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Improve Quality of Life clinical trials

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NCT ID: NCT04761367 Recruiting - Clinical trials for Improve Quality of Life

Exercise Program After Total Hip and Knee Replacement: a Randomized Controlled Trial

PAIR
Start date: January 1, 2021
Phase: N/A
Study type: Interventional

Randomized controlled trial. Patients will be enrolled at the moment of the pre-surgery assessment after verifying the inclusion/exclusion criteria and signing written informed consent. After surgical treatment (THR or TKR) and subsequent rehabilitation treatment (which usually lasts 3-4 months) patients will be contacted and the persistence of inclusion/exclusion criteria verified again. For each type of surgical procedure (i.e. THR or TKR) those, with confirmed inclusion criteria will be randomly assigned to the IG or the CG. The IG will participate in a 6-month exercise program based on the PAIR exercise protocol and will receive educational sessions and material on the importance of maintaining an active life style after THR or TKR. The CG will receive only educational sessions and material on the importance of maintaining an active life style after THR or TKR. Participants of both IG and CG will be assessed at the moment of randomization (post-surgery baseline) and, subsequently, after 3 and 6 months.

NCT ID: NCT02943655 Completed - Clinical trials for Heavy Menstrual Bleeding

Treatment of Heavy and/or Prolonged Menstrual Bleeding Without Organic Cause

Start date: November 1, 2017
Phase: Phase 3
Study type: Interventional

Abnormal uterine bleeding encompasses abnormalities in the regularity, duration of flow, frequency, and/or blood flow volume relative to normal menstruation. Of these menstrual abnormalities, heavy menstrual bleeding (HMB), defined objectively as a blood loss of 80 ml or more per menstrual cycle , which is unrelated to pregnancy or known pelvic or systemic disease.

NCT ID: NCT00639210 Completed - Clinical trials for Improve Quality of Life

BREAST CANCER AND EXERCISE

BREX
Start date: September 2005
Phase: Phase 3
Study type: Interventional

A Finnish Breast Cancer Group Study (BREX 01-2004). A multicenter phase III open randomised trial of the efficacy of exercise in the prevention of long-term adverse effects of adjuvant treatments and breast cancer recurrences in women with primary breast cancer. The aim of the study is to investigate whether regular exercise training could reduce the long-term side effects of adjuvant treatments of primary breast cancer and improve quality of life and well being.