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Not yet recruitingNCT07883109Updated Oct 20, 2026

Podcast-Based Psychosocial Support for Women Newly Diagnosed With Breast Cancer

An interventional study of Psychosocial Support Program in Breast Cancer, sponsored by Mei Man. Not yet recruiting. Open to female participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-10-20.

Sponsored by Mei Man · Not applicable, Interventional, and Supportive care

Updated Oct 20, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
80
Allocation
Non-randomized
Ages
18 Years and older
Sex
Female
01

Study summary

This study will evaluate a podcast-based psychosocial support program for women who have been newly diagnosed with breast cancer. The program is designed to provide accessible information and psychological support during the period between diagnosis and the start of cancer treatment.

Participants will be assigned to either an experimental group or a control group. Participants in the experimental group will receive a series of podcast episodes addressing common concerns related to breast cancer diagnosis and treatment, psychological adjustment, and coping. Participants in the control group will receive usual care.

Participants will complete questionnaires before the program and approximately 1 month after the intervention. The study will assess changes in anxiety, uncertainty, demoralization, and other psychological outcomes. The findings will help determine whether podcast-based psychosocial support may provide useful support for women adjusting to a new breast cancer diagnosis.

02

Conditions studied

  • Breast Cancer

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Keywords

  • Breast Cancer Patients
03

In context

Breast Neoplasms

12,815 studies on the registry are indexed under Breast Neoplasms; 2,920 are open to participants now.

This study's planned enrollment of 80 is above the median of 72 across 9,494 interventional studies indexed under Breast Neoplasms.

Browse Breast Neoplasms studies →

Lead sponsor

This is the only study on the registry with Mei Man as lead sponsor.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
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

Women aged 20 years or older.

Newly diagnosed with breast cancer based on histopathological or cytological confirmation.

Have not yet received breast cancer-related treatment or breast cancer surgery.

Exclusion criteria

Exclusion Criteria:

-

05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
80 participants (estimated)

Study arms

  • Experimental
    Experimental Group

    Participants will receive the podcast-based psychosocial support program in addition to usual care. The program is designed to support psychological adjustment, reduce

    Other: Psychosocial Support Program

  • No intervention
    Control Group

    Participants will receive usual care without the podcast-based psychosocial support program.

Interventions

  • OtherPsychosocial Support Program

    Participants in the experimental group will access the podcast content during the intervention period in addition to usual care.

    Also known as: Behavioral

06

What researchers measure

Primary outcomes

  1. Anxiety Symptoms Measured by the Hospital Anxiety and Depression Scale-Anxiety Subscale (HADS-A)

    Anxiety symptoms will be assessed using the anxiety subscale of the Hospital Anxiety and Depression Scale (HADS-A), which consists of 7 items. Each item is scored from 0 to 3, yielding a total score ranging from 0 to 21 points. Higher scores indicate greater anxiety symptoms. The outcome measure is the HADS-A total score, expressed in points.

    Time frame: Baseline and approximately 1 month after the intervention

  2. Depressive Symptoms Measured by the Hospital Anxiety and Depression Scale-Depression Subscale (HADS-D)

    Depressive symptoms will be assessed using the depression subscale of the Hospital Anxiety and Depression Scale (HADS-D), which consists of 7 items. Each item is scored from 0 to 3, yielding a total score ranging from 0 to 21 points. Higher scores indicate greater depressive symptoms. The outcome measure is the HADS-D total score, expressed in points.

    Time frame: At baseline before the intervention and 1 month after the intervention.

07

Study locations

No study locations are listed for this record.

08

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Oct 2026; primary completion for Aug 2027, 9 months later.

Of 2,272 non-industry interventional studies with no phase under Breast Neoplasms, half reached primary completion within 34 months of starting (the median), counting those still running; a quarter within 16 and three quarters within 69. This study's planned 9 months is below that.

Counting every sponsor, half of 2,345 studies reached it within 34 months; a quarter within 16 and three quarters within 69.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 6, 2026
First posted
Oct 20, 2026
StartEst.
Oct 15, 2026
Primary completionEst.
Aug 1, 2027
CompletionEst.
Aug 1, 2027
Last update
Oct 20, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Oct 20, 2026
Show all 1 update
  1. Oct 20, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

09

Registry details

Key details

Study ID
NCT07883109
Lead sponsor
Mei Man
Collaborators
Tri-Service General Hospital (TSGH)
Responsible party
Mei Man (Principal Investigator, National Defense Medical Center, Taiwan) — Sponsor-investigator
First posted
Oct 20, 2026
Start date
Oct 15, 2026 (estimated)
Primary completion
Aug 1, 2027 (estimated)
Completion
Aug 1, 2027 (estimated)
Last update
Oct 20, 2026

Oversight

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

Not currently enrolling

This study is not yet recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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