Heavy Lifting Strength Training in Head and Neck Cancer Survivors (LIFTING)
Primary Purpose
Cancer of Head and Neck
Status
Completed
Phase
Phase 1
Locations
Canada
Study Type
Interventional
Intervention
Exercise Intervention
Sponsored by
About this trial
This is an interventional supportive care trial for Cancer of Head and Neck focused on measuring surgery, neck dissection, strength training, survivors, exercise
Eligibility Criteria
Inclusion Criteria:
- previously diagnosed with any subtype and stage of head and neck cancer
- at least one year post surgical neck dissection for head and neck cancer and showing full shoulder range of motion or recovery of the spinal accessory nerve
- adults ages 18 and older
- no unmanaged medical conditions, alcohol, and drug abuse
- approved for a heavy lifting strength training program by the treating surgeon and a certified exercise physiologist
- ability to understand and communicate in English
Exclusion Criteria:
- having comorbidities or uncontrolled medical conditions that their referred clinicians indicate as inappropriate to participate in exercise
Sites / Locations
- University of Alberta
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Exercise Intervention
Arm Description
Single exercise arm
Outcomes
Primary Outcome Measures
Recruitment Rate
Recruitment rate (with reasons for refusal).
Recruitment minimum: 15 participants Recruitment maximum: 20 participants Higher number= better and more data
Muscular Strength
Change in muscular strength from baseline to postintervention with be assessed using maximal strength tests.
Minimum: none Maximum: none Higher score= better strength
Program Adherence
Program adherence minimum: 80% Program adherence maximum: 100% Higher score= better adherence
Secondary Outcome Measures
Physical functioning
Assessed using the Neck Dissection Impairment Index (NDII) and maximum strength tests.
Minimum: 40 Maximum: 100 Higher score= worse impairment
Fear of cancer recurrence
Assessed using the Fear of Cancer Recurrence Inventory (FCRI)
Minimum: 0 Maximum: 36 Higher score= worse fear of cancer recurrence
Post Traumatic Growth after cancer
How cancer has changed an individual's life will be assessed using the Post Traumatic Growth Inventory (PTGI)
Minimum: 0 Maximum: 105 Higher score= better (positive) post traumatic growth transformation
Waist to hip ratio (body composition)
Assessed using waist to hip ratio (WHR) measure.
Minimum WHR: none Maximum WHR: none Higher score WHR= worse body composition
Anxiety
Assessed using the Spielberger State Trait Anxiety Inventory (STAI)
Minimum: 20 Maximum: 80 Higher score= worse anxiety
Fatigue
Assessed using the Functional Assessment of Chronic Illness Therapy-Fatigue (FACIT-F) questionnaire
Minimum: 0 Maximum: 52 Higher score=worse fatigue
Stress
Assessed using the Perceived Stress Scale (PSS)
Minimum: 0 Maximum: 56 Higher score=worse perceived stress
Shoulder Mobility
Changes in shoulder mobility
Minimum: 150 degrees (18-50 years); 130 degrees (over 50 years) Maximum: none Higher score= better mobility
Self-Esteem
Changes in level of self-esteem assessed using Rosenberg Self-Esteem (RSE) scale
Minimum: 10 Maximum: 40 Higher score= better self-esteem
Sleep
Changes in sleep patterns assessed using the insomnia severity index (ISI)
Minimum: 0 Maximum: 28 Higher score= worse insomnia
Motivation
Questions based on the theory of planned behaviour
Minimum: 7 Maximum: 35 Higher score= better motivation
Cancer specific quality of life
Assessed using the Functional Assessment of Cancer Therapy-Head and Neck (FACT-H&N Symptom Index)
Minimum: 0 Maximum: 40 Higher score= worse head and neck cancer symptoms
Cancer Symptom Burden
Assessed using the revised Edmonton Symptom Assessment System (ESAS-r)
Minimum: 0 Maximum: 100 Higher score= worse cancer symptoms
Height
Assessed using standing height without shoes.
Minimum height: none Maximum height: none Taller: not specifically better or worse
Weight
Assessed using a digital scale without shoes.
