Clinical trial · Interventional
Reduction of Pre-operative Anxiety Using a Specially Designed Educational Program for Breast Cancer Patients Undergoing Surgery: a Randomized Controlled Trial
NCT05887856CI-TRIAL-00082168PAUSDEunknownN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This study aims to find out that if a specially designed educational program can help in reduction of pre-operative anxiety in breast cancer patients undergoing surgery as a part of their treatment.
Conditions
Conditions (3)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Anxiety | — | UNRESOLVED | — |
| Patient Satisfaction | — | UNRESOLVED | — |
| Preoperative Anxiety | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| comprehensive educational program for reduction of Pre-Operative Anxiety | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- ACTIVE_COMPARATOR
- label
- Intervention Group
- description
- Volunteers in the Intervention group will receive specially designed educational program which will be aimed at reduction of pre-operative anxiety in breast cancer patients undergoing surgery as a part of their treatment.
- interventionNames
- Other: comprehensive educational program for reduction of Pre-Operative Anxiety
- type
- NO_INTERVENTION
- label
- Non-Intervention Group
- description
- Non-Intervention group will get the usual standard information as per existing protocols which includes 1. Explanation of surgical procedure by primary team. 2. Information about anesthesia on pre-operative anesthesia assessment. 3. Phone call from Primary team explaining surgery details one day prior to surgery in case of day case surgery. 4. Information about surgery on admission from floor resident in case of Pre-Op Admission. Afore mentioned practices are standard at SKMCH and RC and will remain same for both intervention and non-intervention group.
Primary outcomes (1)
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
- Maximum age
- 70 Years
Show eligibility criteria text
Inclusion Criteria: 1. 18 to 70 years of age. 2. Known cases of Breast Cancer. 3. Undergoing Breast Surgery as a part of treatment. 4. Availability of Personal smart phone at home. 5. Written informed Consent given for participation in trial. 6. Females. Exclusion Criteria: 1. Less than 18 years or more than 70 years of age. 2. Stage IV patients undergoing palliative breast surgery. 3. Patient having chronic pain. 4. Un-availability of smart phone. 5. Patients with known psychiatric/depression disorders. 6. Previous history of another treated carcinoma. 7. Patients with re-current breast carcinoma. 8. Male Patients are excluded from study.
References
Publications (0)
Data not yet available
No reference posted for this study.