| Protocol ID | NCT05946070 |
| Registration Date | 2023-07-14 |
| Status | completed |
| Sponsor | Istanbul University - Cerrahpasa |
| Country | Turkey (Türkiye) |
| Industry | not industry |
| Blinding | unblinded |
| Center Type | singel-center RCT |
| Scope | national RCT |
| First Patient In | 2023-06-23 |
| Last Patient Out | 2024-12-05 |
| Publication | n |
| Gender % | ALL |
| Mean Age | 18 Years - |
NCT05946070
Effectiveness of Mobile Based Monitoring System in the Management of Chemotherapy-Related Symptoms
| Field |
CLAUDE
claude-sonnet-4-20250514 Thinking: claude-opus-4-20250514 5232ms / 10599 tok |
OPENAI
gpt-4o Thinking: o3 4436ms / 9179 tok |
GLM
glm-5.1 5958ms / 9340 tok |
Review |
|---|---|---|---|---|
| rct_type |
parallel RCT
parallel RCT → parallel RCT
shaky reasoning✓ Unanimous
Initial: parallel RCT
Requery: parallel RCT — This is a randomized controlled trial where participants are randomly assigned to either the intervention group (using the full mobile application) or control group (receiving standard care with demo version), with each participant receiving only one treatment assignment throughout the study.
|
parallel RCT
N/A → parallel RCT
shaky reasoning✓ Unanimous
Initial: N/A
Requery: parallel RCT — The study mentions 'randomized-controlled, experimental' and involves two groups: an intervention and a control group, with no mention of crossover or cluster design.
|
parallel RCT | OK |
| cancer_status | Cancer | Cancer | Cancer | OK |
| non_cancer_spec | N/A | N/A | N/A | OK |
| setting_patient | outpatient | outpatient | outpatient | OK |
| setting_place | other | other | other | OK |
| feasibility | fully powered RCT | fully powered RCT | fully powered RCT | OK |
| intervention_pharmacologic | no | no | no | OK |
| intervention_chemo_immuno_radio |
no
no → no
shaky reasoning✓ Unanimous
Initial: no
Requery: no — The intervention being tested is a mobile application for monitoring chemotherapy-related symptoms, not chemotherapy, immunotherapy, or radiation therapy itself.
|
no
yes → no
shaky reasoning✓ Unanimous
Initial: yes
Requery: no — The trial tests a mobile monitoring system to manage chemotherapy-related symptoms, not the effectiveness of chemotherapy itself.
|
no | OK |
| intervention_complementary | no | no | no | OK |
| intervention_device | no | no | no | OK |
| intervention_psychological | no | no | no | OK |
| intervention_complex | no | no | no | OK |
| intervention_acp | no | no | no | OK |
| intervention_music | no | no | no | OK |
| intervention_screening | no | no | no | OK |
| intervention_palliative |
no
yes → no
shaky reasoning✓ Unanimous
Initial: yes
Requery: no — The intervention is a mobile application for symptom monitoring and management in chemotherapy patients, not palliative care consultation or service delivery itself.
|
no
no → no
shaky reasoning✓ Unanimous
Initial: no
Requery: no — The trial tests a mobile monitoring system for managing chemotherapy symptoms, not palliative care services or team involvement.
|
yes | – |
| intervention_education |
yes
yes → yes → no
shaky reasoning✗ No consensus
Initial: yes
Requery: yes — The mobile application provides patients with information about risk factors, symptom findings, and intervention suggestions for symptom management, making education a primary component of the intervention.
Thinking: no — This is primarily a symptom monitoring and management mobile application system, not an educational program - the educational components are secondary features supporting the main symptom tracking intervention.
|
no
no → no → yes
shaky reasoning✗ No consensus
Initial: no
Requery: no — The primary intervention involves using a mobile application for symptom monitoring and management, not primarily for education or training purposes.
Thinking: yes — The mobile app’s primary purpose is to give patients self-management guidance and recommendations for chemotherapy-related symptoms, making patient education the core component of the intervention.
|
no |
|
| intervention_digital | yes | yes | yes | OK |
| intervention_other | no | no | no | OK |
| outcome_symptom | yes | yes | yes | OK |
| outcome_qol | yes | yes | yes | OK |
| outcome_dignity | no | no | no | OK |
| outcome_cost | yes | yes | yes | OK |
| outcome_other | yes | yes | yes | OK |
| pharmacologic_sub | N/A | N/A | N/A | OK |