Minimum weight: none Maximum weight: none Higher weight: typically worse, but depends on other factors (ie. height, muscle mass, overall health status)
Full Information
NCT ID
NCT04554667
First Posted
September 11, 2020
Last Updated
September 2, 2022
Sponsor
University of Alberta
1. Study Identification
Unique Protocol Identification Number
NCT04554667
Brief Title
Heavy Lifting Strength Training in Head and Neck Cancer Survivors
Acronym
LIFTING
Official Title
Feasibility and Safety of Heavy Lifting Strength Training in Head and Neck Cancer Survivors Post-Surgical Neck Dissection
Study Type
Interventional
2. Study Status
Record Verification Date
September 2022
Overall Recruitment Status
Completed
Study Start Date
November 24, 2020 (Actual)
Primary Completion Date
July 31, 2022 (Actual)
Study Completion Date
July 31, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Alberta
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The LIFTING trial will examine the feasibility and safety of a heavy lifting strength training (HLST) program in head and neck cancer survivors (HNCS) at least 1 years post surgical neck dissection. The trial will determine whether this training style is safe and feasible in HNCS. Physical and psychosocial changes will also be reported.
Detailed Description
RATIONALE Despite improvements in treatments, HNCS still endure numerous acute and chronic side effects. Strength training has been shown to manage some of these side effects but most interventions have involved light-to-moderate resistance training programs. HLST may produce better outcomes but it is unknown if such a weight training program is feasible and safe for HNCS.
OBJECTIVE The primary aim of this proposed study is to examine the feasibility and safety of a HLST program in HNCS at least 1 year post-surgical neck dissection.
METHODS This single arm feasibility study will recruit 15-20 HNCS to complete the HLST program 2 times per week. The primary feasibility outcomes will include the eligibility rate (with reasons for ineligibility), recruitment rate (with reasons for refusal), 1 repetition maximum testing rate (with reasons for not completing the test), program adherence (including attendance, dose modifications, and progression), and follow-up assessment rate (with reasons for drop out). The primary efficacy outcome will be strength gains from baseline. Secondary efficacy outcomes will include physical functioning, quality of life, fear of cancer recurrence, pain, body composition, anxiety, fatigue, stress, shoulder mobility, self-esteem, sleep, and motivation to engage in a HLST program.
SIGNIFICANCE Weight training is an effective intervention in HNCS but the optimal weight training prescription is unknown. If heavy weight training is deemed safe and feasible in HNCS, it can be compared to light-to-moderate load weight training to determine if it is a better prescription for improving outcomes that are important to HNCS.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cancer of Head and Neck
Keywords
surgery, neck dissection, strength training, survivors, exercise
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Model Description
Single arm, safety and feasibility trial.
Masking
None (Open Label)
Allocation
N/A
Enrollment
9 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Exercise Intervention
Arm Type
Experimental
Arm Description
Single exercise arm
Intervention Type
Behavioral
Intervention Name(s)
Exercise Intervention
Intervention Description
Heavy Lifting Strength Training
Primary Outcome Measure Information:
Title
Recruitment Rate
Description
Recruitment rate (with reasons for refusal).
Recruitment minimum: 15 participants Recruitment maximum: 20 participants Higher number= better and more data
Time Frame
Over 12 weeks
Title
Muscular Strength
Description
Change in muscular strength from baseline to postintervention with be assessed using maximal strength tests.
Minimum: none Maximum: none Higher score= better strength
Time Frame
Changes from baseline to 12 weeks
Title
Program Adherence
Description
Program adherence minimum: 80% Program adherence maximum: 100% Higher score= better adherence
Time Frame
Over 12 weeks
Secondary Outcome Measure Information:
Title
Physical functioning
Description
Assessed using the Neck Dissection Impairment Index (NDII) and maximum strength tests.
