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Prevention of Osteoporosis in Breast Cancer Survivors

Primary Purpose

Postmenopausal Osteoporosis

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Strength/weight Training & Drug/Supplement
Drug/Supplement only
Sponsored by
University of Nebraska
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Postmenopausal Osteoporosis

Eligibility Criteria

35 Years - 75 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • read, speak and understand English;
  • be female;
  • be between the ages of 35 and 75;
  • have completed treatment (except tamoxifen) for stage 0, I or II breast cancer (i.e. surgery, chemotherapy, radiation) at least 6 months prior to admission to the study;
  • be 1 year postmenopausal (12-months amenorrheic; subjects 55-years or younger with history of hysterectomy without oophorectomy must have it confirmed by two baseline measures of FSH >40 IU/ml);
  • have a BMD T-score of -1.0 SD or lower at one or more sites (spine, hip or forearm); and
  • have agreement of their primary care provider for participation in the study.

Exclusion Criteria:

  • have a recurrence of their breast cancer;
  • currently take hormone replacement therapy, bisphosphonates, calcitonin, raloxifene, calcitriol, or glucocorticosteroids.;
  • currently do strength/weight training exercises or high impact exercises (such as running, jumping rope, high impact aerobic dance, martial arts, volleyball, or basketball) two to three times weekly;
  • have a body mass index (BMI) equal to or greater than 35;
  • have serum calcium, creatinine or TSH (if on thyroid therapy) outside the normal limits;
  • have active gastrointestinal problems such as dysphagia, esophageal disease, gastritis, duodenitis, or ulcers;
  • have Paget=s disease;
  • have renal disease (renal stones or serum creatinine levels greater than the upper normal limits);
  • have a recent history of a spinal fracture (within the past 6 months);
  • have features of an acute fracture on baseline spinal x-rays;
  • have other concomitant conditions that prohibit strength/weight training exercises, calcium, or vitamin D intake.

Sites / Locations

  • University of Nebraska Medical Center, College of Nursing
  • University of Nebraska Medical Center, College of Nursing
  • University of Nebraska Medical Center, College of Nursing
  • University of Nebraska Medical Center, College of Nursing

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

1 Strength/weight Training & Drug/Supplement

2 Drug/Supplement only

Arm Description

Subjects in the G1 group receive 1200 mg of calcium and 400 IU of vitamin D supplements per day, 35 mg of risedronate per week and strength/weight training exercises for upper and lower extremities and the spine.

Subjects in the G2 group receive the calcium, vitamin D, and risedronate, but do not participate in strength/weight training exercises.

Outcomes

Primary Outcome Measures

Bone Mineral Density
Bone Mineral Density (gm/cm2) will be measured by Dual-Energy X-ray Absorptiometry (DEXA) of the hip, spine and forearm

Secondary Outcome Measures

Muscle Strength
Muscle Strength (peak torque/body weight at 60 degrees) will be assessed using BiodexTM Velocity Spectrum Evaluation (Medical Systems, Inc., 1993)

Full Information

First Posted
December 3, 2007
Last Updated
August 31, 2023
Sponsor
University of Nebraska
Collaborators
National Institute of Nursing Research (NINR)
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1. Study Identification

Unique Protocol Identification Number
NCT00567606
Brief Title
Prevention of Osteoporosis in Breast Cancer Survivors
Official Title
Prevention of Osteoporosis in Breast Cancer Survivors
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Completed
Study Start Date
April 1, 2002 (Actual)
Primary Completion Date
undefined (undefined)
Study Completion Date
December 1, 2007 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Nebraska
Collaborators
National Institute of Nursing Research (NINR)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to test whether strength/weight training exercises enhance the effectiveness of calcium, vitamin D, and risedronate for the prevention and treatment of osteoporosis in postmenopausal breast cancer survivors.
Detailed Description
Each year, more than 192,200 women are diagnosed with breast cancer (Greenlee, Hill-Harmon, Murray, & Thun, 2001). With an increase in early detection and improved therapies, more of these women have become survivors (Vassilopoulou-Sellin & Theriault, 1994). However, many of these women are at increased risk for osteoporosis and the debilitating consequences. This increased risk occurs for two reasons. Over 50-70% of women under the age of 50 (premenopausal) who are treated with adjuvant chemotherapy experience ovarian failure and early menopause (Ali & Twibel, 1994; Cobleigh et al., 1994; Samaan et al., 1978), resulting in a long postmenopausal period of estrogen deprivation. Breast cancer survivors also are at greater risk for osteoporosis because they usually are not candidates for hormone replacement therapy (HRT). Estrogen can influence the growth of cancer in women, especially those with estrogen receptor positive tumors (ER+), and at least 60% of women have ER+ breast cancer (DeVita, Hellman & Rosenberg, 1997). While the use of HRT significantly reduces osteoporosis and the risk of forearm, vertebral, pelvic, and hip fractures in postmenopausal women (Cobleigh et al., 1994; Finkelstein, 1996), women with a history of breast cancer generally are not considered candidates for HRT. Without estrogen, women may lose up to 30% of their bone mass within the first 5-years postmenopause, with continued bone loss over time, but at a slower rate. Very little information has been reported on the incidence and treatment of osteoporosis in breast cancer survivors (Headley et al., 1998; Hosking et al., 1998). Osteoporosis is a major risk factor for chronic disability and especially hip fractures. The majority of individuals with hip fractures never return to prefracture functional status and estimates of health care costs for individuals with osteoporosis exceed the costs for those with congestive heart failure or with asthma (U.S. Congress Office of Technology Assessment, 1994; Ray, Chan, Thamer & Meltin, 1997). Prevention and treatment of osteoporosis, by increasing bone mineral density (BMD) and muscle strength, may decrease the chronic disabilities associated with osteoporosis and improve quality and quantity of life (Mahon, 1998). Research on effective alternatives to HRT for the prevention of osteoporosis in breast cancer survivors has been targeted as a priority area by the Office of Cancer Survivorship (Division of Cancer Control and Population Sciences) at the National Cancer Institute (Office of Cancer Survivorship, 1999). No reports were found in which the effectiveness of the combination of risedronate, calcium, and vitamin D (administered together and at the current recommended levels for postmenopausal women) was studied, nor has the effectiveness of the addition of long term progressive strength/weight training exercises been evaluated in this at risk population of breast cancer survivors.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Postmenopausal Osteoporosis

