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Brief Mindful Meditation Practice in Improving Quality of Life in Patients With Cancer Undergoing Radiation Therapy

Use of a Brief Mindful Meditation Practice in Adult Cancer Patients Receiving Radiation Therapy

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02170350
Enrollment
17
Registered
2014-06-23
Start date
2014-06-06
Completion date
2016-08-18
Last updated
2025-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Malignant Neoplasm

Brief summary

This pilot clinical trial studies how well brief mindful mediation practice works in improving quality of life in patients with cancer undergoing radiation therapy. Brief mindful mediation practice may improve the well-being and quality of life of patients with cancer who are undergoing radiation therapy by increasing levels of mindfulness and reducing stress, anxiety/depression, and fatigue.

Detailed description

PRIMARY OBJECTIVES: I. To investigate the feasibility of a clinical trial using a brief mindful meditation practice during radiation therapy. SECONDARY OBJECTIVES: I. To explore the measurable changes in quality of life, fatigue, and mindfulness while using a brief mindful meditation practice during radiation therapy. OUTLINE: Patients use brief mindful meditation practice (sitting meditation in which the mind is guided to focus in the present, thinking of your existence, and allowing sensations to arise with an openness and curiosity) over 12 minutes daily for 14 days during radiation therapy. After completion of study, patients are followed up 4-12 weeks after completion of radiation therapy.

Interventions

OTHERQuestionnaire administration

Ancillary studies

Use brief mindful meditation practice

OTHERQuality-of-life assessment

Ancillary studies

Sponsors

Sidney Kimmel Cancer Center at Thomas Jefferson University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Pathologically proven diagnosis of cancer any stage, based upon the following minimum diagnostic workup: History & physical examination, including documentation of Karnofsky Performance Status of 70 - 100% for at least 60 days prior to study entry 2. Patients who are receiving a course of radiation therapy for curative or adjuvant intent 3. Patient who have reported fatigue moderate or higher fatigue (based on the 0-10 Fatigue scale, a fatigue score of 5 or; see Appendix III) while on radiation treatment 4. The patient must be an adult male or female 18 or older 5. Patient must be capable to read and speak English and provide study specific informed consent prior to study entry 6. No prior history of radiation therapy 7. No history of or current active drug/alcohol dependence 8. No patients being decisionally impaired 9. Patients who have home access to a computer, or compact disc audio player

Exclusion criteria

1. Patient is under the age of 18 2. Diagnosis of a non-malignant disease and receiving radiation for a pathological diagnosis that is non-cancer 3. Patient who have reported less than moderate fatigue (based on the 0-10 Fatigue scale, a fatigue score less than 5; see Appendix III) 4. Karnofsky performance status of less than 70% within the last 60 days prior to study 5. Prior history of radiation therapy 6. History of or active drug/alcohol dependence or abuse 7. Decisionally impaired patients 8. No access to a computer, or compact disc audio player 9. Patient who are unable to read and speak English

Design outcomes

Primary

MeasureTime frameDescription
Feasibility measured by the proportion of patients who are adherent, defined as successful completion of the course of home base brief mindful meditation practice (at least 8 out of 14 days) and completion of questionnaires at all time pointsUp to 12 weeks after completion of radiation therapyThe portion of patients who complete the brief mindful meditation practice intervention and questionnaires will be computed, along with a one-sided 95% exact confidence interval.

Secondary

MeasureTime frameDescription
Changes in quality of life assessed by Functional Assessment of Chronic Illness Therapy-Fatigue (FACIT-F)Baseline to up to 12 weeks after completion of radiation therapyWill be analyzed using mixed-effects linear regression. Average changes and associated 95% confidence intervals will be estimated from these models.
Changes in fatigue assessed by FACIT-FBaseline to up to 12 weeks after completion of radiation therapyWill be analyzed using mixed-effects linear regression. Average changes and associated 95% confidence intervals will be estimated from these models.
Changes in mindfulness assessed by Freiburg Mindfulness InventoryBaseline to up to 12 weeks after completion of radiation therapyWill be analyzed using mixed-effects linear regression. Average changes and associated 95% confidence intervals will be estimated from these models.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026