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ParentPMR-PANCT07797608

Effect of Progressive Muscle Relaxation on Parental Anxiety

A study testing Progressive Muscle Relaxation in people with Parent and Anxiety, run by Akdeniz University.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Official record
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Trial summary

This randomized controlled trial aims to evaluate the effect of progressive muscle relaxation exercises on anxiety levels among parents who are the primary caregivers of children diagnosed with cancer and receiving inpatient treatment. Read more about this study

Who is it for?
Any ageHealthy volunteers can take part
Conditions the study is for
Parent, Anxiety, Cancer
What is being tested?
Progressive Muscle Relaxation
Could I receive a placebo?
No, everyone receives an active treatment
How many people
112 participants
Where
No sites listed yet
Study dates
15 Aug 2026to 20 Jul 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Who may be able to join

  • Being the parent and primary caregiver of a child diagnosed with cancer
  • The child having been diagnosed with cancer within the previous 12 months
  • The child currently receiving inpatient treatment in the study clinic
  • Being able to communicate without hearing or speech-related barriers
  • Being able to understand and answer the study questions
  • Providing written informed consent

Who cannot join

  • Not meeting any of the inclusion criteria
  • Withdrawing consent at any time

About this study

Official title: The Effect of Progressive Muscle Relaxation Exercises on Anxiety Among Parents of Children With Cancer: A Randomized Controlled Trial

This randomized controlled trial aims to evaluate the effect of progressive muscle relaxation exercises on anxiety levels among parents who are the primary caregivers of children diagnosed with cancer and receiving inpatient treatment. A total of 112 parents will be randomly assigned to either the intervention or control group. Parents in the intervention group will participate in researcher-led progressive muscle relaxation sessions. Anxiety will be assessed using the State Anxiety Inventory (STAI-I). The study will be conducted at the Pediatric Hematology-Oncology Clinic of Akdeniz University Hospital in Antalya, Türkiye.

Read the detailed description

Parents of children diagnosed with cancer may experience substantial anxiety throughout their child's diagnosis and treatment. Progressive muscle relaxation is a nonpharmacological technique involving the systematic tensing and relaxing of major muscle groups combined with deep breathing. Eligible parents will be randomly allocated in equal numbers to the intervention or control group using a computer-generated randomization sequence. The intervention will be delivered individually in a private clinical education room. Participants will progressively tense and relax the muscles of the face, neck, shoulders, chest, abdomen, legs, and feet. Each muscle group will be tensed for 5 seconds and relaxed for 10 seconds while participants practice deep breathing and visualize a wave of relaxation throughout the body. Anxiety will be assessed using the State Anxiety Inventory (STAI-I), and changes in anxiety scores will be compared between the groups.

Being tested
Progressive Muscle Relaxation
Keywords
Parent, Anxiety, Cancer, Progressive Muscle Relaxation, Nursing
Medical subject headings
Anxiety Disorders, Neoplasms

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Progressive Muscle RelaxationBehavioural

    Participants will receive routine clinical care and will not participate in progressive muscle relaxation sessions during the study period.

Study groups in NCT07797608
Study groupRoleWhat they receive
Progressive Muscle RelaxationExperimentalParticipants will receive two individual progressive muscle relaxation sessions in a private clinical education room over two weeks. Each session will last approximately 15 minutes and will be conducted once weekly.
Receives: Behavioral: Progressive Muscle Relaxation
ControlNo interventionParticipants in the control group will receive routine care provided by the clinic and will not participate in progressive muscle relaxation sessions during the study period.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in State Anxiety

    State anxiety will be measured using the State Anxiety subscale of the State-Trait Anxiety Inventory (STAI-S). The subscale contains 20 items and yields a total score ranging from 20 to 80. Higher scores indicate higher state anxiety.

    Measured: 2 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted1 Sep 2026
  2. Study start15 Aug 2026 (estimated)
  3. Primary completion20 Jul 2027 (estimated)
  4. Study completion20 Jul 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Supportive care
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Outcomes assessor
Enrolment
112 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07797608
Sponsor's protocol ID
TBAEK-976
Acronym
PMR-PA
Status last verified
Sep 2026
First submitted
10 Aug 2026
Last updated
9 Sep 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Progressive Muscle Relaxation in people with Parent and Anxiety, run by Akdeniz University.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 9 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in State Anxiety (time frame: 2 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Sep 2026.

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