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NCT ID: NCT06226285 Not yet recruiting - Quality of Life Clinical Trials

Quality of Life for Carers Through a Person-Centred Technological Solution

TechQoL4Carers
Start date: April 1, 2024
Phase: N/A
Study type: Interventional

This study is entitled Quality of Life for Carers through a Person-Centred Technological Solution, whose acronym is TechQoL4Carers. The goal of this pilot study is to develop an innovative technological solution (TechQoL4Carers) to improve the Quality of Life (QoL), occupational balance, impact of care, self-management of health, and empowerment of informal caregivers of older people or people with disability. The main question it aims to answer is: Will the routine use of TechQoL4Carers platform have a positive impact on the daily life of informal caregivers? The study will examine these variables in a specific way: QoL, impact of care and burden, occupational balance, health self-management, and empowerment. Informal caregivers will participate in a participatory process of development, testing and validation of the technological platform TechQoL4Carers. At the beginning and end of the study, participants will be asked to answer questionnaires to capture their perspective on the central variables of the study and on the utility and usability of the technology. Then, for three months, participants will: - use TechQoL4Carers platform on their mobile phone or computer, - wear the Xiaomi Smart Band 7/8, - provide weekly reports of health and care related quality of life, - and receive personalized recommendations and training materials. At the end, they will also participate in an in-depth interview on the impact of the project on their daily activities.

NCT ID: NCT06146868 Not yet recruiting - Technology Clinical Trials

Gerontechnology Evaluation Framework: Outcome Validation

Start date: November 2023
Phase:
Study type: Observational

The project aims to validate the evaluation indicators applicability of 9 Gerontechnology Evaluation Frameworks. The outcome is the perceived importance of the evaluation indicators described in the 9 Evaluation Frameworks. Participants will be invited to complete a questionnaire indicating the importance of the outcomes.

NCT ID: NCT04634851 Not yet recruiting - Diet Habit Clinical Trials

Video Home Visits for Dietary Counselling

Start date: July 1, 2027
Phase: N/A
Study type: Interventional

This pilot study aims to develop a protocol for home video informed dietary counseling with the goal of reducing overall sodium consumption among kidney stone formers. To accomplish this the investigators will: 1)Assess which data available on video visits are most informative to convey patient sodium consumption, and 2) Administer virtual home visits with informed dietary counseling in our intervention arm and compare this to standard dietary counseling looking specifically at the outcome of 24-hour urine sodium excretion results over time. This study will benefit dramatically from the rapid growth of telehealth medical visits as a consequence of the SARS-CoV-2 pandemic, with the ultimate goal to improve and adapt patient dietary counseling for the prevention of kidney stone disease in the new and evolving era of telehealth.

NCT ID: NCT03597984 Not yet recruiting - Radiotherapy Clinical Trials

Reduction of Pain Symptoms With Stereotactic Radiotherapy on Bone Metastases

PREST
Start date: July 1, 2019
Phase: N/A
Study type: Interventional

Interventional study without medicinal, randomized 1: 1 open-label, multicenter, phase 3 to evaluate the response in terms of reduction of pain symptomatology from bone metastases, comparing the conformational radiotherapy (3D-CRT) administered in conventional fractionation vs. extracranial stereotactic radiotherapy (SBRT) administered with concomitant integrated simultaneous boost (Simultaneous Integrated Boost-SIB)

NCT ID: NCT03554135 Not yet recruiting - Radiotherapy Clinical Trials

Single frActIoN eighT Gray Palliative Radiotherapy With Modulated Intensity for Pain Reduction

SAINT
Start date: December 1, 2018
Phase:
Study type: Observational [Patient Registry]

Non-randomized, monocentric, observational study to evaluate the response in terms of reduction of painful symptoms from bone metastases to radiotherapy with high personalization of treatment: performed with modern technology, supplied with modulated intensity technique with concomitant integrated boost, according to selection of patients in accordance with prognosis determined by specific prognostic score