Clinical trial · Interventional
Benson Relaxation Technique Effectiveness on Pain and Quality of Life Post Reconstructive Mammoplasty
NCT07032883CI-TRIAL-00091306not yet recruitingN/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)
The purpose of this study is to evaluate effectiveness of benson relaxation technique on pain and quality of life post mammoplasty.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (3)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Benson relaxation technique | Other | — | UNRESOLVED |
| Medications | Drug | — | UNRESOLVED |
| Routine physiotherapy program | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Benson relaxation technique and routine physiotherapy program group
- description
- This group will receive Benson relaxation technique for duration up to 20 min twice daily in addition to medical therapy and a routine physical therapy program for 40 minutes, twice daily for 4 weeks.
- interventionNames
- Other: Benson relaxation technique
- Other: Routine physiotherapy program
- Drug: Medications
- type
- ACTIVE_COMPARATOR
- label
- routine physiotherapy program group
- description
- This group will receive medical therapy and a routine physical therapy program for 40 minutes, twice daily for 4 weeks.
- interventionNames
- Other: Routine physiotherapy program
- Drug: Medications
Primary outcomes (2)
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 25 Years
- Maximum age
- 50 Years
Show eligibility criteria text
Inclusion Criteria: * Only female patients underwent reconstruction mammoplasty will participate in the study. * Female patients who stopped chemotherapy at least one month before participation in the study. * Female patients with chronic pain following cosmetic breast surgery. * All patients who will accept to participate in the study after one week from operation. Exclusion Criteria: * Patients have irritable bowel syndrome. * Patients have urinary incontinence. * Chronic diseases like multiple sclerosis, polyneuropathy , diabetes and fibromyalgia. * Patients have cognitive disorder. * Patients with chronic and severe back pain. * Sepsis with complications postoperative hemodynamics. * Patients take anti-psychotic drugs. * Patients take hypnotic drugs.
References
Publications (0)
Data not yet available
No reference posted for this study.