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EXCEL-Punjabi: A Culturally Tailored Exercise Oncology Pilot Feasibility Intervention

EXCEL-Punjabi: Tailored Exercise Oncology for the South Asian Population

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07643389
Acronym
EXCEL-Punjabi
Enrollment
12
Registered
2026-06-11
Start date
2025-07-01
Completion date
2025-12-12
Last updated
2026-06-11

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

Conditions

Cancer

Keywords

exercise oncology, culturally tailored, South Asian, Punjabi, Exercise, Cancer, Pilot, Feasibility

Brief summary

The goal of this pilot feasibility study is to explore the feasibility and exploratory effects of a culturally-tailored exercise oncology intervention in Punjabi-speaking individuals of South Asian heritage and their support persons. The main questions it aims to answer are: 1. What is the feasibility and acceptability of the EXCEL-Punjabi intervention? 2. What are the exploratory effects (i.e., psychosocial and physical changes) before and after program delivery? Participants will take part in a 12-week exercise oncology intervention consisting of twice weekly hour long multimodal circuit-based exercise sessions. They will also complete questionnaires and functional fitness assessments pre- and post- intervention.

Interventions

BEHAVIORALEXCEL-Punjabi

Culturally Tailored Exercise Oncology Intervention

Sponsors

University of Calgary
Lead SponsorOTHER
Canadian Institutes of Health Research (CIHR)
CollaboratorOTHER_GOV

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

Pilot Feasibility Study

Eligibility

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

Inclusion criteria

* Punjabi-speaking * Self-identified as being of South Asian heritage * over the age of 18 * pre-, post-, or currently receiving cancer treatment or a support person of an individual living with and beyond cancer * cleared to participate in, at minimum, mild intensity exercise by a Clinical Exercise Physiologist * Able to provide informed consent

Exclusion criteria

* under the age of 18 * not cleared to exercise by a Clinical Exercise Physiologist

Design outcomes

Primary

MeasureTime frameDescription
Measurement CompletionBaseline to the end of the intervention (12 weeks)Participants who completed all pre- and post- questionnaires and functional assessments

Secondary

MeasureTime frameDescription
ReferralsBaseline to end of intervention (12 weeks)Number of participants referred to intervention
ConsentedRecruitment to end of intervention (12 weeks)Number of participants who consented to participate in the intervention
EnrolledBaseline (week 0)Number of participants who enrolled (i.e. completed baseline assessments)
AttendanceBaseline to end of intervention (12 weeks)Intervention Attendance
Adverse EventsBaseline to end of intervention (12 weeks)Using the standardized Common Terminology Criteria for Adverse Events Version 6.0
Time Required to Deliver and Implement InterventionFrom recruitment to end of intervention (12 weeks)Time requirement to deliver intervention
Physical Activity LevelBaseline to end of intervention (12 weeks)The Godin Leisure Time Exercise Questionnaire is used to determine subjective levels of physical activity in each participant. Participants report how many times per week they partake in mild, moderate, and/or strenuous exercise. Higher scores indicate a more physically active lifestyle.
Cancer related symptomsBaseline to end of intervention (12 weeks)Change in Edmonton Symptom Assessment Scale - revised: cancer. Scale is from 0-10, where 0 means the symptom is absent and 10 means the worst possible severity of the symptom is being experienced.
Health Related Quality of LifeBaseline to end of intervention (12 weeks)Change in EuroQual - 5Dimensions (EQ-5D) tool - first section is a questionnaire; last section uses a scale from 0-100, where 0 means the worst health imaginable and 100 means the best health imaginable.
FatigueBaseline to end of intervention (12 weeks)Change in Functional Assessment of Chronic Illness Therapy - Fatigue subscale - scale is from 0-4, where 0 means "not at all" and 4 means "very much".
Cancer Related Quality of LifeBaseline to end of intervention (12 weeks)A 5-point Likert scale (0 = not at all, to 4 = very much) to track wellbeing over the course of the cancer journey.
Exercise Barriers Self-EfficacyBaseline to end of intervention (12 weeks)Exercise barriers and facilitators questionnaire
CognitionBaseline to end of intervention (12 weeks)Cancer related cognition using the Functional Assessment of Cancer Therapy - Cognition questionnaire. A 37-item, self-report questionnaire used to evaluate how cancer patients perceive their own cognitive abilities
Aerobic CapacityBaseline to end of intervention (12 weeks)In-person participants will be assessed on change in 6-minute walk test (m) results
Lower body strengthBaseline to end of intervention (12 weeks)Change in sit-to-stand (number of repetitions in 30 seconds)
Upper extremity flexibilityBaseline to end of intervention (12 weeks)Change in active shoulder flexion range of motion (degrees)
BalanceBaseline to end of intervention (12 weeks)Change in one legged stance test (seconds)

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 12, 2026