal patient reporting. The ASPIRE.AI study is a prospective study evaluating the feasibility of clinicians' use of aggregated data that was provided by patients and analyzed through "Beacon", and its influence on advanced cancer patients' palliative symptoms management. Approximately 40 consecutive eligible ambulatory advanced cancer patients first attending the palliative unit in the Davidoff Center will be enrolled. The trial will continue for \~1 year, with each patient participating in this trial for a total of about 12 weeks. All participants will receive the intervention. The intervention comprises the palliative standard of care treatment along with the usage of the Beacon digital platform, which enables comprehensive data collection and aggregation regarding the patient's biopsychosocial status, and thus, the patient's symptom burden. Data collected and aggregated through Beacon includes Beacon data provided by the patients via wearables (smartwatch/sensors), smartphones, and written and recorded PROMs. Researchers will then evaluate physician engagement with the platform, Influence on treatment, and the physician user experience rating as well as patients' adherence, satisfaction with Beacon usage, and changes in patients' symptom burden and quality of life.

Participants needed: 40
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Tzeela CohenUpdated: Apr 9, 2026Locations: 1
Eligibility criteria

Outpatients treated and followed at the Davidoff Center [+8]

Patient without active disease [+6]