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Fatigue clinical trials

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NCT ID: NCT00335491 Completed - Breast Cancer Clinical Trials

Exercise in Improving Mobility and Reducing Fatigue and/or Weakness in Older Cancer Survivors

Start date: March 2006
Phase: N/A
Study type: Interventional

RATIONALE: Exercise may help improve mobility and relieve fatigue and/or weakness in cancer survivors. It is not yet known whether exercise is more effective than standard therapy in improving mobility and reducing fatigue and/or weakness in older cancer survivors. PURPOSE: This randomized clinical trial is studying exercise to see how well it works compared to standard therapy in improving mobility and reducing fatigue and/or weakness in older cancer survivors.

NCT ID: NCT00321880 Completed - Leukemia Clinical Trials

Healing Touch in Treating Patients Receiving Chemotherapy for Acute Myeloid Leukemia or Acute Lymphocytic Leukemia

Start date: February 2006
Phase: N/A
Study type: Interventional

RATIONALE: Supportive care, such as healing touch, may improve quality of life in patients receiving chemotherapy for acute leukemia. PURPOSE: This clinical trial is studying how well healing touch works in treating patients receiving chemotherapy for acute myeloid leukemia or acute lymphocytic leukemia.

NCT ID: NCT00292578 Completed - Fatigue Clinical Trials

NAET® Testing Devices in Detection of Hypersensitivity to Cane Sugar

Start date: January 2005
Phase: Phase 1/Phase 2
Study type: Interventional

Background: Studies have noted a correlation between food sensitivities and health disorders. Various commonly seen health problems may be caused by cane sugar since it is lavishly and frequently used by people worldwide. Objective: This study evaluated the efficacy of NAET testing instruments in detecting hypersensitivities to cane sugar. Materials and Methods: Seventy-four subjects volunteered for this study. They were asked to write down one of their major health problems, the amount of sugar consumed on a daily basis and any known health problem(s) related to sugar consumption. The following testing modalities were used in the study: (1). Allergy Symptom-Rating Scale (ASRS); (2). NST Rating Scale (NSTRS); (3). Pulse Difference Rating Scale (PDRS). Test-1 was done twice. Tests 2 and 3 were done three times each: once without contacting sugar and then contacting sugar at one minute and ten minutes.

NCT ID: NCT00288795 Completed - Fatigue Clinical Trials

A Randomized Study of Polarity or Massage Therapy to Reduce Fatigue in Breast Cancer Patients During Radiation Therapy

Start date: January 2006
Phase: Phase 1/Phase 2
Study type: Interventional

This research study is being conducted to compare the effectiveness of two types of complimentary medicine treatments to see if they will reduce the fatigue experienced by breast cancer patients receiving radiation therapy. The treatments being studied are Polarity Therapy and Massage Therapy. The primary study hypothesis is that Polarity Therapy will be efficacious in relieving fatigue in breast cancer patients receiving radiation treatments. The secondary hypothesis is that Polarity Therapy will be efficacious in improving health-related quality of life in breast cancer patients receiving radiation treatments.

NCT ID: NCT00273208 Completed - Clinical trials for Fatigue After Adjuvant Breast Cancer Treatment

An Intervention to Decrease Fatigue Among Breast Cancer Survivors

Start date: September 2005
Phase: N/A
Study type: Interventional

This research project is being done to design and then test whether a 10 week program can help reduce the symptoms of being tired and fatigued among women who have had breast cancer. The pilot study will include 4 groups of women, two groups of women from Baltimore and two groups of women from Washington County, Maryland. Each group will have 5 to 6 women. The purpose of this pilot study is to help us find the best things to include in the program to help women who have had breast cancer and who have severe problems with fatigue that has lasted months to years after being treated with chemotherapy or radiation therapy. Following the pilot program we will conduct and evaluate (using a quasi-experimental design comparing fatigue scores before and after the intervention) the efficacy of the refined 10-week integrated mind/body medicine approach to reduce symptoms of fatigue among breast cancer survivors who have completed their adjuvant therapy. Four intervention groups (~12 women per group) will be conducted: two in the urban setting and two in the rural setting. We will assess fatigue symptoms at baseline, immediately after the program, 2 months and 6 months following completion of the program. We will compare mean baseline scores to post-intervention scores. The ultimate goal is to develop a non-pharmacologic, holistic, low risk intervention for improving symptoms of fatigue and thus improving quality of life among breast cancer survivors

NCT ID: NCT00268502 Completed - Breast Cancer Clinical Trials

Quality of Life in African-American or Caucasian Female Breast Cancer Survivors

Start date: December 2005
Phase: N/A
Study type: Observational

RATIONALE: Studying quality of life in cancer survivors may help determine the long-term effects of breast cancer and may help improve the quality of life for future cancer survivors. PURPOSE: This clinical trial is studying the quality of life in African-American or Caucasian female breast cancer survivors.

NCT ID: NCT00233090 Completed - Fatigue Clinical Trials

Post-Traumatic Brain Injury (Post-TBI) Fatigue and Its Treatment

Start date: July 2005
Phase: Phase 2
Study type: Interventional

Randomized clinical trial of modafinil vs. placebo for treatment of fatigue after TBI.

NCT ID: NCT00215800 Completed - Clinical trials for Chronic Fatigue Syndrome

The Study of the Safety and Efficacy of Ampligen in Chronic Fatigue Syndrome

Start date: December 1998
Phase: Phase 3
Study type: Interventional

multi-center, double-blind, randomized, placebo-controlled study of the safety and efficacy.

NCT ID: NCT00188331 Completed - Fatigue Clinical Trials

Cognitive Function and Fatigue in Colorectal Cancer (CRC) Patients After Chemotherapy

Start date: November 2003
Phase: N/A
Study type: Observational

This is a prospective, longitudinal cohort study to evaluate fatigue and cognitive function in patients with colorectal cancer (CRC) treated with chemotherapy, and in patients with the same malignancy, that do not receive chemotherapy. A self-report questionnaire for fatigue (the FACT-F), and validated tests of cognitive function, will be applied at predetermined times before, during and after chemotherapy, to determine the incidence, severity and duration of these symptoms. Comparisons will be made in changes in cognition for individuals, as well as between the chemotherapy and the control group. Mechanisms that might lead to fatigue and/or cognitive decline will be investigated.

NCT ID: NCT00182780 Completed - Fatigue Clinical Trials

American Ginseng in Treating Patients With Cancer-Related Fatigue

Start date: October 2005
Phase: N/A
Study type: Interventional

RATIONALE: American ginseng may help relieve cancer-related fatigue. PURPOSE: This clinical trial is studying how well American ginseng works in treating patients with cancer-related fatigue.