Memory Training Intervention for Breast Cancer Survivors

NCT ID: NCT01497015

Last Updated: 2023-02-23

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 88 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2008-09-30
• Study Completion Date: 2012-12-31

Brief Summary

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.

Detailed Description

Memory deficits are a prevalent, bothersome, and potentially debilitating symptom for millions of breast cancer survivors (BCS). Evidence-based treatment is difficult because there has been little intervention research in this area. Memory training may be a viable treatment option for BCS in need. Therefore, the purpose of this study is to examine the acceptability, usefulness, and preliminary efficacy of the memory training intervention from the Advanced Cognitive Training in Vital Elderly (ACTIVE) trial, the largest controlled trial of cognitive interventions in the behavioral sciences. The memory training intervention will be compared to attention control and no-contact control groups. Specific aims are to (1) evaluate the acceptability and usefulness of the memory intervention in BCS and (2) establish preliminary efficacy of the ACTIVE memory training intervention relative to attention control and no-contact control conditions. Acceptability and usefulness will be assessed through self-report. Memory will be assessed through objective neuropsychological tests. A total of 108 eligible BCS will be randomized to memory training, attention control, or no-contact control. A blinded and trained tester will perform data collection and neuropsychological testing at three time points: baseline prior to the intervention, immediately post-intervention, and 2 months post-intervention. Findings will provide information about the acceptability, usefulness, and preliminary efficacy of the ACTIVE memory training intervention on memory performance in BCS. Positive results will lead to a larger, full-scale study to determine efficacy of memory training interventions for BCS. Nursing interventional research in this area is vital to the development of evidence-based interventions to address memory deficits in BCS.

Conditions

Breast Cancer

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: SUPPORTIVE_CARE
• Blinding Strategy: SINGLE

Study Groups

memory training

memory training 10 1-hour sessions with interventionist to be delivered over 6-8 weeks

Group Type: EXPERIMENTAL

memory training

Intervention Type: BEHAVIORAL

10 1-hour sessions over 6-8 weeks

speed of processing training

Speed of processing training 10 1-hour sessions delivered over 6-8 weeks

Group Type: EXPERIMENTAL

speed of processing training

Intervention Type: BEHAVIORAL

10 1-hour sessions delivered over 6-8 weeks

waitlist control

Breast cancer survivors will be randomized to 1 of 3 groups: memory training, speed of process training or waitlist control

Group Type: EXPERIMENTAL

waitlist control

Intervention Type: BEHAVIORAL

Breast cancer survivors will receive the speed of processing training compact disc in the mail after study completion.

Interventions

memory training

10 1-hour sessions over 6-8 weeks

Intervention Type: BEHAVIORAL

speed of processing training

10 1-hour sessions delivered over 6-8 weeks

Intervention Type: BEHAVIORAL

waitlist control

Breast cancer survivors will receive the speed of processing training compact disc in the mail after study completion.

Intervention Type: BEHAVIORAL

Eligibility Criteria

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).

• Minimum Eligible Age: 40 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

Indiana University

OTHER

Sponsor Role: lead

Responsible Party

Diane Von Ah

Associate Professor, Department Chair, School of Nursing

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Diane Von Ah, PhD, RN, CNA

Role: PRINCIPAL_INVESTIGATOR

Indiana University

Andrew Saykin, PsyD

Role: STUDY_DIRECTOR

Indiana University

Frederick Unverzagt, PhD

Role: STUDY_DIRECTOR

Indiana University

Janet Carpenter, PhD, RN

Role: STUDY_DIRECTOR

Indiana University

Patrick Monahan, PhD

Role: STUDY_DIRECTOR

Indiana University

Locations

Indiana University

Indianapolis, Indiana, United States

Countries

United States

Other Identifiers

64194

Identifier Type: -

Identifier Source: org_study_id