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Yoga Intervention in Supporting Children With Cancer and Their Parents During Chemotherapy Infusion

A Preliminary Pilot Study to Tailor and Evaluate the Feasibility of Child and Parent Yoga (CAPY) During Chemotherapy Infusion

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04034914
Enrollment
10
Registered
2019-07-26
Start date
2019-08-07
Completion date
2020-06-30
Last updated
2020-07-24

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 trial studies how well Yoga works in supporting children with cancer and their parents during chemotherapy infusion. Pediatric cancer and its treatment is one of life's most stressful events for children and their parents. Yoga is an ancient holistic healing science that incorporates postures, breathing, relaxation, and meditation to facilitate harmony between body, mind, and spirit. Participating in Yoga exercise may improve the negative psychosocial effects in children with cancer and their parents during chemotherapy treatment.

Detailed description

PRIMARY OBJECTIVES: * To determine the feasibility of Yoga for children with cancer and their parents, specifically * Identify possible required modifications for safe and feasible practice during infusions. * Obtain recruitment estimates and determine barriers. * Assess satisfaction. SECONDARY OBJECTIVES: * To determine the feasibility of administering and acceptability of measures to assess preliminary efficacy of Yoga for the following outcomes: * Child psychological distress (stress, anxiety). * Parent psychological distress (stress, anxiety, anger, depression). * Child and parent physiological stress (heart rate, respiratory rate, and blood pressure). * Parent-child communication. * Child physical symptoms. OUTLINE: Patients and parents participate in up to 8 Yoga sessions consisting of check in, awareness, breathing practices, gentle movement, and relaxation over 30 minutes each.

Interventions

OTHERQuestionnaire administration

Ancillary studies

Sponsors

Vanderbilt-Ingram Cancer Center
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
8 Years to 17 Years
Healthy volunteers
Yes

Inclusion criteria

* Children: 8-17 years of age, within 4 weeks of: 1) any new cancer diagnosis or newly diagnosed relapsed cancer, and 2) medical clearance who anticipate 3-weeks of continous contact with Monroe Carell Jr. Children's Hospital. * Parents: 18 years of age and older, child's primary caregiver (planning to attend appointments, infusions visits, or be in hospital rooms/clinics) or secondary caregiver (an as needed back-up to primary). Children and Parents: able to speak and understand English, absence of cognitive impairment, and willing to engage in Yoga as part of a dyad.

Exclusion criteria

* CHILDREN: Medical conditions that would prohibit the safe implementation of a Yoga practice * PARENTS: Practices Yoga weekly * PARENTS: Pregnant or plans to become pregnant during next 3 months * CHILDREN AND PARENTS: Unwilling to work as a dyad.

Design outcomes

Primary

MeasureTime frameDescription
Participant satisfactionUp to 2 yearsThe total number of responses to the 14 satisfaction questions with a rating \> 4 (maximum rating = 7) will be generated for each of the 5 parent participants. It is expected that all participants will exceed that threshold for all questions. If not, frequency distributions will be used to summarize the responses to each of the 14 items to assess which produced the lower ratings. Responses to open-ended questions will be analyzed qualitatively. Findings from both components of the satisfaction survey (program satisfaction and yoga survey) will be used to revise the Yoga protocol as needed.
ModificationsUp to 2 yearsWill be assessed qualitatively. A tally of the specific modifications will be maintained to determine if particular modification are made more frequently than others.
RecruitmentUp to 2 yearsThe total number of eligible child-parent dyads approached to achieve an enrolled sample of 5 dyads will be tallied.
RetentionUp to 2 yearsThe number of the enrolled child-parent dyads who complete both the self-report assessments required at baseline (T1 - prior to first Yoga session), the Yoga protocol, and the measures at the end-of-infusion (T2 - prior to last Yoga session) will be tallied. The proportion completing will be used to inform the level of over-recruitment required in future studies of efficacy.
BarriersUp to 2 yearsParticipants who do not complete the study will be contacted and queried as to the reason for the lack of completion. A tally of the specific barriers will be maintained to determine if particular barriers are encountered more frequently than others. This information will inform possible modifications required to the protocol in future research.

Secondary

MeasureTime frameDescription
Child psychological distressUp to 2 yearsWill assess child distress using Patient-Reported Outcomes Measurement Information System (PROMIS) Pediatric Psychological Stress Experiences- Short Form
Parent psychological distressUp to 2 yearsWill assess parent distress using the PROMIS Depression - Short Form
Child and parent physiological stressUp to 2 yearsWill assess blood pressure
Parent-child communicationUp to 2 yearsWill be assessed using the Parent-Adolescent Communication Scale (PACS). Participants answer 20-40 questions. A total score is calculated ranging from 20-100 with higher scores indicating more positive communication.
Child physical symptomsUp to 2 yearsWill be assessed using the PROMIS Pediatric Physical Stress Experiences -Short Form.

Countries

United States

Outcome results

None listed

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