Clinical trial · Interventional
Health Benefits of HIT for Breast Cancer Patients
The Efficacy of Reduced-exertion High-intensity Interval Training for Improving Health and Well-being in Newly Diagnosed Female Breast Cancer Patients
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): Logistical problems meant that the study was no longer feasible.
Summary
Brief summary (as posted)
Treatment of cancer patients should not only involve removing the cancer, but should also focus on maintaining good health and well-being and quality of life. This can be done by offering patients suitable rehabilitation programmes. Previous research has shown that such programmes need to involve exercise alongside other components, such as psychological support. To date most studies have looked at the positive effects of moderate-intensity exercise such as brisk walking, but this type of exercise is time-consuming and often not done by many patients. Shorter-duration exercise routines consisting of repeated short sprints have been found to improve general health just as well, but one of the most time-efficient routines (termed 'reduced-exertion high-intensity interval training', or 'REHIT') has not been studied in cancer patients. REHIT involves 3 exercise sessions per week, each only 10 minutes long. This makes it an ideal routine to combine with other components of a cancer rehabilitation programme. The present study will determine whether REHIT can improve important markers of health and well-being in newly diagnosed breast cancer patients. To achieve this the investigators will recruit up to 30 patients and divide them into a group who will do REHIT before and for up to 6 weeks after their cancer surgery, and a control group who will receive standard care. Markers of health and well-being will be measured at the start of the study, \~1 week after surgery, and \~7 weeks after surgery. Any changes will be compared between the exercise group and the control group. If beneficial effects are found with the REHIT intervention then this could be more widely implemented as part of cancer treatment. This study is funded by Nuffield Health and will be performed in Oxford, UK.
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 (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Cognitive behavioral therapy (CBT) | Behavioral | — | UNRESOLVED |
| Reduced-exertion, high-intensity interval training (REHIT) | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Exercise
- description
- Patients in the Exercise group will follow a fully-supervised exercise routine (Reduced-exertion, high-intensity interval training (REHIT)) with 3 weekly 10-minute training sessions consisting of easy cycling interspersed with 2 brief 'all-out' cycle sprints. Patients in this group will also be offered up to 6 sessions of cognitive behavioral therapy. The duration of the intervention will be the weeks between enrolling in the study and surgery (\~1-4 weeks), as well as an additional period of up to 6 weeks following surgery.
- interventionNames
- Behavioral: Reduced-exertion, high-intensity interval training (REHIT)
- Behavioral: Cognitive behavioral therapy (CBT)
- type
- NO_INTERVENTION
- label
- Standard care
- description
- Patients allocated to the Standard Care group will receive the care they would have also received if they would not have participated in the study. They will however undergo the same testing sessions as patients in the Exercise group.
Primary outcomes (1)
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 35 Years
- Maximum age
- 60 Years
Show eligibility criteria text
Inclusion Criteria: 1. Recent diagnosis of biopsy-proven primary invasive breast cancer 2. Pre- or post-menopausal women 3. World Health Organisation Performance status 0-2 4. No distant metastasis 5. On a treatment plan of: 1. surgery (breast conservation surgery or mastectomy with or without reconstruction, including axillary surgery) 2. Adjuvant treatment with hormonal therapy and/or radiotherapy 3. Adjuvant chemotherapy with or without anti-Her-2 therapy 6. Can start the study within 1 week of diagnosis and prior to surgery 7. Have surgery arranged within 1-4 weeks of diagnosis 8. All receptor statuses are eligible Exclusion Criteria: 1. BMI \> 35 kg·m-2 2. Age \< 35 y or \> 60 y 3. Men 4. Verbal self-report of undertaking five or more structured exercise sessions per week, perceived as being moderate-to-vigorous intensity, and each session being ≥ 30 minutes in duration 5. Contraindications to exercise as determined using the Physical Activity Readiness Questionnaire (PAR-Q) 6. Any known significant cardiovascular (except controlled hypertension), pulmonary (except treated/controlled asthma) or metabolic disease (except hypercholesterolemia or type II diabetes) 7. Auto-immune disease or exercise-limiting inflammatory arthritis 8. Distant metastasis 9. Secondary breast cancer or previous diagnosis of invasive cancer and treatment within last 5 years except 1. Localised basal cell carcinoma or squamous cell carcinoma of skin 2. In situ melanoma 3. Cervical intraepithelial neoplasia (CIN) 10. Neoadjuvant chemotherapy
References
Publications (0)
Data not yet available