Progressive Muscle Relaxation for Pain and Quality of Life in Thyroid Cancer
PMRT-ThyCa
Effectiveness of Progressive Muscle Relaxation Technique on Pain and Quality of Life in Thyroid Cancer Patients: A Randomized Controlled Trial
1 other identifier
interventional
32
1 country
1
Brief Summary
Thyroid cancer patients often experience pain and reduced quality of life during chemotherapy. This randomized controlled trial will evaluate whether Progressive Muscle Relaxation (PMR) exercises, added to routine range-of-motion exercises, reduce pain and improve quality of life compared to range-of-motion exercises alone. Thirty-two thyroid cancer patients randomly assigned to either the PMR group or the control group. Pain measured by using the Numeric Pain Rating Scale (NPRS) and quality of life using the FACT-G questionnaire before and after a 4-5 day intervention. The study compared changes between groups.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jan 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
May 15, 2026
CompletedFirst Submitted
Initial submission to the registry
May 23, 2026
CompletedFirst Posted
Study publicly available on registry
June 3, 2026
CompletedJune 3, 2026
May 1, 2026
3 months
May 23, 2026
June 1, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Change in Pain Intensity
Pain intensity measured using the Numeric Pain Rating Scale (NPRS), an 11-point scale from 0 (no pain) to 10 (worst possible pain). Higher scores indicate worse pain.
Baseline (day 1) and post-intervention (day 4-5)
Change in Quality of Life
Quality of life measured using the Functional Assessment of Cancer Therapy - General (FACT-G), a 27-item questionnaire covering physical, social/family, emotional, and functional well-being. Higher scores indicate better quality of life.
Baseline (day 1) and post-intervention (day 4-5)
Study Arms (2)
PMR + ROM
EXPERIMENTALParticipants received once-daily Progressive Muscle Relaxation Technique (PMRT) plus range-of-motion (ROM) exercises for 4-5 consecutive days, 20-40 minutes per session.
ROM
ACTIVE COMPARATORParticipants received only gentle range-of-motion (ROM) and stretching exercises, once daily for 4-5 consecutive days, 20-40 minutes per session.
Interventions
Participants were guided through sequential tensing and relaxing of six muscle groups: head/neck, shoulders/upper back, arms/hands, lower back/hips, calves/thighs, and feet/toes. For each group, they inhaled deeply and tensed muscles for 10-20 seconds, then exhaled slowly while relaxing completely. Each session lasted 20-40 minutes, once daily for 4-5 consecutive days. Sessions were conducted by a trained physiotherapist in a quiet hospital room.
Participants performed gentle range-of-motion (ROM) and stretching exercises for the same muscle groups (head/neck, shoulders, arms, lower back, legs, feet), without the tensing-relaxation component of PMR. Each session lasted 20-40 minutes, once daily for 4-5 consecutive days, supervised by the same physiotherapist.
Eligibility Criteria
You may qualify if:
- Histologically confirmed thyroid cancer (Stage I-III)
- Age 30-50 years
- Moderate pain (NPRS score 3-7)
- Baseline FACT-G score ≥80%
- Undergoing chemotherapy (1-3 sessions completed)
- History of lobectomy or thyroidectomy
- Provided written informed consent
You may not qualify if:
- Comorbidities (cardiomyopathy, respiratory disorders, severe mental illness)
- Recent fractures or surgeries
- Unable to comprehend or follow instructions
- Currently practicing PMR or any other relaxation therapy
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
The University of Faisalabad
Faisalābad, Punjab Province, 3800, Pakistan
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Professor/ Head , Department of Rehabilitation Sciences
Study Record Dates
First Submitted
May 23, 2026
First Posted
June 3, 2026
Study Start
January 1, 2026
Primary Completion
April 1, 2026
Study Completion
May 15, 2026
Last Updated
June 3, 2026
Record last verified: 2026-05
Data Sharing
- IPD Sharing
- Will not share