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Spots Global Cancer Trial Database for Meditation Therapy in Improving Anxiety and Depression in Cancer Patients With Psychosocial Distress

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Meditation Therapy in Improving Anxiety and Depression in Cancer Patients With Psychosocial Distress

Official Title: Self-Administered Meditation Intervention for Cancer Patients With Psychosocial Distress

Study ID: NCT02988271

Study Description

Brief Summary: This trial studies how well self-administered meditation therapy works in improving anxiety and depression in cancer patients who exhibit psychosocial distress. Meditation therapy is a mind-body approach that uses a variety of techniques, such as deep breathing, sound, or movement, that may help to decrease distress and anxiety and enhance the health and quality of life of patients with cancer.

Detailed Description: PRIMARY OBJECTIVES: I. To determine the feasibility of having patients self-administer meditation recordings using a portable, computer-based program during a 2-week period. SECONDARY OBJECTIVES: I. Assess the effect of self-administered meditation on anxiety, depression and other symptoms that are part of the Edmonton Symptom Assessment Scale (ESAS) questionnaire. II. Evaluate participant satisfaction with the meditation delivery and tracking program. III. Examine the association between the frequency of practice (number of sessions a day) and choice of length of practice (5, 10, or 15 minute sessions) and anxiety, depression and other patient reported outcomes. OUTLINE: Patients are randomized to 1 of 2 groups. GROUP I (MEDITATION): Patients watch a pre-recorded instructional meditation video via an iPod meditation app. Patients then complete meditation exercises using the meditation app over 5-15 minutes once daily (QD) for up to 2 weeks. Patients also complete questionnaires before and after meditation sessions and participate in an interview over 10 minutes. GROUP II (WAITLIST CONTROL): Patients receive supportive care, such as access to social workers, support groups, spiritual care, or other patient services for up to 2 weeks. Patients also complete questionnaires over 15-20 minutes and participate in an interview over 10 minutes.

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

M D Anderson Cancer Center, Houston, Texas, United States

Contact Details

Name: Gabriel Lopez

Affiliation: M.D. Anderson Cancer Center

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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