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Impact of a Mobile Mindfulness Program on Fatigue in People with Colorectal Cancer: A Pre Post Study

Effect of Mobile Mindfulness Based Stress Reduction Program for Fatigue in Colo rectal Cancer Patients: A pre-post Experimental Study - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/05/087357
Enrollment
26
Registered
2025-05-22
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Health Condition 1: C189- Malignant neoplasm of colon, unspecified Health Condition 2: C19- Malignant neoplasm of rectosigmoidjunction Health Condition 3: C20- Malignant neoplasm of rectum Health Condition 4: C218- Malignant neoplasm of overlappingsites of rectum, anus and anal canal

Interventions

Intervention1: Mobile Mindfulness Based Stress Reduction Program for Fatigue: Participants will engage in mindfulness practices for 20 minutes per day 6 days a week totally 120 minutes per week they w

Sponsors

Nitte Deemed to be University
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Diagnosed colorectal cancer patients undergoing chemotherapy. Age above 18 years. Able to use a Smartphone and access the mobile mindfulness program. Willing to participate in a 6-week intervention with follow ups. Medically stable and cleared for participation by an oncologist

Exclusion criteria

Exclusion criteria: Patients with severe cognitive impairments or psychiatric conditions Individuals already practice formal mindfulness or meditation regularly. Patients with severe visual or hearing impairments that prevent using the mobile application. Patients who do not have consistent access to a Smartphone or internet. Any medical condition that prevents participation in a structured mindfulness program

Design outcomes

Primary

MeasureTime frame
Fatigue symptom inventory scale, Medical outcomes studies short form 36Timepoint: pre intervention post intervention after 6 weeks

Secondary

MeasureTime frame
nilTimepoint: nil

Countries

India

Contacts

Public ContactDr Purusotham Chippala

Nitte Institute of Physiotherapy (Deemed to be University)

chippala_puru@nitte.edu.in9916460185

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026