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Oncology - Bolstering Oral Agent Reporting Related to Distress (ON-BOARD)

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McGill University

Status

Completed

Conditions

Oral Chemotherapy

Treatments

Other: Oral chemotherapy information and support

Study type

Interventional

Funder types

Other

Identifiers

NCT04984850
2021-2861

Details and patient eligibility

About

Individuals on oral chemotherapy (OC) often face many challenges requiring adequate informational support, monitoring, and management. This pilot randomized control trial (RCT) aims to assess the feasibility, acceptability, and preliminary effects of a comprehensive OC intervention on medication adherence self-efficacy, medication adherence, and symptom distress.

Enrollment

52 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18 years of age or older
  • Diagnosis of cancer, any stage
  • Being followed by a care team at the affiliated hospital centre
  • About to start or within the first cycle of oral anticancer treatment (traditional cytotoxic, targeted therapy, hormonal therapy as active ongoing treatment for cancer with the aim of killing cancer cells/shrinking tumor size)
  • Has a computer/tablet/smartphone device with internet
  • The ability to communicate, read, and write in English or French

Exclusion criteria

  • Receiving IV chemotherapy, immunotherapy, and/or oral hormonal therapy as long-term maintenance treatment for prevention of cancer's return/growth of cancer cells after initial treatment
  • Significant physical or cognitive limitations that would prevent ability to participate in study as reported by patient, primary healthcare provider, or research staff
  • At imminent "end-of-life"
  • Participating in an ongoing clinical trial

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

52 participants in 2 patient groups

Intervention plus usual care
Experimental group
Treatment:
Other: Oral chemotherapy information and support
Usual care only
No Intervention group

Trial contacts and locations

1

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Central trial contact

Saima Ahmed; Jacqueline Vachon

Data sourced from clinicaltrials.gov

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