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Fatigue clinical trials

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NCT ID: NCT00727662 Completed - Breast Cancer Clinical Trials

A Yoga and Wellness Program for Breast Cancer Survivors With Persistent Fatigue

Start date: June 2008
Phase: N/A
Study type: Interventional

This randomized controlled trial will compare the effectiveness of an Iyengar Yoga intervention to a Wellness Seminar health education lecture series, for improvements in energy, mood and biological functioning in breast cancer survivors with persistent, post-treatment fatigue. It is anticipated that the Iyengar Yoga intervention will be feasible and acceptable to breast cancer survivors with minimal side effects and that the Yoga intervention will be effective in improving fatigue and physical performance.

NCT ID: NCT00719563 Completed - Lymphoma Clinical Trials

American Ginseng in Treating Patients With Fatigue Caused by Cancer

Start date: October 2008
Phase: Phase 3
Study type: Interventional

RATIONALE: American ginseng may reduce fatigue in patients with cancer. It is not yet known whether American ginseng is more effective than a placebo in treating cancer-related fatigue. PURPOSE: This randomized phase III trial is studying American ginseng to see how well it works in treating patients with fatigue caused by cancer.

NCT ID: NCT00702637 Completed - Fatigue Clinical Trials

Study of Modafinil to Treat Fatigue in Persons With Traumatic Brain Injury

Start date: October 2002
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine whether Modafinil is effective in: (1) reducing fatigue and excessive daytime sleepiness (EDS) in individuals with Traumatic Brain Injury (TBI); and (2) improving cognitive function and quality of life in individuals with TBI.

NCT ID: NCT00689793 Completed - Fatigue Clinical Trials

Clinical Evaluation of Iron Treatment Efficiency Among Non-anemic But Iron-deficient Female Blood Donors

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Start date: November 2008
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine the subjective response of iron substitution (Tardyferon®) on fatigue in women blood donors with a mean serum ferritin < 30ng/ml and to assess variation of ferritin and hemoglobin after a blood donation.

NCT ID: NCT00683345 Completed - Fatigue Clinical Trials

Fatigue and Interleukin-1 (IL-1) Blockade in Primary Sjøgrens Syndrome

Start date: January 2008
Phase: Phase 2
Study type: Interventional

Fatigue is a prevalent phenomenon in Primary Sjøgrens syndrome (PSS). Observations indicate that the cytokine IL-1 is of importance for this phenomenon. In this study the investigators block IL-1 by giving Anakinra (an IL-1 receptor antagonist) to patients with PSS.

NCT ID: NCT00679809 Completed - Fatigue Clinical Trials

Safety, Fatigue, and Continuity in the Intensive Care Unit (ICU)

Start date: October 2008
Phase: N/A
Study type: Observational

The purpose of this study is to describe the features of continuity and quantify fatigue in three ICU resident work schedules, estimate the frequency of preventable adverse events, and inform the design and demonstrate the feasibility of a future multi-centre study.

NCT ID: NCT00679185 Completed - Breast Cancer Clinical Trials

Expressive Writing in Improving Quality of Life in Patients With Breast Cancer and Lymphedema

Start date: January 2007
Phase: N/A
Study type: Interventional

RATIONALE: Expressive writing may help relieve symptoms and improve quality of life in breast cancer survivors with chronic lymphedema. PURPOSE: This clinical trial is studying expressive writing in improving the quality of life in women with breast cancer and lymphedema.

NCT ID: NCT00677157 Completed - Fatigue Clinical Trials

Evaluation and Diagnosis of People With Pain and Fatigue Syndromes

Start date: May 23, 2008
Phase:
Study type: Observational

This study will examine people who have pain or fatigue symptoms with a known or unknown diagnosis to determine eligibility for other research studies. No treatment is offered under this protocol. People 18 years of age or older with symptoms of pain and fatigue may be eligible for this study. Participants undergo standard examinations needed to diagnose or evaluate their symptoms. The results of the test are used to screen subjects for possible participation in other Nursing Institute studies. The study requires from one to three visits at NIH over 12 months for procedures that may include the following: - Medical history, physical examination and questionnaires related to symptoms and quality of life. - Blood tests - Electrocardiogram - Tender point testing. Pressure is applied to areas of the shoulder, hip, neck, chest, elbow and knee to identify tenderness.

NCT ID: NCT00666614 Completed - Fatigue Clinical Trials

A Pilot Study to Examine Sleep and Fatigue in Pediatric Brain Tumor Patients Hospitalized for High Dose Chemotherapy

Start date: April 2008
Phase: N/A
Study type: Interventional

The purpose of this pilot study is to determine if patients randomized to a hospital sleep environment intervention would have improved sleep quality and reduced fatigue as compared to the patients not receiving the intervention (standard care).

NCT ID: NCT00662103 Completed - Breast Cancer Clinical Trials

Aerobic Exercise, Resistance Exercise, or Flexibility and Relaxation Training in Inactive Older Female Breast Cancer Survivors

Start date: March 2008
Phase: N/A
Study type: Interventional

RATIONALE: Aerobic exercise, resistance exercise, and flexibility and relaxation training may reduce fatigue and improve the health and quality of life of breast cancer survivors. It is not yet known which type of exercise is more effective for inactive older female breast cancer survivors. PURPOSE: This randomized clinical trial is studying aerobic exercise to see how well it works compared with resistance exercise or flexibility and relaxation training in improving the health and quality of life of inactive older female breast cancer survivors.