Clinical trial · Interventional
Memory Training Intervention for Breast Cancer Survivors
- 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 is a randomized controlled trial to evaluate the ACTIVE memory training intervention and ACTIVE speed of processing training to waitlist, no-contact control conditions. Specific aims and hypotheses are: Aim 1: Evaluate the acceptability and usefulness of the ACTIVE memory intervention among Breast Cancer Survivors (BCS). Hypothesis 1: BCS assigned to the memory intervention arm will perceive the intervention as more acceptable and useful than BCS assigned to the attention control condition. Aim 2: Establish preliminary efficacy of the ACTIVE memory training intervention relative to the attention control and no-contact control conditions. Hypothesis 2: Memory training will result in greater memory enhancement immediately post and 2-months post-intervention relative to attention control or no-contact control conditions.
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 |
|---|---|---|---|
| memory training | Behavioral | — | UNRESOLVED |
| speed of processing training | Behavioral | — | UNRESOLVED |
| waitlist control | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (3)
- type
- EXPERIMENTAL
- label
- memory training
- description
- memory training 10 1-hour sessions with interventionist to be delivered over 6-8 weeks
- interventionNames
- Behavioral: memory training
- type
- EXPERIMENTAL
- label
- speed of processing training
- description
- Speed of processing training 10 1-hour sessions delivered over 6-8 weeks
- interventionNames
- Behavioral: speed of processing training
- type
- EXPERIMENTAL
- label
- waitlist control
- description
- Breast cancer survivors will be randomized to 1 of 3 groups: memory training, speed of process training or waitlist control
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 40 Years
Show eligibility criteria text
Inclusion Criteria: 1. female gender (breast cancer is rare in men); 2. self-reported memory impairment and desire for treatment (to focus on BCS in greatest need); 3. first diagnosis of non-metastatic breast cancer (to control for multiple treatments or brain metastases in women with recurrent or metastatic disease); 4. ≥ 1 year post-treatment including surgery, radiation, and/or chemotherapy (reduce confounding factors related to acute effects of treatment);32 5. age ≥ 40 years (our prior studies indicate approximately 75% of BCS meet this criterion and reduce sample variability); 6. post-menopausal (majority are post-menopausal at diagnosis and reduce sample variability); and 7. able to read, write, understand, and speak English (to ensure informed consent). Exclusion Criteria: Women will be excluded if they have other co-morbidities or deficits that would sufficiently impair performance or inhibit cognitive training including: 1. substantial cognitive decline (score \< 24 on the Mini Mental State Exam (MMSE);33 2. history of stroke, encephalitis, traumatic brain injury, brain surgery, dementia, Alzheimer disease, or Parkinson disease; 3. cranial radiation therapy or intrathecal therapy; 4. current active major depression or substance abuse or history of bipolar disorder, psychosis, schizophrenia, or learning disability; 5. history of or current other cancer except for basal cell skin cancer; or 6. receiving other cognitive training (to avoid exposure to other training).
References
Publications (0)
Data not yet available