Patient Empowerment

3

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

Condition / disease
Location
Status: Recruiting

Perineal Massage Using A Pelvic Wand During Pregnancy

There is limited research on the optimal strategy to reduce obstetric laceration, postpartum urinary retention, and postpartum pelvic pain. In systematic reviews, clinician-directed massage of the perineal muscles at the time of birth and patient directed massage of the perineal muscles in the third trimester to inconsistently reduce the incidence of severe obstetric laceration.1,2 However, there is significant heterogeneity of these studies is due in large part to the lack of a standardized protocols and unpredictability of clinician availability to perform perineal massage around the time of birth. The purpose of this study is to understand how perineal massage with a pelvic wand in late pregnancy and during labor influences one's sense of self-control over the labor process and birth experience.

Participants needed: 140
Trial details
Phase: Phase 4Age: 18+Biological sex: FemaleType: InterventionalSponsor: Beth Israel Deaconess Medical CenterUpdated: Mar 9, 2026Locations: 1
Eligibility criteria

Pregnant [+4]

Contraindication to vaginal birth, active genital herpes infection, fetal anomal...

Status: Not yet recruiting

Management of Chronic Non-Cancer Pain With Non-Pharmacological Therapies

A randomized controlled clinical trial will be conducted, involving a psychoeducational activity as the intervention. There will be a control group of patients with non-cancer chronic pain who will continue their usual treatment. The trial will end after 3 months. Pain, well-being, medication management, mood, self-esteem, and quality of life will be compared just before starting the workshop with the status at the end of the workshop (one month later) to assess the immediate effect, and three months later to evaluate the medium-term effect. These measurements will be taken in both the control and intervention groups. Additionally, for the intervention group, a follow-up will be conducted six months after the workshop ends to assess the long-term effect duration. This study does not allow blinding of patients or professionals conducting the intervention, but the person analyzing the data to compare the effect produced in the control and intervention groups will be blinded. Therefore, it is an observer-blind evaluation.

Participants needed: 128
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Hospital San Juan de Dios del Aljarafe de SevillaUpdated: Jun 5, 2024Locations: 1
Eligibility criteria

Patients aged 18 years or older, [+4]

Patients in the diagnostic phase, [+3]

Status: Not yet recruiting

Urinary Proteomics Combined With Home Blood Pressure Telemonitoring for Health Care Reform

UPRIGHT-HTM will compare risk stratification, treatment efficiency and health economic outcomes of a diagnostic approach based on home blood pressure telemonitoring combined with urinary proteomic profiling with home blood pressure telemonitoring alone

Participants needed: 1,000
Trial details
Age: 55-75Biological sex: AllType: InterventionalSponsor: KU LeuvenUpdated: Mar 6, 2020Locations: 12
Eligibility criteria

Patients must have at least three additional guideline-defined risk factors, pre... [+3]

Type 1 diabetes mellitus; [+7]