Clinical trial · Interventional
Exercise Intervention for Cancer Survivors and Caregivers
Dyadic Exercise Intervention for Cancer Survivors and Caregivers
NCT01883635CI-TRIAL-00020818completedPhase 1Results postedClinicalTrials.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 the study is to see whether exercise can improve the health and well-being of cancer survivors. We also want to know about the health and well being of caregivers.
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 |
|---|---|---|---|
| Cancer | Malignant Neoplasm | ALIAS | 0.90 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Dyadic progressive walking and resistance exercise | Behavioral | — | UNRESOLVED |
| Survivor-only progressive walking and resistance exercise | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- ACTIVE_COMPARATOR
- label
- Individual Exercise Intervention
- description
- Survivor-only progressive walking and resistance exercise
- interventionNames
- Behavioral: Survivor-only progressive walking and resistance exercise
- type
- EXPERIMENTAL
- label
- Dyadic Exercise Intervention
- description
- Dyadic progressive walking and resistance exercise
- interventionNames
- Behavioral: Dyadic progressive walking and resistance exercise
Primary outcomes (1)
- measure
- Psychological Distress
- timeFrame
- Baseline to post-intervention (6 weeks later)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 21 Years
Show eligibility criteria text
Inclusion Criteria for Cancer Survivors: * Have a diagnosis of cancer (any cancer type excluding squamous and basal cell skin cancers) and have received surgery, chemotherapy, and/or radiation therapy within the last 1-12 months. * Have a functional capacity rating of 70 or greater on the Karnofsky Performance Scale or a rating of 1 or 0 on the ECOG scale when assessed by a medical oncologist (or physicians designee) following cancer treatments * Have a caregiver willing to participate int he study * Be able to read English * Be 21 years of age or older * Give written informed consent Inclusion Criteria for Caregivers: * Be nominated by a cancer survivor * Be able to read English * Be 21 years of age or older * Give written informed consent Exclusion Criteria: * have physical limitations (e.g. cardiorespiratory, orthopedic) contraindicating participation in a low to moderate intensity home based walking and progressive resistance program, as assessed by their medical oncologist, their primary care physician, and/or the study medical monitor. * For caregivers, be currently undergoing active treatment for cancer
References
Publications (0)
Data not yet available
No reference posted for this study.