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Status unknownNCT05881070MANNERUpdated May 30, 2023

Effectiveness of Mobile-health Self Management on Quality of Life of Patients Undergoing Chemotherapy

An interventional study of Mobile-health self management in Cancer, Chemotherapy Effect and Quality of Life, sponsored by Universitas Muhammadiyah Yogyakarta. Status unknown. Open to participants aged 20 Years and older. Per ClinicalTrials.gov, last updated 2023-05-30.

Sponsored by Universitas Muhammadiyah Yogyakarta · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified May 2023), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Not applicable
Ages
20 Years and older
Sex
All
01

Study summary

The study will design and evaluate the use of mobile-health based self-management on self-efficacy and quality of life of patients undergoing chemotherapy.

Read the detailed description

The study will design and evaluate the use of mobile-health based self-management on self-efficacy and quality of life of patients undergoing chemotherapy.

02

Conditions studied

  • Cancer
  • Chemotherapy Effect
  • Quality of Life
  • Self Efficacy

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03

In context

Neoplasms

9,617 studies on the registry are indexed under Neoplasms; 2,508 are open to participants now.

This study's planned enrollment of 50 is close to the median of 50 across 7,432 interventional studies indexed under Neoplasms.

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Lead sponsor

Universitas Muhammadiyah Yogyakarta is the lead sponsor of 7 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • adult patients diagnosed with cancer
  • patients who use smart phone

Exclusion criteria

Exclusion Criteria:

  • patients with cancer with comorbidity
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
50 participants (estimated)

Study arms

  • Experimental
    Mobile health self-management

    Behavioral: Mobile-health self management

Interventions

  • BehavioralMobile-health self management

    Mobile-health self management

06

What researchers measure

Primary outcomes

  1. Patient's Quality of life

    The patient's quality of life will be assessed before (T0) and after intervention (T1). The measurement will use EORTC. The score will range from 0-100, where higher score reflects a better quality of life.

    Time frame: Four weeks

  2. Patient's Self-efficacy

    The patients self-efficacy will be measured pre and post intervention. The measurement will use the Self-Efficacy for Managing Chronic Disease Scale. The scale has been widely used in cancer setting. Respondents will rate their confidence to perform six self-management behaviours (1 = 'not at all confident' to 10 = 'totally confident'). A mean score is calculated (range 1 to 10). A high score indicates high self-efficacy.

    Time frame: four weeks

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 30, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05881070
Lead sponsor
Universitas Muhammadiyah Yogyakarta
Responsible party
Erna Rochmawati (Associate Professor, Universitas Muhammadiyah Yogyakarta) — Principal investigator
First posted
May 30, 2023
Start date
Jun 15, 2023 (estimated)
Primary completion
Aug 31, 2023 (estimated)
Completion
Sep 30, 2023 (estimated)
Last update
May 30, 2023

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in May 2023. You cannot join it, but the record below documents what was studied.

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