MedPath

Yoga for Adolescent and Young Adult Non-Curative Cancer Patients

Not Applicable
Completed
Conditions
Advanced Cancer
Interventions
Behavioral: Hatha Yoga
Registration Number
NCT01901237
Lead Sponsor
Rob Rutledge
Brief Summary

Adolescents and young adults who are living with cancer are not benefiting from the same age-appropriate physical and psychosocial care, as are children and older adults. As a result, their unique needs often go unmet or unaddressed. Studies have demonstrated that a lack of age-appropriate care may be responsible for a deceased quality of life. Studies have also shown that physical activity is able to reduce many of the negative side-effects linked to cancer and its treatment (e.g., nausea, vomiting, fatigue). A light form of physical activity that is both safe and manageable for cancer patients is yoga. The purpose of this study is to examine the achievability and safety of a light 7-week home/hospice-based Hatha yoga program (available on DVD) in the adolescent and young adult non-curative cancer population. This study will also examine the ability of yoga to reduce cancer related side effects.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
5
Inclusion Criteria
  • Diagnosed with a non-curative cancer and assigned to non-curative or palliative care
  • Between 15-39 years of age
  • Have primary physician/oncologist consent to participate
Exclusion Criteria
  • Experience any medical conditions that contraindicate yoga (e.g., bone metastases)
  • Exhibit cognitive limitations (e.g., psychiatric disorders)
  • Score below 30% on Palliative Performance Status Scale

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Hatha Yoga ProgramHatha YogaSingle-arm pilot study of a 7-week home/hospice-based Hatha yoga program for adolescent and young adults with non-curative cancer.
Primary Outcome Measures
NameTimeMethod
Feasibility: RecruitmentFinal: end of week 7

Recruitment will be calculated by the number of patients who consent to participate, divided by the number of eligible participants recommended by the primary oncologist/physician.

Feasibility: RetentionFinal: end of week 7

Retention: Will be determined by reporting the number of participants who complete the baseline and post-program questionnaire and follow-up testing.

Feasibility: AdherenceFinal: end of week 7

Adherence: Participants will be asked to record the number of yoga sessions performed each week. Overall adherence will be calculated by summing the actual number of sessions the participant engaged in, divided by the recommended number of sessions.

SafetyFinal: end of week 7

Safety: Any adverse events reported by the participant will be recorded.

Secondary Outcome Measures
NameTimeMethod
Changes in Quality of LifeBaseline: week 1; Final: week 7

Participants will be asked to complete the Functional Assessment of Chronic Illness Therapy - Palliative Care subscale (FACIT-Pal) and the Functional Assessment of Chronic Illness Therapy - Spiritual Well-Being subscale (FACIT-Sp) at baseline and post-intervention.

Trial Locations

Locations (1)

Dalhousie University

🇨🇦

Halifax, Nova Scotia, Canada

© Copyright 2025. All Rights Reserved by MedPath