Minimum: 40 Maximum: 100 Higher score= worse impairment
Time Frame
Changes from baseline to 12 weeks
Title
Fear of cancer recurrence
Description
Assessed using the Fear of Cancer Recurrence Inventory (FCRI)
Minimum: 0 Maximum: 36 Higher score= worse fear of cancer recurrence
Time Frame
Changes from baseline to 12 weeks
Title
Post Traumatic Growth after cancer
Description
How cancer has changed an individual's life will be assessed using the Post Traumatic Growth Inventory (PTGI)
Minimum: 0 Maximum: 105 Higher score= better (positive) post traumatic growth transformation
Time Frame
Changes from baseline to 12 weeks
Title
Waist to hip ratio (body composition)
Description
Assessed using waist to hip ratio (WHR) measure.
Minimum WHR: none Maximum WHR: none Higher score WHR= worse body composition
Time Frame
Changes from baseline to 12 weeks
Title
Anxiety
Description
Assessed using the Spielberger State Trait Anxiety Inventory (STAI)
Minimum: 20 Maximum: 80 Higher score= worse anxiety
Time Frame
Changes from baseline to 12 weeks
Title
Fatigue
Description
Assessed using the Functional Assessment of Chronic Illness Therapy-Fatigue (FACIT-F) questionnaire
Minimum: 0 Maximum: 52 Higher score=worse fatigue
Time Frame
Changes from baseline to 12 weeks
Title
Stress
Description
Assessed using the Perceived Stress Scale (PSS)
Minimum: 0 Maximum: 56 Higher score=worse perceived stress
Time Frame
Changes from baseline to 12 weeks
Title
Shoulder Mobility
Description
Changes in shoulder mobility
Minimum: 150 degrees (18-50 years); 130 degrees (over 50 years) Maximum: none Higher score= better mobility
Time Frame
Changes from baseline to 12 weeks
Title
Self-Esteem
Description
Changes in level of self-esteem assessed using Rosenberg Self-Esteem (RSE) scale
Minimum: 10 Maximum: 40 Higher score= better self-esteem
Time Frame
Changes from baseline to 12 weeks
Title
Sleep
Description
Changes in sleep patterns assessed using the insomnia severity index (ISI)
Minimum: 0 Maximum: 28 Higher score= worse insomnia
Time Frame
Changes from baseline to 12 weeks
Title
Motivation
Description
Questions based on the theory of planned behaviour
Minimum: 7 Maximum: 35 Higher score= better motivation
Time Frame
Changes from baseline to 12 weeks
Title
Cancer specific quality of life
Description
Assessed using the Functional Assessment of Cancer Therapy-Head and Neck (FACT-H&N Symptom Index)
Minimum: 0 Maximum: 40 Higher score= worse head and neck cancer symptoms
Time Frame
Changes from baseline to 12 weeks
Title
Cancer Symptom Burden
Description
Assessed using the revised Edmonton Symptom Assessment System (ESAS-r)
Minimum: 0 Maximum: 100 Higher score= worse cancer symptoms
Time Frame
Changes from baseline to 12 weeks
Title
Height
Description
Assessed using standing height without shoes.
Minimum height: none Maximum height: none Taller: not specifically better or worse
Time Frame
Changes from baseline to 12 weeks
Title
Weight
Description
Assessed using a digital scale without shoes.
Minimum weight: none Maximum weight: none Higher weight: typically worse, but depends on other factors (ie. height, muscle mass, overall health status)
Time Frame
Changes from baseline to 12 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
previously diagnosed with any subtype and stage of head and neck cancer
at least one year post surgical neck dissection for head and neck cancer and showing full shoulder range of motion or recovery of the spinal accessory nerve
adults ages 18 and older
no unmanaged medical conditions, alcohol, and drug abuse
approved for a heavy lifting strength training program by the treating surgeon and a certified exercise physiologist
ability to understand and communicate in English
Exclusion Criteria:
having comorbidities or uncontrolled medical conditions that their referred clinicians indicate as inappropriate to participate in exercise
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kerry S Courneya, PhD
Organizational Affiliation
University of Alberta
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Alberta
City
Edmonton
State/Province
Alberta
ZIP/Postal Code
T6G 2H9
Country
Canada
12. IPD Sharing Statement
Plan to Share IPD
No
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Heavy Lifting Strength Training in Head and Neck Cancer Survivors
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