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
Location
Status: Not yet recruiting

Sleep Hygiene Education in Individuals With Cardiovascular Disease: Effects on Sleep Quality and Disease Management

This clinical trial aims to find out if sleep hygiene education helps people with cardiovascular disease manage their illness better and improve their sleep quality. Participants will be randomly assigned to two groups. One group will receive sleep hygiene education through a 30-minute presentation and twice-daily reminder messages for four weeks. The other group will receive usual care without education. Before and after the four-week period, all participants will complete questionnaires about their sleep habits, sleep quality, and disease management. The study hopes to show that sleep hygiene education can improve participants' sleep and help them manage their disease symptoms better, leading to a better quality of life. The trial will take place at Near East University Hospital's Cardiology Department from June to December 2025.

Participants needed: 100
Trial details
Biological sex: AllType: InterventionalSponsor: Near East University, TurkeyUpdated: Aug 24, 2025
Eligibility criteria

Age 18 years or older [+5]

Pregnancy [+3]

Status: Not yet recruiting

Effect of Pranic Healing on Cardiorespiratory Indices and Pain During Venipuncture in Children

The goal of this clinical trial is to evaluate whether Pranic healing, based on Rogers' therapeutic touch nursing theory, can reduce pain and improve cardiorespiratory indices during venipuncture in children. The main questions it aims to answer are: Does Pranic healing reduce the pain experienced by children during venipuncture? How does Pranic healing affect cardiorespiratory indices, such as heart rate, respiratory rate, and arterial oxygen saturation, during and after venipuncture? Researchers will compare the effects of Pranic healing to routine care (without Pranic healing) to determine its effectiveness. Participants will: Receive Pranic healing or routine care before, during, and after venipuncture Have their pain levels, heart rate, respiratory rate, and arterial oxygen saturation measured Be randomly assigned to either the intervention group (Pranic healing) or the control group (routine care) Have their pain and physiological responses monitored and recorded during the procedure

Participants needed: 46
Trial details
Age: 6-12Biological sex: AllType: InterventionalSponsor: Near East University, TurkeyUpdated: Aug 27, 2024Locations: 1
Eligibility criteria

Children aged 6 to 12 years experiencing pain during venipuncture [+3]

Severe restlessness of the child [+1]