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
249 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1 Strength/weight Training & Drug/Supplement
Arm Type
Experimental
Arm Description
Subjects in the G1 group receive 1200 mg of calcium and 400 IU of vitamin D supplements per day, 35 mg of risedronate per week and strength/weight training exercises for upper and lower extremities and the spine.
Arm Title
2 Drug/Supplement only
Arm Type
Experimental
Arm Description
Subjects in the G2 group receive the calcium, vitamin D, and risedronate, but do not participate in strength/weight training exercises.
Intervention Type
Other
Intervention Name(s)
Strength/weight Training & Drug/Supplement
Other Intervention Name(s)
Actonel
Intervention Description
G1 group receives 1200 mg of calcium and 400 IU of vitamin D supplements per day, 35 mg of risedronate per week and strength/weight training exercises for upper and lower extremities and the spine.
Intervention Type
Combination Product
Intervention Name(s)
Drug/Supplement only
Other Intervention Name(s)
Actonel
Intervention Description
G2 group receives the calcium, vitamin D, and risedronate, but do not participate in strength/weight training exercises.
Primary Outcome Measure Information:
Title
Bone Mineral Density
Description
Bone Mineral Density (gm/cm2) will be measured by Dual-Energy X-ray Absorptiometry (DEXA) of the hip, spine and forearm
Time Frame
at 12, 24, and 36 months
Secondary Outcome Measure Information:
Title
Muscle Strength
Description
Muscle Strength (peak torque/body weight at 60 degrees) will be assessed using BiodexTM Velocity Spectrum Evaluation (Medical Systems, Inc., 1993)
Time Frame
at baseline, 6, 12, 24, and 36 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
35 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: read, speak and understand English; be female; be between the ages of 35 and 75; have completed treatment (except tamoxifen) for stage 0, I or II breast cancer (i.e. surgery, chemotherapy, radiation) at least 6 months prior to admission to the study; be 1 year postmenopausal (12-months amenorrheic; subjects 55-years or younger with history of hysterectomy without oophorectomy must have it confirmed by two baseline measures of FSH >40 IU/ml); have a BMD T-score of -1.0 SD or lower at one or more sites (spine, hip or forearm); and have agreement of their primary care provider for participation in the study. Exclusion Criteria: have a recurrence of their breast cancer; currently take hormone replacement therapy, bisphosphonates, calcitonin, raloxifene, calcitriol, or glucocorticosteroids.; currently do strength/weight training exercises or high impact exercises (such as running, jumping rope, high impact aerobic dance, martial arts, volleyball, or basketball) two to three times weekly; have a body mass index (BMI) equal to or greater than 35; have serum calcium, creatinine or TSH (if on thyroid therapy) outside the normal limits; have active gastrointestinal problems such as dysphagia, esophageal disease, gastritis, duodenitis, or ulcers; have Paget=s disease; have renal disease (renal stones or serum creatinine levels greater than the upper normal limits); have a recent history of a spinal fracture (within the past 6 months); have features of an acute fracture on baseline spinal x-rays; have other concomitant conditions that prohibit strength/weight training exercises, calcium, or vitamin D intake.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nancy L Waltman, PhD, ARNP
Organizational Affiliation
University of Nebraska Medical Center, College of Nursing
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Nebraska Medical Center, College of Nursing
City
Kearney
State/Province
Nebraska
ZIP/Postal Code
68849-4510
Country
United States
Facility Name
University of Nebraska Medical Center, College of Nursing
City
Lincoln
State/Province
Nebraska
ZIP/Postal Code
68588-0220
Country
United States
Facility Name
University of Nebraska Medical Center, College of Nursing
City
Omaha
State/Province
Nebraska
ZIP/Postal Code
68198-5330
Country
United States
Facility Name
University of Nebraska Medical Center, College of Nursing
City
Scottsbluff
State/Province
Nebraska
ZIP/Postal Code
69361-4939
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
16999712
Citation
Twiss JJ, Gross GJ, Waltman NL, Ott CD, Lindsey AM. Health behaviors in breast cancer survivors experiencing bone loss. J Am Acad Nurse Pract. 2006 Oct;18(10):471-81. doi: 10.1111/j.1745-7599.2006.00165.x.
Results Reference
result
PubMed Identifier
16557117
Citation
Ott CD, Twiss JJ, Waltman NL, Gross GJ, Lindsey AM. Challenges of recruitment of breast cancer survivors to a randomized clinical trial for osteoporosis prevention. Cancer Nurs. 2006 Jan-Feb;29(1):21-31, quiz 32-3. doi: 10.1097/00002820-200601000-00004.
Results Reference
result

Learn more about this trial

Prevention of Osteoporosis in Breast Cancer Survivors

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