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Improving Cancer Pain Management Through Teach-Back Educational Approach for Patients and Primary Caregivers: A Pilot Study

Improving Cancer Pain Management Through Teach-Back Educational Approach for Patients and Primary Caregivers: A Pilot Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05856292
Enrollment
40
Registered
2023-05-12
Start date
2022-03-01
Completion date
2022-06-30
Last updated
2023-05-12

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

Conditions

Cancer Pain

Keywords

Cancer Pain, Education

Brief summary

This randomized prospective quantitative pilot study compared teach-back method to standardized educational method in patient and caregiver to improve cancer pain management

Detailed description

Even though there are comprehensive guidelines for cancer pain management, pain control among cancer patients and survivors is often suboptimal due to undertreatment. According to recent studies, the addition of educational interventions could improve pain relief in cancer patients. Both patients and family caregivers play an important role in delivering cancer pain self-management, especially at home. Providing knowledge for cancer pain management with optimal intervention could improve patient and caregiver outcomes. The Teach-back method, where patients and family caregivers are asked to repeat the instruction they've received from their health care professionals, can assess patients' understanding, repeat or modify the educational material if comprehension is not demonstrated. This pilot study compared the addition of the Teach-back method for cancer patients and their caregivers and its relation to cancer pain management.

Interventions

Standard cancer pain educational intervention enhanced with teach-back method

OTHERPlacebo

Standard cancer pain educational intervention without enhancement

Sponsors

Tarumanagara University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

Group 1: Placebo Group 2: Teach-Back

Eligibility

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

Inclusion criteria

* Moderate to severe pain (pain scale 4 and above) * ≥18 years old * Signed the informed consent * Willing to cooperate until the end of studies * The patient is fully conscious and able to communicate well * Cared by a family caregiver * Family caregiver able to fully function as a caregiver

Exclusion criteria

* Near-death (dying) stage * Not willing to cooperate until the end of studies * Altered mental status and communication difficulties

Design outcomes

Primary

MeasureTime frameDescription
Cancer pain managementone monthQuality of cancer pain management. Patient Global Impression Change (PGIC) scale is used to measure the overall quality of life and satisfaction as a conclusion toward the intervention

Secondary

MeasureTime frameDescription
Health Literacyone monthusing Health Literacy Short Form Survey Questionnaire (HLS-EU-SQ10-IDN) to measure the change in health literacy
Pain Levelweekly up to one monthusing Brief Pain Inventory (BPI) to measure the change in pain level
Distressweekly up to one monthusing distress thermometer to measure change in distress
Beliefone monthusing Barriers Questionnaire (BQ-13) to measure change in belief

Countries

Indonesia

Outcome results

None listed

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